Teva Pharmaceuticals is a global leader in the pharmaceutical industry, dedicated to providing high-quality and affordable healthcare to millions of people worldwide. With a presence in nearly 60 countries and a diverse workforce, Teva’s mission is to make good health more accessible by producing generic medicines and essential drugs. As the world’s leading manufacturer of generic medicines, Teva has a strong commitment to helping people live healthier lives. At least 200 million people globally take a Teva medicine daily, and the company continues to innovate in improving global health.
Responsibilities in the Job
The Clinic Study Administrator at Teva Pharmaceuticals plays a crucial role in supporting, facilitating, and coordinating the daily activities of Bioavailability/Bioequivalence (BA/BE) studies. You will work under the direction of the Team Lead, Manager of Clinical Operations, and Clinical Principal Investigator (PI).
Your key responsibilities will include:
- Participating in subject enrollment for new BA/BE studies.
- Coordinating screening activities to ensure studies start on time, including counseling volunteers before their enrollment.
- Ensuring screening activities are carried out in compliance with Good Clinical Practice (GCP) and the approved study protocol.
- Communicating with volunteers about clinical trials, obtaining general consent, and ensuring study-specific tests are performed after obtaining additional consent.
- Maintaining a subject database, including updating adverse events (AEs), urine drug screening (UDS), and alcohol breath analysis (ABA) after study completion.
- Coordinating with the pathology laboratory for screening, post-study, and follow-up sample analysis.
- Ensuring consistency in screening activities and preparing study information.
- Participating in the informed consent process and ensuring the screening area is maintained clean and organized.
- Assisting in the check-in process and checking X-ray accountability before archival.
- Coordinating with the Head of Clinical Operations on all study-related activities and providing general support in the study.
Qualifications
To qualify for the role of Clinic Study Administrator, candidates must have:
- Education: Any Graduate and DMLT, BSc. Nursing.
- Experience: A minimum of 2 years of experience in volunteer recruitment, phlebotomy, or as a nurse in a reputed BA/BE center.
The role requires strong interpersonal and communication skills, as engaging with research subjects and explaining study protocols will be an integral part of the job.
Skills Required
The ideal candidate should possess the following skills:
- Excellent Communication Skills: Ability to explain complex clinical trial details and obtain informed consent from participants.
- Attention to Detail: Ensure accuracy in maintaining subject databases, documentation, and screening activities.
- Problem-Solving Abilities: Address volunteer concerns and ensure smooth execution of clinical trial processes.
- Team Collaboration: Work effectively with other clinical staff, researchers, and volunteers.
- GCP and Clinical Trial Knowledge: Understanding of Good Clinical Practice and experience in clinical research environments is highly beneficial.
- Adaptability and Flexibility: Ability to carry out diverse tasks and respond to management needs as they arise.
