Clinical Research Physician - Full-Time Onsite(Day Hours)

Thermo Fisher Scientific - Dallas, TX

Full-time - Mid Level

Dallas, TX

Computer and Electronic Product Manufacturing

About the position

The Clinical Research Physician at Thermo Fisher Scientific plays a crucial role in conducting clinical trials in accordance with ICH GCP, local regulations, and company processes. This position is responsible for ensuring the medical wellbeing and safety of study participants while driving the quality and oversight of clinical studies. The role involves managing multiple studies, engaging in recruitment initiatives, and ensuring compliance with ethical standards throughout the trial process.

Responsibilities

• Conduct clinical evaluations and assessments of participants to ensure eligibility and safety.
• Attend Site Initiation Visits (SIV), Pre-Selections Visits (PSV), and Investigator meetings as required.
• Participate in recruitment initiatives and strategy development to achieve enrollment targets.
• Review enrollment progress, pre-screening and screening success rates, and retention of participants.
• Interpret study protocols and Investigator's Brochure (IB).
• Manage and review Interactive Voice Response System (IVRS) and Case Report Forms (CRF)/Electronic Data Capture (EDC) as applicable.
• Oversee management of investigational medical products (IMP).
• Simultaneously manage multiple studies with higher participant numbers.
• Complete documentation for Principal Investigator (PI) handover.
• Ensure ethical conduct and safety of participants throughout the study.

Requirements

• A valid medical degree with at least 2 years of experience as a licensed physician.
• Valid registration as a medical practitioner with an unrestricted ability to practice.
• Exceptional proficiency in general medical diagnosis and treatment.
• At least one year of experience in clinical research or comparable expertise in clinical trials.
• A valid ICH GCP certificate (can be obtained after employment).
• Thorough understanding of medical terminology, drug safety, and lab report interpretation.
• Working knowledge of scientific concepts related to clinical trial design and analysis.
• Strong critical thinking, decision-making, analytical, and problem-solving skills.
• Exceptional communication skills and ability to work collaboratively with cross-functional teams.
• Excellent written, verbal, and presentation skills.
• Ability to manage multiple projects effectively and prioritize tasks under pressure.

Nice-to-haves

• Experience with project management tools and methodologies.
• Familiarity with regulatory requirements in clinical research.

Benefits

• Career development resources and opportunities.
• Access to a global network of clinical research professionals.
• Supportive work environment focused on health and safety.