Job Title | Location | Description | Posted** |
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Strategic Enterprise Account Executive
anaplan |
Remote-Denmark, Denmark
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At Anaplan we are a team of innovators focused on optimizing business decision-making through our leading AI-infused scenario planning and analysis platform so our customers can outpace their competition and the market. What unites Anaplanners across teams and geographies is our collective commitment to our customers’ success and to our Winning Culture. Our customers rank among the who’s who in the Fortune 50. Coca-Cola LinkedIn Adobe LVMH and Bayer are just a few of the 2400+ global companies who rely on our best-in-class platform. Our Winning Culture is the engine that drives our teams of innovators. We champion diversity of thought and ideas we behave like leaders regardless of title we are committed to achieving ambitious goals and we love celebrating our wins – big and small. Supported by operating principles of being strategy-led values-based and disciplined in execution you’ll be inspired connected developed and rewarded here. Everything that makes you unique is welcome join us and let’s build what’s next - together!Anaplan is seeking a highly ambitious Enterprise Account Executive to manage and grow our Enterprise and Mid-Market business in Denmark. In this role you will build on this success to ensure our clients expand the value they gain from Anaplan across their businesses and together with our partners you will drive and execute campaigns to win new customers. In this role you will be selling business value and transformational potential from sophisticated technology solutions to stakeholders across Finance Supply Chain Operations and HR. Our sales team is helping industry leaders understand the impact of Anaplan products and how our connected planning solution is ending siloed decision-making. You will help our customers achieve their immediate business goals while setting their business up for the future. This role will be a catalyst to Anaplan’s continued growth while leading digital transformation. Reporting directly to the RVP of Sales. Your Impact Engaging with targeted prospects and clients to identify broken business processes and position Anaplan’s unique ability to solve the problem Build Anaplan’s business value throughout the selling engagement. Navigating sophisticated prospect environments to align the prospect around the Anaplan solution Conduct highly effective presentations from Director through SVP and key C-suite level decision makers including CFOs CROs and senior leaders in supply chain workforce and other business functions Develop customers and own opportunity management start-to-finish across multiple customer targets and functions Apply Anaplan’s value-based selling methodology and tools to run sales processes and accurately forecast business Employ outstanding account leadership skills to identify account expansion opportunities by cross-selling and up-selling opportunities within targeted accounts Perform strategic sales planning leading to accurate forecasting of the business Work with cross-functional members of Sales Development Reps Marketing Solution Consultants and the Customer Success teams. Your Qualifications Consultative sales experience into enterprise and mid-enterprise companies ideally in SaaS solutions (but not required) Shown success selling into Vice President / Senior Vice President buyers Track record of overachieving sales quota & targets including demonstrated history of multiple high six-figure annual contract value (ACV) deals (services and/or software) Demonstrated network in your industry territory with a mix of some customers and implementation partners Demonstrated experience with sophisticated partner & internal team organizations Domain understanding (Supply Chain FP&A Workforce Planning & Sales) and knowledge of how these functions plan process work and make decisions Strong demonstrated opportunity management practices (e.g. sales process qualification executive presentation skills quote presentation and negotiation) and ability to balance multiple (3-5) opportunities at once. Preferred Skills Experience with Outreach SFDC LinkedIn Sales Navigator a plus Account Planning experience Altify MEDDPICC Miller Heiman. #LI-Remote Our Commitment to Diversity Equity Inclusion and Belonging (DEIB) We believe attracting and retaining the best talent and fostering an inclusive culture strengthens our business. DEIB improves our workforce enhances trust with our partners and customers and drives business success. Build your career in a place where diversity equity inclusion and belonging aren’t just words on paper – this is what drives our innovation it’s how we connect and it contributes to what makes us a market leader. We believe in a hiring and working environment where all people are respected and valued regardless of gender identity or expression sexual orientation religion ethnicity age neurodiversity disability status citizenship or any other aspect which makes people unique. We hire you for who you are and we want you to bring your authentic self to work every day! We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process perform essential job functions and receive equitable benefits and all privileges of employment. Please contact us to request accommodation. Fraud Recruitment Disclaimer It has come to our attention that fraudulent and fictitious job opportunities are being circulated on the Internet. Prospective candidates are being contacted by certain individuals mainly through telephone calls emails and correspondence claiming they are representatives of Anaplan. The main purpose of these correspondences and announcements is to obtain privileged information from individuals. Anaplan does not: Extend offers to candidates without an extensive interview process with a member of our recruitment team and a hiring manager via video or in person. Send job offers via email. All offers are first extended verbally by a member of our internal recruitment team whenever possible and then followed up via written communication. All emails from Anaplan would come from an @anaplan.com email address. Should you have any doubts about the authenticity of an email letter or telephone communication purportedly from for or on behalf of Anaplan please send an email to people@anaplan.com before taking any further action in relation to the correspondence.
