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- Tasks: Lead clinical trials, ensuring safety and medical validity while collaborating with study teams.
- Company: Join Thermo Fisher Scientific, a global leader in making the world healthier and safer.
- Benefits: Enjoy a supportive work environment with opportunities for career growth and impactful work.
- Why this job: Make a real difference in healthcare by contributing to life-changing therapies and clinical research.
- Qualifications: MD or equivalent degree with experience in Neurology and clinical trials is essential.
- Other info: Be part of an inclusive team that values diverse perspectives and backgrounds.
The predicted salary is between 72000 - 108000 £ per year.
Join to apply for the (Associate) Medical Director - Neurology role at myGwork - LGBTQ+ Business Community. This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.
Work Schedule: Standard (Mon-Fri)
Environmental Conditions: Office
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. As one team of 100,000+ 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.
Apply today!
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.
(Associate) Medical Director - Neurology employer: Job Traffic
Contact Detail:
Job Traffic Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land (Associate) Medical Director - Neurology
✨Tip Number 1
Network with professionals in the neurology and pharmaceutical fields. Attend industry conferences or webinars where you can meet potential colleagues and learn more about the latest trends in clinical trials and pharmacovigilance.
✨Tip Number 2
Familiarise yourself with Thermo Fisher Scientific's mission and values. Understanding their commitment to making the world healthier, cleaner, and safer will help you align your discussions and demonstrate your passion for their work during interviews.
✨Tip Number 3
Prepare to discuss your experience with clinical trials and regulatory guidelines. Be ready to provide specific examples of how you've contributed to study protocols or managed medical risks in previous roles, as this will showcase your expertise.
✨Tip Number 4
Engage with the LGBTQ+ community and organisations like myGwork. This not only shows your support for inclusivity but also helps you connect with others who may have insights or advice on navigating the application process at Thermo Fisher Scientific.
We think you need these skills to ace (Associate) Medical Director - Neurology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in neurology and clinical trials. Emphasise any leadership roles you've held and specific projects that align with the responsibilities of the (Associate) Medical Director position.
Craft a Compelling Cover Letter: In your cover letter, express your passion for improving health outcomes and how your background in pharmaceutical medicine makes you a strong candidate. Mention your understanding of regulatory guidelines and your experience with NDA submissions.
Showcase Communication Skills: Since strong communication and presentation skills are crucial for this role, provide examples in your application of how you've effectively communicated complex medical information to diverse audiences.
Highlight Team Collaboration: Discuss your experience working within cross-functional teams. Provide specific examples of how you've collaborated with different departments to ensure study compliance and address medical risks during clinical trials.
How to prepare for a job interview at Job Traffic
✨Understand the Role Thoroughly
Before the interview, make sure you have a solid grasp of the responsibilities and expectations of the (Associate) Medical Director role. Familiarise yourself with clinical trial protocols, pharmacovigilance, and the specific challenges faced in neurology to demonstrate your expertise.
✨Showcase Your Experience
Be prepared to discuss your previous experience in clinical trials and pharmaceutical medicine. Highlight specific examples where you've successfully led study teams or managed medical monitoring, as this will illustrate your capability to handle the demands of the position.
✨Communicate Effectively
Strong communication skills are essential for this role. Practice articulating complex medical concepts clearly and concisely, as you'll need to interact with various stakeholders, including investigators and regulatory bodies. Consider preparing a few key points about your communication style and how it has benefited past projects.
✨Demonstrate Team Collaboration
The role requires close collaboration with cross-functional teams. Be ready to share examples of how you've worked effectively within a team setting, resolved conflicts, or contributed to a positive team dynamic. This will show that you can thrive in a collaborative environment.
