Medical Director/Clinical Trial Physician - Neurology(FSP)

Thermo Fisher Scientific; Virginia (MN); Remote; USD 180,000 - 250,000; Full time

Job summary

A leading company in clinical research is seeking a Medical Director/Clinical Trial Physician specializing in neurology. This role includes overseeing clinical trials, ensuring compliance with regulatory requirements, and providing medical leadership. Candidates must be Medical Doctors with experience in clinical development, particularly in neurology. Competitive salary and benefits offered in a remote work environment with travel opportunities.

Benefits

Competitive salary

Bonuses

Healthcare

Career development opportunities

Qualifications

• Board certification preferred.
• Specialty in neurology with relevant research or clinical experience.
• 1-3 years industry experience in clinical development.

Responsibilities

• Provide medical leadership in study teams.
• Real-time medical monitoring to ensure study validity.
• Ensure study compliance with SOPs and GCP guidelines.

Skills

Excellent English communication skills

Understanding of NDA process

Leadership and interpersonal skills

Proactive problem-solving

Negotiation skills

Education

Medical Doctor or equivalent

Job description

Medical Director/Clinical Trial Physician - Neurology(FSP)

Join to apply for the Medical Director/Clinical Trial Physician - Neurology(FSP) role at Thermo Fisher Scientific.

Position posted 3 days ago — Be among the first 25 applicants.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office environment

About Thermo Fisher Scientific

We are committed to impactful work that improves health outcomes worldwide. Our clinical trials are conducted in over 100 countries, focusing on innovative research and development of life-changing therapies. Join us in making a difference.

Location

Based in the United States, preferably in Eastern or Central Time Zone. Fully remote with 10-20% travel (possible international).

Key Responsibilities

• Provide medical leadership in study teams, including protocol creation, review, and approval of clinical documents.
• Real-time medical monitoring to ensure study validity and participant safety.
• Interpret clinical data for regulatory submissions, publications, and reports.
• Serve as medical contact for stakeholders, including interactions with investigators, IRBs, and Health Authorities.
• Ensure study compliance with SOPs and GCP guidelines.
• Collaborate with cross-functional teams to address medical risks and issues.

Qualifications

• Medical Doctor or equivalent; board certification preferred.
• Specialty in neurology with relevant research or clinical experience.
• 1-3 years industry experience in clinical development within pharma, biotech, or CRO.
• Experience in pediatric neurology or neuromuscular diseases is highly preferred.

Skills & Abilities

• Excellent English communication skills.
• Understanding of NDA process and regulatory guidelines for adverse events.
• Leadership and interpersonal skills to guide study teams.
• Proactive problem-solving and negotiation skills.

Physical & Work Environment

• Office work with occasional travel.
• Ability to perform repetitive tasks, lift up to 20 lbs, and communicate effectively.
• Independent work with the ability to multitask and work under stress.

Benefits

Competitive salary, bonuses, healthcare, and career development opportunities. Join a culture of integrity, innovation, and involvement.