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Supply Chain Manager
Happy Koala LLC |
Remote Denmark
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Happy Mammoth is a fast-growing natural food tech business selling across Australia Europe and the United States. We specialize in formulating producing and marketing gut digestive and microbiome health foods and natural supplements designed to help our clients make long-lasting positive health changes and start living very full lives again. What You Get: Competitive salary in USD Work remotely from anywhere in the world such as your home co-working space or cafe Lots of variation to keep the day-to-day exciting Free access to books courses and anything else that helps improve your skill set We are looking to hire a Supply Chain Manager to help us keep growing. If you're hard-working and dedicated Happy Mammoth is an ideal place to get ahead. Apply today! Qualifications & experience Must have 5 years’ experience in manufacturing industries (pref. in food). Must have 3 years’ experience in Supply Chain or similar role Strong industry knowledge Strong communication and interpersonal skills Exceptional organisation and negotiation skills Tasks & responsibilities Integral part of the entire process from R&D to finished product Responsible for overseeing internal processes and procedures within Supply Chain whilst liaising with Quality Assurance Finance and Operations Manager Sourcing negotiating procuring ingredients – blanket orders forecasts meeting budgets Managing of accurate inventory levels based on analytical data – working with internal and external partners to maximise profit Managing co-ordinating and planning production schedules lead times production shifts – minimising OOS. Managing and co-ordinating logistics – planning and booking freight liaising with warehouse to ensure deliveries and lead times are met Maintaining relationships of all third-party suppliers (packaging ingredients) distributors and key accounts Building & Maintaining relationships of all third-party suppliers (packaging ingredients) distributors and key accounts Leading Team of Production Coordinators Working closely with Head of Finance to drive Production Team in the most effective way ensuring it’s supporting business objectives and profitability. TRHIvbM3r0
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Medical Writer - In Vitro Diagnostics (IVD)
Agilent Technologies |
Remote Denmark
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Job Description - Agilent Technologies is seeking an experienced Medical Writer to join our Global Clinical Affairs team in Glostrup (Copenhagen) within the Organization of Chief Medical Officer (OCMO). This role plays a critical part in supporting our medical diagnostic portfolio ensuring compliance with the EU In Vitro Diagnostic Regulation (IVDR) 2017/746. As a key contributor you will be responsible for compiling and interpreting clinical performance data for all CE-marked products. Your work will support regulatory submissions and ongoing compliance efforts. You will collaborate closely with cross-functional teams including Research & Development Quality Assurance Regulatory Affairs and other internal partners. Key Responsibilities: Author Clinical Performance Reports for CE-marked products in compliance with IVDR (EU) 2017/746 as well as clinical research reports abstracts and publications Support the preparation and maintenance of technical documentation for regulatory submissions and audits. Conduct systematic literature searches to support IVDR documentation post-market surveillance and regulatory submissions. Analyze and trend External Quality Assessment (EQA) performance data. Research internal controlled documents and Instructions for Use (IFUs) for existing clinical performance data. Collaborate with internal stakeholders to compile documentation required under EU IVDR. Work with subject matter experts to ensure scientific accuracy and strategic alignment. Contribute to clinical process development and author Standard Operating Procedures (SOPs). Qualifications We are looking for an experienced individual with the following background: University degree at least 2 years industry experience in technical/science or medical writing capacity Strong understanding of Good Clinical Practice (GCP) and regulatory documentation standards (knowledge of IVDR regulations will be considered a plus). Ability to conduct and synthesize systematic literature reviews. Excellent written communication skills with attention to scientific detail. Ability to work independently and collaboratively in a cross-functional environment. We offer: Permanent Contract and Core global benefits including the Agilent Result Bonus and Stock Purchase Plan. An exciting workday with many challenges where you have the opportunity to influence processes and the way we work. An inspiring work environment with dedicated and competent colleagues - humor and smiles are part of everyday life! A good balance between work and private life. We will make sure you get all the training and development opportunities to become the best in your field! Additional Details This job has a full time weekly schedule. It includes the option to work remotely. Our pay ranges are determined by role level and location. Within the range individual pay is determined by work location and additional factors including job-related skills experience and relevant education or training. During the hiring process a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other protected categories under all applicable laws.Travel Required: NoShift: DayDuration: - No End DateJob Function: - Medical/Clinical
