Teva Pharmaceutical Hiring Clinical Research Associate I (Bioanalytical)

Teva Pharmaceutical Hiring Clinical Research Associate I (Bioanalytical) in Seawoods, Navi Mumbai – M.Sc./M. Pharm Required

Teva Pharmaceutical, a global leader in generic medicines and committed to improving health worldwide, is seeking a Clinical Research Associate I (Bioanalytical) to join our team in Seawoods, Navi Mumbai. This role requires an M.Sc./M. Pharm degree and 2-4 years of relevant experience. Join us to contribute to groundbreaking pharmaceutical research and development.

About Teva Pharmaceutical

Teva Pharmaceutical is renowned for its dedication to enhancing health and providing access to high-quality health solutions. As the world’s largest producer of generic medicines, Teva is at the forefront of pharmaceutical innovation, making a significant impact on global health.

Job Details and Qualifications

Position: Clinical Research Associate I (Bioanalytical)

• Location: Seawoods, Navi Mumbai
• Experience:  At least 2-8 years of experience as a Clinical Research Coordinator in reputed BA/BE center.
• Qualification:  B. Pharm, M. Pharm or M.Sc. (Clinical Research).

Job Description: As a Clinical Research Associate I (Bioanalytical) at Teva Pharmaceutical, you will:

• Actively participate in method development, validation, and subject sample analysis.
• Process and analyze subject samples according to project requirements.
• Ensure availability of necessary resources, including chemicals, standards, biological matrices, and consumables before project commencement.
• Prepare detailed technical documents such as protocols, method SOPs, and procedural SOPs.
• Dispose of samples post-study as per procedural guidelines.

Key Responsibilities

• Overseeing the smooth running of BA/BE studies.
• Collecting, compiling, completing and reviewing data obtained from research.
• Informing participants about study during ICF process.
• Get involved in the Investigational product administration process.
• To act as a custodian and monitoring of research participants to ensure adherence to study rules.
• Adhering to research regulatory standards and in-house SOPs.
• Adhering to ethical standards like ICH-GCP and GLP.
• Maintaining detailed records of studies as per FDA and other required guidelines, including things such as drug administration and subject specific case report forms.
• Co-ordination with pathology laboratory regarding screening, post study and follow up sample analysis.
• Participating in subject enrollment efforts for new BA/BE studies.
• Ensuring that the necessary supplies and equipment for a study are available before initiation of study.
• Engaging with study staff for timely completion of study documentation to meet stringent timelines of project submission.
• Collects data as required by the protocol. Assures timely completion of Case Report Forms.
• Maintains study timelines.
• Completes study documentation and maintains study files in accordance with requirements as per in house SOPs and procedures including, but not limited to, consent forms, source documentation, case report forms and investigational material accountability forms (if required).
• Engaging with subjects and understanding their concerns.

Qualifications and Skills

• Educational Background: M.Sc./M. Pharm in a relevant field.
• Experience: 2-4 years in bioanalytical research.
• Technical Skills: Proficiency in method development and sample analysis.
• Documentation Skills: Ability to prepare detailed technical documents and SOPs.
• Resource Management: Efficient management of project resources and materials.

How to Apply

Interested candidates are invited to apply here. Apply online

Tagged as: Good Clinical Practice (GCP)