"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs"

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"Syneos Health Hiring Safety & PV Coordinator in Hyderabad | Pharmacovigilance Jobs" (Syneos Health Hiring Safety & PV Coordinator in Hyderabad) Introduction Candidates looking to build a strong and long-term career in Pharmacovigilance (PV) and Drug Safety have an excellent opportunity at Syneos Health , a globally recognized biopharmaceutical solutions organization. Syneos Health is currently hiring for the position of Safety & PV Coordinator at its Hyderabad office . This is a full-time, office-based role , ideal for professionals who have experience or exposure in pharmacovigilance submissions, safety reporting, regulatory compliance, and clinical research processes . Working with a global organization like Syneos Health provides exposure to international safety regulations, cross-functional teams, and structured career growth . About The Company – Syneos Health Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports pha...

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"Medical Writing Jobs 2025 | Samahitha Hiring Life Science Graduates (Immediate Joiners)"

"Samahitha Hiring Life Science Graduates for Junior Medical Writer Role – Apply Now"

(Medical Writing Jobs 2025)

Samahitha, a reputed organization in the clinical research and healthcare industry, is inviting applications for the position of Junior Medical Writer. This is an excellent opportunity for Life Science graduates with 1–2 years of medical writing experience who are looking to advance their careers in a dynamic and growth-oriented environment.

The role involves working on regulatory documents, clinical trial protocols, and scientific writing that contribute to international healthcare and pharmaceutical projects. Immediate joiners are preferred.


Job Responsibilities:-

As a Junior Medical Writer at Samahitha, your key responsibilities will include:

  • Drafting and reviewing clinical trial protocols, investigator brochures, informed consent forms, and regulatory submissions.
  • Preparing safety narratives, clinical study reports, and scientific manuscripts.
  • Ensuring scientific accuracy, ethical compliance, and adherence to regulatory standards.
  • Collaborating with clinical operations, regulatory affairs, and data management teams.
  • Conducting literature reviews, medical summaries, and risk assessments.
  • Assisting in protocol-related clarifications and medical queries.
  • Staying updated with ICH-GCP guidelines and industry regulations.

Qualifications Required:-

Candidates applying for this role should have:

  • Education: Bachelor’s or Master’s degree in Life Sciences (Pharma, Biotechnology, Biochemistry, etc.).
  • Experience: 1–2 years of experience in medical writing or clinical documentation.
  • Strong communication and writing skills.
  • Knowledge of ICH-GCP guidelines, clinical research processes, and regulatory documentation.
  • Ability to deliver error-free documents within timelines.
  • Must be an immediate joiner.

Benefits of Joining Samahitha:-

  • Opportunity to work on global clinical research projects.
  • Career growth in scientific and regulatory writing.
  • Collaborative and supportive work environment.
  • Competitive annual salary package (INR 3,00,000 – 5,00,000).

How to Apply:-

If you meet the eligibility criteria, send your updated CV to:
📧 career@samahitha.com

Take the next step in your career with Samahitha and contribute to impactful medical writing projects in the healthcare industry.

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