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Data Analyst
Happy Koala LLC |
Remote Denmark
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About Happy Mammoth: Happy Mammoth is a high-growth e-commerce company dedicated to empowering women’s health through natural science-backed supplements focused on gut digestive and hormonal wellness. As a performance-driven company we are passionate about making a meaningful lasting impact on our customers' lives. You can learn more about us at https://happymammoth.com/. Before you dive deeper please note the following key points: This is a fully remote contractor role available full-time. The role requires availability during EU hours (GMT). At Happy Mammoth you can expect: A strong salary package. A welcoming and nurturing work environment with colleagues from around the world. A fast-paced dynamic and non-corporate atmosphere where adaptability is key. The chance to be part of our exciting global expansion journey. Flexible working hours. Free access to courses books and Masterminds Opportunities for professional growth and development. Job Summary: As a Data Analyst at Happy Mammoth you’ll be at the heart of our data-driven efforts. Your insights will directly influence our strategies to optimize customer acquisition retention and lifetime value. In this role you’ll dive into customer behavior analyze marketing performance and provide actionable insights that drive our direct-response and B2C marketing initiatives. Responsibilities: Collect analyze and interpret data to uncover trends patterns and insights that inform our business strategies. Build maintain and automate dashboards and reports to track KPIs including ROAS CPA conversion rates CLTV and customer retention metrics. Work closely with cross-functional teams such as marketing product and finance to provide data-driven insights that support campaign performance and strategic marketing decisions. Provide ad hoc analysis to address specific business questions. Ensure data quality and accuracy by regularly validating and cleansing datasets. Communicate findings effectively to both technical and non-technical stakeholders through reports presentations and storytelling. Qualifications: Proven experience in data analysis preferably with a focus on e-commerce. Proficiency in SQL and Excel. Proven experience in data visualization tools (e.g. Looker Data Studio Looker Power BI or similar). Hands-on experience with cloud-based data warehouses and architectures (familiarity with Google BigQuery is a strong asset). Strong analytical skills and attention to detail. Effective communicator with the ability to convey complex data insights clearly. What will set you apart: You have a genuine hunger for success in all parts of your life You thrive taking action taking responsibility and getting things done before deadlines You’re able to self-manage based upon the overall scope and work required You’re able to diagnose and solve technical problems quickly You're able to work as part of a team and actively contribute to conversations A willingness to learn and grow with the business CVs should be in English RKvIFjge8p
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Medical Writer - In Vitro Diagnostics (IVD)
Agilent Technologies |
Remote Denmark
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Job Description - Agilent Technologies is seeking an experienced Medical Writer to join our Global Clinical Affairs team in Glostrup (Copenhagen) within the Organization of Chief Medical Officer (OCMO). This role plays a critical part in supporting our medical diagnostic portfolio ensuring compliance with the EU In Vitro Diagnostic Regulation (IVDR) 2017/746. As a key contributor you will be responsible for compiling and interpreting clinical performance data for all CE-marked products. Your work will support regulatory submissions and ongoing compliance efforts. You will collaborate closely with cross-functional teams including Research & Development Quality Assurance Regulatory Affairs and other internal partners. Key Responsibilities: Author Clinical Performance Reports for CE-marked products in compliance with IVDR (EU) 2017/746 as well as clinical research reports abstracts and publications Support the preparation and maintenance of technical documentation for regulatory submissions and audits. Conduct systematic literature searches to support IVDR documentation post-market surveillance and regulatory submissions. Analyze and trend External Quality Assessment (EQA) performance data. Research internal controlled documents and Instructions for Use (IFUs) for existing clinical performance data. Collaborate with internal stakeholders to compile documentation required under EU IVDR. Work with subject matter experts to ensure scientific accuracy and strategic alignment. Contribute to clinical process development and author Standard Operating Procedures (SOPs). Qualifications We are looking for an experienced individual with the following background: Master's degree or advanced degree in pharmaceutical medical or relevant biomedical science fields. 