PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose- to improve health!

Accelerated Enrollment Solutions (AES) is a business unit of PPD that helps biopharmaceutical companies overcome patient recruitment and research site challenges by optimizing each step in the patient journey to deliver greater speed, certainty, and control to clinical trial delivery.

As a Research Physician you will be a key member impacting the development and research for therapeutics for patients.

At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. We offer continued career advancement opportunities, award winning training and benefits focused on the health and well being of our employees.

Summarized Purpose:

Conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes. Ensures the medical wellbeing and safety of the participants through the safe performance and execution of the studies. Maintains clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site which includes recruitment, enrollment, and retention of study participants.

Essential Functions:

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  Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies.

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  Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants.

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  Interprets protocols and IB and participate in initiatives to strategize for patient recruitment.

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  Ensures and protect the welfare and safety of participants through ethical conduct; this should receive the highest priority at all times during all aspects of the study.

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  Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.

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  Reports any safety threats, that may impact stakeholders/participants and action complaints or QIs as per site processes.

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  Exercises meticulous attention to detail in recording information and source management.

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  Actively involved in audit preparations and site inspections.

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  Oversees the management of investigational medical product (IMP).

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