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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Medical Director - Clinical Trial Physician, Neurology

Biology & BiotechConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A Medical Doctor or equivalent degree is required.
  • Specialty education, such as residency or fellowship, in neurology is required, accompanied by patient treatment and/or research experience.
  • One to three years of industry experience in clinical development at a pharmaceutical, biotech, or contract research organization is required.
  • Excellent written and spoken English is required, as is the ability to travel.
  • Understanding and experience with the New Drug Application submission process is required.
  • Understanding of regulatory guidelines for adverse event reporting is required.
  • The candidate must demonstrate interpersonal skills to lead a study team, recognize individual expert competencies, provide medical advice and evaluations, and exercise judgment about issues requiring immediate escalation.
  • The candidate must be able to work with cross-functional team members to make study plans, status, risks, issues, and results clear.
  • The candidate must be legally authorized to work in the United States or Canada without sponsorship.
  • The candidate must pass a comprehensive background check, including drug screening where applicable.
  • The candidate must be able to work Eastern Standard Time hours, with an East Coast time zone preferred.
  • The role requires frequent stationary work for six to eight hours per day, frequent mobility, occasional driving to site locations, and occasional domestic and international travel.
  • The role requires repetitive hand movements and occasional crouching, stooping, bending, and twisting of the upper body and neck.
  • The role requires light to moderate lifting and carrying of objects, including luggage and a laptop, up to 15–20 pounds.
  • The role requires using computer software, communicating and understanding spoken information, interacting with diverse groups, working independently with little guidance, planning work schedules, concentrating intensely, multitasking, and performing under stress.

Responsibilities

  • Provide medical leadership to study teams, including creating clinical trial protocols that implement current scientific information and contributing to site selection.
  • Contribute to the review and approval of study protocols and amendments, Clinical Study Reports, Informed Consent Forms, Case Report Forms, protocol deviation decisions, and other clinical documents needed to conduct clinical trials.
  • Conduct real-time medical monitoring of clinical studies, ensuring the medical validity of each primary endpoint and study-subject safety, identifying medical issues early, and proactively escalating and correcting issues in consultation with the Global Medical Indication Lead.
  • Interpret clinical trial data for regulatory documents, including Clinical Study Reports, Investigational New Drug applications, Annual Reports, New Drug Applications, and Marketing Authorisation Applications, as well as manuscripts and other publications, in consultation with the Indication Lead.
  • Serve as the medical point of contact for internal and external stakeholders; interact with investigators as needed; answer questions from institutional review boards and health authorities; and prepare and present material to the study executive and independent safety committee when applicable.
  • Provide medical training to site staff at investigator meetings and train clinical research associates in new indications.
  • Ensure compliance with all medical aspects of studies by understanding and applying relevant standard operating procedures and Good Clinical Practice.
  • Collaborate closely with cross-functional study team members so that medical risks, issues, and results are clear to all involved parties.
  • When multiple physicians work on a protocol, serve as primus inter pares when appointed, harmonizing answers to site, institutional review board, and regulatory authority questions, as well as eligibility and protocol deviation decisions.

Desired Qualifications

  • Board certification(s) are preferred.
  • Expertise in pediatric neurology or neuromuscular diseases is highly preferred.
  • An East Coast time zone location is preferred.

About the Company

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Thermo Fisher Scientific makes and sells the instruments, chemicals, consumables and lab services that drug companies, hospitals, universities and industrial labs use for research, testing and production. Its products cover work from gene sequencing and protein analysis to diagnostic tests and lab freezers, and its distribution arm ships supplies to labs worldwide. Drug developers also hire it to run clinical trials and to manufacture medicines under contract. It earns money from consumables that labs buy again and again, along with instrument sales, service contracts and outsourcing fees. The company traces its roots to Thermo Electron, founded in 1956, which merged with Fisher Scientific in 2006, and it is based in Waltham, Massachusetts.

Company size
10,001+
Company stage
IPO
Headquarters
Waltham, MA
Founded
1956

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