Clinical Research Physician (General Medicine)

retention of study participants.

Practice Info
• Trialmed helps biopharmaceutical companies overcome patient enrollment and research site challenges by combining a powerful patient recruiting solution with more than 150 clinical research sites located throughout the world.
• As a business of PPD, we are committed to optimizing each step in the patient journey and delivering best-in-class site performance to bring our customers greater certainty to clinical trial delivery.

Responsibilities
• Conduct all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes.
• Ensure the medical wellbeing and safety of the participants through the safe performance and execution of the studies.
• Maintain clinical oversight and quality on the studies registered on and deliver on study targets, thereby contributing to the commercial success of the site which includes: recruitment, enrolment and retention of study participants.
• Carry out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies.
• Review enrollment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants.
• Interpret protocols and IB and participate in initiatives to strategize for patient recruitment.
• Fulfill and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
• Report any safety threats that may impact stakeholders/participants and action complaints or QIs as per site processes.

Shift & Schedule
• Standard (Mon-Fri)
• Gen Med Hours: 4 days/week with approx. 3 hours/day. Some flexibility around days/hours might be able to be accommodated.

Requirements
• 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.
• A valid medical degree and registration within the country of practice.
• A medical license in good standing, with unrestricted ability to practice in place of work, where applicable.
• A valid ICH GCP certificate (can be obtained after employment).
• Exceptional general medical practitioner diagnosis and treatment proficiency.
• At least one-year experience working in clinical research, or comparable research/clinical expertise to demonstrate the ability to work in clinical trials.