Associate Medical Director / Principal Investigator

Work Schedule

Other

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. 

Location/Division Information:

Location: Onsite Las Vegas, NV

​*Must be legally authorized to work in the United States without sponsorship.

*Must be able to pass a comprehensive background check, which includes a drug screening.

Due to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is an office-based position for a motivated Physician. The Associate Medical Director serves as the physician investigator on all assigned clinical trials providing medical oversight for a particular protocol and client. Ensures that the protocol is being conducted under all applicable laws, regulations and per ICH-GCP guidelines in the organization's Clinical Research Unit (CRU). Consults with clients and provides scientific and medical insight for protocols. Researches compounds being considered by the CRU for subject safety. Evaluates and signs off on medical data collected, completed case report forms (CRFs) and final clinical study reports (CSRs). Fosters relationships with clients and supports operational and business development staff. Supports local team in all quality initiatives and regulatory requirements at a busy Phase 18,000 sq feet, 32 bed facility understanding that participants often domiciled for extended duration.

Essential Functions:

• Reviews protocols for scientific, logistical and safety feasibility, as requested.
• Adheres to client directives and study protocols for assigned projects.
• Performs role as described in FDA Form 1572, including, but not limited to informed consent and screening examinations of subjects, clinical management of safety issues for the individual subjects as well as the study cohort.
• Presents all first-in-human and other high-risk trials to the Human Safety Committee (HSC) to ensure those trials are thoroughly reviewed and approved by the voting members. Develops a risk management plan (RMP) with the Project Manager to mitigate any risk to subject safety for all studies.
• Provides training on assigned studies, as requested.
• Discusses medical concerns with investigators and clients (e.g. discussion regarding interpretation of inclusion/exclusion criteria) raised during the course of a study, as appropriate, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study.
• Provides medical consultation to team members and answers study related medical questions. Communicates with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately. Deviates from current approved study protocol only if it is in the medical emergent safety needs of a study participant.
• Monitors, evaluates and takes action as needed on safety variables (adverse events, laboratory/ECG abnormalities, changes in patient medical status, and unblinding requests) during a clinical trial.
• Assesses reported adverse events and determines causality and study drug relationship. Assesses and determines the clinical significance of out-of-range laboratory values and other observed abnormalities noted within safety assessments.
• Contributes to departmental process improvement initiatives.
• Available for weekend call coverage (rotated through investigator team)

Education and experience:

• A valid medical degree (M.D. or D.O.)
• A medical license in good standing, with unrestricted ability to practice in place of work, where Applicable.  Nevada State licensure will be required.
• Board Certification in respective field preferred.
• A valid ICH GCP certificate (this can be acquired upon employment)
• No previous experience in clinical research is required but is preferred.
• Must have general medical practitioner diagnosis and treatment profic