PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Advertisement

Bioplus Life Sciences is Hiring for Medical Affairs (Clinical Development)

Published on

Bioplus Life Sciences has announced an exciting opportunity for early-career professionals in Medical Affairs. This role is ideal for candidates who want to work at the intersection of clinical development, regulatory strategy, and innovative NCE (New Chemical Entity) programs. Based in Whitefield, this position offers exposure to global regulatory submissions including USFDA, EMA, and DCGI.

If you are passionate about clinical research, drug development, and cross-functional collaboration, this role provides a strong platform to grow in the pharmaceutical and biotech industry.

Advertisement

Job Overview

  • Position Name: Assistant Manager / Deputy Manager โ€“ Medical Affairs (Clinical Development)
  • Company Name: Bioplus Life Sciences
  • Location: Whitefield, India
  • Experience: 1โ€“3 Years
  • Qualification: MD / PhD / PharmD

Roles and Responsibilities

As part of the Medical Affairs team, you will play a key role in supporting clinical development activities. Your responsibilities will include:

  • Contributing to clinical development plans aligned with regulatory strategies
  • Supporting clinical study design including protocols, synopses, and endpoints
  • Assisting in feasibility assessments and study execution planning
  • Reviewing clinical data and preparing documentation for regulatory submissions
  • Collaborating with cross-functional teams including R&D, regulatory, and clinical operations
  • Ensuring compliance with ICH-GCP guidelines and global clinical standards

Required Qualifications

Candidates applying for this role should meet the following criteria:

  • MD, PhD, or PharmD qualification in relevant field
  • 1โ€“3 years of experience in pharmaceutical or biotech industry
  • Hands-on exposure to clinical development, especially late-stage NCE programs
  • Understanding of ICH-GCP guidelines and clinical research processes
  • Strong analytical, communication, and documentation skills

Salary and Benefits

  • Estimated Salary Range: โ‚น6,00,000 โ€“ โ‚น12,00,000 per annum (based on experience and qualifications)
  • Opportunity to work on global regulatory submissions (USFDA, EMA, DCGI)
  • Exposure to advanced clinical development and translational research
  • Collaborative and growth-oriented work environment

How to Apply

Interested candidates can apply by sending their updated resume to:

๐Ÿ“ง talent.acquisition@bioplus.in
๐ŸŒ Visit: https://bioplus.in

Share This Job

โœ… Job Details Copied!