Clinical Research Physician Investigator - Part Time

Thermo Fisher Scientific•San Antonio, TX

1d•Onsite

About The Position

The Clinical Research Physician Investigator conducts clinical trials in accordance with ICH GCP, local regulations, study protocols, and company processes. The role safeguards participant medical wellbeing and safety, provides clinical oversight and quality assurance for studies at the site and, with PI oversight, at other sites, and collaborates with sponsors, clients, and site staff. The investigator contributes to study delivery and site commercial success through participant recruitment, enrollment, and retention. The role may serve as PI and sub-investigator across multiple studies, contribute to site processes and best practices, and support the development of junior physicians through training, mentoring, and general assistance. This is a part-time, onsite position in San Antonio, expected to total 22 hours per week. The preferred schedule is Monday through Friday, 8:30 a.m. to 1:00 p.m. CST, with some flexibility potentially required. Relocation assistance is not provided. The employee must be legally authorized to work in the United States without sponsorship and pass a comprehensive background check, including drug screening.

Requirements

Valid medical degree in the country of practice and at least 3 years of experience working as a licensed physician.
Valid medical practitioner registration and a medical license in good standing, with unrestricted ability to practice at the place of work where applicable.
Other medical licenses required in the country of practice, such as a dispensing license, where applicable.
Sufficient clinical expertise and medical judgment to safely conduct protocol-driven clinical research and oversee study participants.
Exceptional proficiency in general medical practitioner diagnosis and treatment.
Exceptional understanding of medical terminology, drug safety, and interpretation of laboratory reports.
Thorough understanding of scientific concepts related to clinical trial design and analysis.
Excellent written, verbal, and presentation skills.
Ability to work well under pressure and effectively prioritize and manage multiple projects.
Strong planning, organizational, and project management skills.
Ability to manage outside agencies to fulfill project objectives.
Self-starter able to thrive under pressure in a fast-paced environment.
Proficiency with Word, Excel, and PowerPoint, and the Internet.
Ability to demonstrate strategic leadership by influencing the site team to deliver on targets.
Legal authorization to work in the United States without sponsorship.
Ability to pass a comprehensive background check, including drug screening.
Ability to meet the stated physical and work-environment requirements, including frequent stationary work, mobility, repetitive hand movements, occasional bending and lifting, computer use, communication, multitasking, and working under stress.

Nice To Haves

Prior clinical research experience is preferred but not required.
A valid ICH GCP certificate; it can be obtained after employment.
Strong clinical backgrounds seeking to transition into clinical research are encouraged to apply.

Responsibilities

Conduct clinical evaluations and assessments to determine participant eligibility and monitor safety and adherence.
Attend Site Initiation Visits, Pre-Selection Visits, and investigator meetings as required.
Participate in recruitment initiatives and strategy development to achieve enrollment targets within planned timelines.
Review enrollment progress, pre-screening and screening success rates, screen failure rates, participant safety, and retention.
Interpret study protocols and Investigator's Brochures.
Manage and review IVRS and CRF/EDC systems, if applicable.
Oversee management of investigational medical products (IMP).
Identify and report study trends relevant to study conduct and outcomes.
Oversee multiple studies and/or studies with higher participant numbers.
Prioritize participant safety and protection through ethical conduct throughout all aspects of each study.
Fulfill medical duties and ensure clinical trials meet acceptable medical, scientific, and ethical standards and comply with protocols, SOP/COP, ICH, and local GCP guidelines and regulations.
Provide clinical oversight and ensure study quality at the site, or at other sites with PI oversight.
Contribute to site study targets, including recruitment, enrollment, and participant retention.
Support junior physicians through training, mentoring, and general support.
Provide input into site processes and share best practices.
Collaborate effectively with sponsors, clients, and site staff.