At a Glance
- Tasks: Lead clinical trials in neurology, ensuring safety and medical validity.
- Company: Join Thermo Fisher Scientific, a global leader in health and safety innovation.
- Benefits: Enjoy a full-time role with a supportive, inclusive culture and career growth opportunities.
- Other info: Be part of a mission-driven company that values integrity and innovation.
- Why this job: Make a real impact on global health while working with diverse teams.
- Qualifications: MD or equivalent, with experience in neurology and clinical trials required.
The predicted salary is between 72000 - 100000 £ per year.
(Associate) Medical Director - Neurology
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(Associate) Medical Director - Neurology
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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
Job 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
- MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Neurology patients in hospital practice.
- 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
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.
Seniority level
Seniority level
Director
Employment type
Employment type
Full-time
Job function
Job function
Health Care ProviderIndustries
Biotechnology
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(Associate) Medical Director - Neurology
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#J-18808-Ljbffr(Associate) Medical Director - Neurology employer: myGwork - LGBTQ+ Business Community
At Thermo Fisher Scientific, we pride ourselves on being an inclusive employer that values diversity and fosters a collaborative work culture. Our London office offers a dynamic environment where you can make a meaningful impact in the field of neurology while benefiting from extensive career development opportunities and a commitment to employee well-being. Join us to be part of a mission-driven team dedicated to making the world healthier, cleaner, and safer.
Contact Details:
myGwork - LGBTQ+ Business Community Recruitment 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, webinars, or local meetups to connect with potential colleagues and learn about the latest trends in clinical trials.
✨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 pharmacovigilance in detail. Be ready to share specific examples of how you've contributed to study protocols, safety evaluations, and interactions with regulatory bodies.
✨Tip Number 4
Showcase your communication and presentation skills by practising how you would explain complex medical concepts to non-medical stakeholders. This is crucial for the role, as you'll need to liaise with various teams and external partners.
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 pharmacovigilance and clinical trials makes you a perfect fit for Thermo Fisher Scientific. Be sure to mention your understanding of regulatory guidelines and your communication skills.
Showcase Relevant Skills:Highlight your significant experience within the pharmaceutical industry and your clinical knowledge. Mention your fluency in English and any experience with NDA submissions, as these are crucial for the role.
Proofread Your Application:Before submitting, carefully proofread your application materials. Ensure there are no spelling or grammatical errors, and that all information is clear and concise. A polished application reflects your attention to detail, which is vital for this role.
How to prepare for a job interview at myGwork - LGBTQ+ Business Community
✨Understand the Role Thoroughly
Before your 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. This will help you articulate how your experience aligns with the job.
✨Showcase Your Medical Expertise
Be prepared to discuss your medical background, particularly in neurology. Highlight any relevant clinical experience, especially with running trials or working with neurology patients. This will demonstrate your capability to provide medical leadership and support during clinical studies.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to handle real-world situations. Think of examples from your past experiences where you successfully navigated challenges in clinical trials or addressed safety concerns. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Emphasise Communication Skills
As a liaison between various stakeholders, strong communication is key. Be ready to discuss how you've effectively communicated complex medical information to diverse audiences, including investigators and regulatory bodies. This will show your ability to foster collaboration and ensure compliance throughout the study process.