4+ years of experience in clinical research medical writing or clinical science in the medical device and/or pharmaceutical industry Strong understanding of IVDR regulations Good Clinical Practice (GCP) and regulatory documentation standards. Ability to conduct and synthesize systematic literature reviews. Excellent written communication skills with attention to scientific detail. Ability to work independently and collaboratively in a cross-functional environment. We offer: Permanent Contract and Core global benefits including the Agilent Result Bonus and Stock Purchase Plan. An exciting workday with many challenges where you have the opportunity to influence processes and the way we work. An inspiring work environment with dedicated and competent colleagues - humor and smiles are part of everyday life! A good balance between work and private life. We will make sure you get all the training and development opportunities to become the best in your field! Additional Details This job has a full time weekly schedule. It includes the option to work remotely. Our pay ranges are determined by role level and location. Within the range individual pay is determined by work location and additional factors including job-related skills experience and relevant education or training. During the hiring process a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other protected categories under all applicable laws.Travel Required: NoShift: DayDuration: - No End DateJob Function: - Medical/Clinical
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Group Internal Auditor - Manufacturing Multinational - Clear Career Trajectory
Hanami International |
Remote Denmark
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Title: Group Internal Auditor Location: Denmark (Remote) Industry: Manufacturing / Global Production Function: Internal Audit Overview Our client a global leader in the production industry is looking for an Auditor to join their expanding internal audit function. This role offers outstanding international exposure and clear long-term development opportunities across multiple functions. Key Responsibilities Conduct operational and financial audits across global locations Report directly to the Group Head of Internal Audit Identify risks and provide practical recommendations to enhance internal controls Collaborate with senior stakeholders across multiple regions and functions Travel internationally up to 50-60% in the first two years What’s on Offer Remote-first position based anywhere in Ireland Exposure to a global business with sites in the US Europe Middle East and Asia Career progression into Finance Project Management and other business areas (e.g. USA Dubai France) Support for certifications (CIA CISA CFE) Flexible work environment and strong focus on professional development Your Profile Background in external audit (Big 4 or similar) ideally with international client exposure Accounting qualification Strong understanding of internal controls risk and audit methodology Fluent in English and Danish Excellent communication and stakeholder management skills Willingness to travel globally Apply This is a unique opportunity to accelerate your career in a high-performing global environment. Apply today for a confidential conversation.
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Sales Director - Energy sector
vHive |
Remote Denmark
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"vHive is seeking a highly motivated and hands-on Director of Sales to drive the expansion of our Energy business. This role is for a proven sales professional who will be responsible for a full sales cycle from prospecting to closing with a focus on selling our digital twin platform and inspection solutions to owners of large-scale wind and solar farms. The ideal candidate has deep domain expertise and a passion for technology that solves real-world operational challenges. Responsibilities: Sales Cycle Ownership: Own and manage the entire sales cycle from initial qualification and discovery to negotiation and closing. Targeting & Prospecting: Actively identify and pursue new opportunities with owners and operators of large-scale wind and solar farms in [Europe or North America.. Domain Expertise: Leverage a deep understanding of the renewable energy ecosystem including the customer's operational mindset business cases and decision-making criteria. Problem-Solving: Uncover customer pain points and optimization potential then articulate specific technical and commercial solutions enabled by the vHive platform. Hands-on Engagement: Plan and deliver hands-on product demonstrations ( and including flying drones!) and Proof of Value (POV) projects that clearly differentiate vHive from competitors. Market Insight: Stay on top of market trends and competitive dynamics within the renewable energy sector and communicate these insights to the marketing and product teams. Cross-Functional Collaboration: Lead the RFX proposal process and collaborate with multidisciplinary project teams to ensure all deliverables meet customer needs. Product Feedback: Inform the product management and technical teams on market requirements customer needs and potential product adaptations. Requirements: Experience: 5+ years of proven direct sales experience within the renewable energy sector (wind or solar) with a track record of selling to large-scale enterprise customers. Ecosystem Knowledge: Possesses a strong understanding of the wind and solar farm ecosystem including key stakeholders asset management workflows and operational challenges. Hunter Mentality: A results-driven ""hunter"" mindset with enormous enthusiasm and perseverance to identify and close new business opportunities. Entrepreneurial Problem Solving: A hands-on creative problem-solver who can take control of the sales process and build trust with customers. Flexibility & Adaptability: Possesses a flexible and innovative mindset with the ability to navigate complex customer environments and pivot strategies as needed. Communication: Strong written and verbal communication skills with the ability to articulate complex technical and commercial concepts to a global multi-cultural audience. Education: A degree in engineering finance or economics is preferred. Location: Based in Europe or North America near a major travel hub with willingness to travel."
