(Associate) Medical Director - Neurology

Thermo Fisher Scientific; United Kingdom; On-site; GBP 80,000 - 120,000; Full time

Job summary

Join a forward-thinking company as an Associate Medical Director in Neurology, where you'll lead clinical trials and ensure patient safety. This role offers the chance to make a significant impact in the pharmaceutical industry, working with a diverse team to deliver innovative therapies. You'll be responsible for medical oversight, protocol development, and collaboration across various departments. If you are passionate about advancing healthcare and have a strong background in neurology and clinical trials, this is the perfect opportunity to further your career in a dynamic and supportive environment.

Qualifications

• MD, MB/BS or equivalent degree with strong medical knowledge.
• Significant experience in pharmaceutical industry and clinical trials.

Responsibilities

• Provide medical leadership and support for clinical trials.
• Ensure compliance with all medical aspects and SOPs.
• Act as the medical point of contact for stakeholders.

Skills

Pharmaceutical Industry Experience

Clinical Trials

Medical Knowledge

Regulatory Guidelines Understanding

Communication Skills

Presentation Skills

Team Collaboration

Education

MD or MB/BS

Job description

(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 Thermo Fisher Scientific

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. Watch as our colleagues explain 5 reasons to work with us. 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. #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.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research and Science

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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