Jeevan Scientific Technology Limited (JSTL) is a leading Contract Research Organization (CRO) based in Hyderabad, India. The company specializes in clinical research, pharmacovigilance, bioavailability/bioequivalence (BA/BE) studies, and regulatory consulting services. With a commitment to innovation and excellence, JSTL provides high-quality services to the pharmaceutical and healthcare industries.
Available Job Openings
1. Drug Safety Associate / Senior Associate – Medical Information Call Center (Pharmacovigilance)
Location: Hyderabad
Experience: 0 – 3 years
Qualification: B.Pharm/M.Pharm/Pharm D/BDS
Responsibilities:
- Handling medical information queries through the call center.
- Managing pharmacovigilance cases as per regulatory requirements.
- Documenting and reporting adverse drug reactions (ADR).
2. Clinical Research Associate – Clinical Trials
Location: Hyderabad
Experience: 2-5 years
Qualification: M.Pharm (Pharmacology)
Responsibilities:
- Supporting clinical trial operations for biosimilars and small molecules.
- Monitoring and ensuring compliance with Good Clinical Practices (GCP).
- Conducting site visits and overseeing trial execution. Note: Female candidates are preferred.
3. Manager – Pharmacovigilance Department
Location: Hyderabad
Experience: 7 – 10 years
Qualification: MBBS/MD/M.Pharm
Responsibilities:
- Leading pharmacovigilance teams and ensuring compliance with global regulations.
- Overseeing case processing, signal detection, and risk management.
4. Team Leader – Pharmacovigilance
Location: Hyderabad
Experience: 5 to 7 years
Responsibilities:
- Managing a team of Drug Safety Associates.
- Ensuring timely submission of safety reports.
- Coordination with regulatory authorities.
5. Clinical Trials Project Management – Executive
Location: Hyderabad
Experience: 3-5 years
Qualification: M.Sc. (Life Sciences), MS Pharmacy, PharmD, PhD, MD preferred
Responsibilities:
- Managing project timelines and deliverables for clinical trials.
- Coordinating between sponsors and cross-functional teams.
6. Clinical QA Auditor
Location: Hyderabad
Experience: 2-5 years
Qualification: B.Sc/M.Sc/B.Pharm/M.Pharm
Responsibilities:
- Conducting GCP quality assurance audits.
- Ensuring adherence to ICH-GCP, US, and EU regulations.
7. Medical Monitor – Clinical Trials & Pharmacovigilance
Location: Hyderabad
Experience: Freshers
Qualification: MBBS, MD-Pharmacology
Responsibilities:
- Providing medical oversight for clinical trials.
- Assessing safety data and adverse event reports.
8. Clinical Trial Assistant
Location: Hyderabad
Experience: 2-3 years
Qualification: Any Bachelor’s Degree in Life Sciences
Responsibilities:
- Supporting clinical trial teams with documentation and coordination.
- Ensuring compliance with study protocols.
9. Drug Safety Physician – Pharmacovigilance
Location: Hyderabad
Experience: 1-4 years
Qualification: MBBS/MD
Responsibilities:
- Reviewing and analyzing individual case safety reports (ICSRs).
- Ensuring compliance with pharmacovigilance regulations.
10. Project Manager – Clinical Trials
Location: Hyderabad
Experience: M.Pharm (1-2 years), B.Pharm (2-4 years)
Responsibilities:
- Managing project deliverables in biosimilars and small molecule trials. Note: Female candidates are preferred.
11. BA/BE Project Coordinator
Location: Hyderabad
Experience: 0-2 years
Qualification: M.Pharm/MBA
Responsibilities:
- Coordinating bioavailability/bioequivalence (BA/BE) studies.
- Assisting in project planning and execution.
Required Skills
- Strong understanding of clinical research and pharmacovigilance regulations.
- Good communication and teamwork skills.
- Proficiency in medical documentation and reporting.
- Experience with GCP, ICH, and regulatory guidelines.
- Ability to manage multiple projects and deadlines.
Interested candidates can apply by sending their updated resumes to Hr@jeevanscientific.com. For specific job roles, please mention the position in the subject line.