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Sales Manager, Nordics
unger |
Denmark (Remote)
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Sales Manager Nordics Exciting Opportunity in a Great Company! Are you ready to join a growing business with a dynamic culture? Unger a market leader and leading brand in high-quality cleaning products is looking for a dedicated professional to join our team. With over 60 years of international experience Unger manufactures innovative and unique cleaning tools that help professionals improve cleanliness and health in buildings. Our main EMEA office and production facility is in Germany and our headquarters in the United States. Our products are successfully sold in over 80 countries. Our Culture: At Unger we believe in fostering a collaborative and inclusive work environment where every team member is valued. We pride ourselves on our innovative spirit and our commitment to excellence. Our culture is built on the principles of accountability responsibility and mutual respect. We encourage our employees to take the initiative drive success and make a difference with their unique skills and perspectives. Our dynamic team is passionate about what they do and we support each other in achieving both personal and professional growth. Your Responsibilities: · Must reside in Denmark · Responsible for the sales region of Denmark Sweden Finland and Norway · Support and advise current distribution partners and their sales teams · Maintain organic and develop new profitable customers in the assigned countries · Demonstrate products at customer sites promote new product innovations · Provide training to customers and prospects · Key Account Management · Develop advise and train end-users · Develop and execute new sales strategies following the annual sales plan · Forecast revenues by customers and products for the individual territories · Active collaboration with internaldepartments · Participate in international meetings and exhibitions · Reporting to the Country Manager BNL & Nordics · Management: Lead the Regional Sales Manager · Able to travel intensely within Scandinavia Your Profile: · Completed vocational degree or University Degree in a related field · Several years of experience preferably from the cleaning industry with a successful B2B track record in selling quality and added value products · Experience in Key Account Management helpful and preferred · Experienced in explaining and training technical and complex products · Commitment responsibility & accountability high degree of self-motivation self-confidence strong customer and service orientation · Competent and high emotional intelligence to deal with different customers · Structured and analytical in work habits and time management · Very good communication skills business acumen negotiation skills and “hands-on” mentality · Ability to travel frequently We look forward to receiving your application documents including your CV salary expectations and possible start date.
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Senior Enterprise Account Manager
AVEVA |
Remote Denmark
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AVEVA is a global leader in industrial software. Our cutting-edge solutions are used by thousands of enterprises to deliver the essentials of life – such as energy infrastructure chemicals and minerals – safely efficiently and more sustainably. We’re the first software business in the world to have our sustainability targets validated by the SBTi and we’ve been recognized for the transparency and ambition of our commitment to diversity equity and inclusion. We’ve also recently been named as one of the world’s most innovative companies. If you’re a curious and collaborative person who wants to make a big impact through technology then we want to hear from you! Find out more at AVEVA Careers. For more information about our privacy policy and how to manage cookies visit our Privacy Policy. Job title: Senior Enterprise Account Manager Location: Denmark Remote Employment Type: Full Time The Job The Senior Enterprise Account Manager will be responsible for developing and managing strategic relationships with major Nordics companies. This role involves driving business growth by selling AVEVA’s suite of products and services identifying new opportunities and ensuring customer satisfaction. Key responsibilities Account Management: Develop and maintain strong relationships with key stakeholders within the client organization. Sales Strategy: Implement and execute detailed account plans to achieve revenue targets and forecasts. Business Development: Identify and pursue new business opportunities within the account to create pipeline and drive growth. Customer Engagement: Act as the primary point of contact for the client addressing their needs and ensuring satisfaction. Solution and Value Selling: Collaborate with internal teams to deliver customized solutions that meet the client's requirements and drive value. Market Expertise: Stay informed on industry trends customer needs and competitive products to effectively position AVEVA’s solutions. Reporting: Manage the sales pipeline using Salesforce and provide regular updates on account performance. Coordination: Coordinate AVEVA’s touch points globally including local/regional sales account management field service customer technical support industry and marketing principals partners and back-office areas such as purchasing and finance for named accounts. Customer Satisfaction: Strive for high customer satisfaction and experience from a globally consistent AVEVA look feel and performance focused on value generation and sustainment. Essential requirements Proven experience in account management or sales preferably within the Energy and Process industries. Track record in building executive-level relationships within global energy organizations sales of complex B2B enterprise software leading virtual account teams and orchestrating complex global engagements. Strong communication negotiation and relationship-building skills. Deep trusted advisor status working with a customer organization within the energy vertical. Familiarity with AVEVA’s products and services as well as the Energy/Oil and Gas industry. Willingness to travel regionally and occasionally internationally (approx. 