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.

Application Link

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.

AD