WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now

Clinical Research Job: Protocol Writer Opening at Synergen Bio – Apply Now!

Published on

Verified Job

Why Use Pharmabharat?

Real-Time Job Alerts

Trusted by Top Pharma Employers

Exclusive Pharma Industry Insights

Verified & Trusted Listings

Synergen Bio Private Limited is a DCGI (CDSCO)-approved Clinical Research Organization (CRO) offering end-to-end clinical research solutions for pharmaceutical and biotech industries. Established by a team of passionate professionals, Synergen Bio is committed to delivering high-quality, cost-effective clinical research services with expertise in regulatory compliance and project management.

With a focus on innovation, quality, and efficiency, Synergen Bio provides customized clinical trial solutions, including protocol development, clinical study reports, bioanalytical services, and regulatory submissions.

Job Opening: Protocol Writer

Department: Project Management & Biopharmaceutics

Qualification: B.Pharm / M.Pharm

Experience: 1 to 2.5+ years

Vacancies: 02

Job Location: Shivajinagar, Wakadewadi, Pune

Key Responsibilities:

  • Preparation of study synopsis and feasibility reports for clinical trials.
  • Drafting and reviewing clinical trial protocols as per sponsor and regulatory (DCGI, ICH-GCP) guidelines.
  • Developing Informed Consent Documents (ICD) in English and regional languages.
  • Compiling Clinical Study Reports (CSR) within timelines, ensuring regulatory compliance.
  • Coordinating with clinical, bioanalytical teams, and investigators for data compilation and interpretation.
  • Liaising with Ethics Committees (EC) for approvals and submissions.
  • Preparing Module 5 (Clinical Study Reports), Module 2.7, and bio-summary tables for regulatory filings.
  • Drafting confinement reports and annual summary reports.
  • Reviewing and updating Standard Operating Procedures (SOPs).

Preferred Candidate Profile:

  • B.Pharm / M.Pharm graduates with 1-2.5 years of experience in clinical research, protocol writing, or regulatory submissions.
  • Strong understanding of ICH-GCP, DCGI, and CDSCO guidelines.
  • Excellent scientific writing and documentation skills.
  • Ability to work in a fast-paced CRO environment.
  • Immediate joiners preferred.

How to Apply?

Interested candidates can share their updated CV at careers@synergenbio.com before June 20, 2025.

Note: Only shortlisted candidates will be contacted for further selection processes.

See also  Dr. Reddy’s Laboratories Hiring For Microbiologist Role