30-40% PA). Desired Skills Leveraging curiosity to understand the customer’s business goals issues and priorities and how AVEVA can be an influential partner. The Senior Enterprise Account Manager will manage 3-4 accounts. These are large complex accounts with growth potential requiring a growth mindset and aspiration to create deep customer relationships at all levels within their organisation and understanding of their business. This role requires the ability to discover new opportunities for AVEVA’s solutions and platform across our entire portfolio. Working with the customer to explore and build a business case for investment with AVEVA impacting supporting the growth of the business. You will become a trusted advisor to your customer as such you will have sound commercial and analytical skills to help identify market trends and opportunities for your nominated accounts refining business and account plans to exploit such opportunities. Commerical at AVEVA Our Commercial team comprised of over 2000 dedicated colleagues is the backbone of our customer relationships and business growth. From industry experts and solution architects to sales support success managers and business operations everyone shares a common goal: to deeply understand our customers' needs and deliver tailored solutions. If you're passionate about driving growth tackling complex business challenges and fostering strong customer relationships you'll find success and fulfilment in our Commercial team. AVEVA requires all successful applicants to undergo and pass a comprehensive background check before they start employment. Background checks will be conducted in accordance with local laws and may subject to those laws include proof of educational attainment employment history verification proof of work authorization criminal records identity verification credit check. Certain positions dealing with sensitive and/or third party personal data may involve additional background check criteria. AVEVA is an Equal Opportunity Employer. We are committed to being an exemplary employer with an inclusive culture developing a workplace environment where all our employees are treated with dignity and respect. We value diversity and the expertise that people from different backgrounds bring to our business. Come and join AVEVA to create the transformative technology that enables our customers to engineer a better world.
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(Associate) Medical Director - Neurology
Thermo Fisher Scientific |
Remote Denmark
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Work Schedule Standard (Mon-Fri)Environmental Conditions OfficeJob Description At Thermo Fisher Scientific you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Discover Impactful Work: The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department. A day in the Life: Provide medical leadership to the study teams including creating clinical trial protocols while implementing the latest scientific information contribute to site selection involved in review and approval of study protocols and amendments Clinical Study Reports (CSRs) Informed Consent Forms (ICFs) Case Report Forms (CRFs) protocol deviation decisions and other clinical documents as required for the conduct of clinical trials Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead During initial review of protocol consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions’ dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD part of Thermo Fisher Scientific internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed answer questions of IRBs and Health Authorities prepare and present material to the study executive and independent safety committee if applicable medical training of site staff at Investigator meetings CRA training in new indications Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP Closely collaborate with the cross functional study team members in order for medical risks issues and results to be clear to all involved parties Education MD MB/BS or equivalent degree and strong medical knowledge shown clinical experience running Neurology patients in hospital practice. Knowledge Skills Abilities Significant experience within pharmaceutical industry clinical trials and pharmaceutical medicine is critically important Is fluent in spoken and written English Shown understanding and experience with NDA submission process. Shown understanding of regulatory guidelines for adverse event reporting Strong communication & presentation skills and is a strong teammate Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000+ colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory with PPD part of Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued. Apply today! http://jobs.thermofisher.com Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.
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