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Navitas Life Sciences Hiring Freshers & Experienced in regulatory affairs, pharmacovigilance, clinical research, and CDM & SAS

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Are you a life sciences professional looking to advance your career in the pharmaceutical and clinical research industry? Navitas Life Sciences, a leading global partner for life sciences organizations, is hiring for 5 key roles across Chennai and Bangalore. If you have a passion for regulatory affairs, pharmacovigilance, or clinical data analysis, this is your chance to join a dynamic team and contribute to groundbreaking projects.

Read on to learn more about the job openings, company details, and how to apply.


About Navitas Life Sciences

Navitas Life Sciences is a trusted partner for pharmaceutical, biotech, and medical device companies worldwide. With a focus on innovation and quality, Navitas provides end-to-end solutions in regulatory affairspharmacovigilanceclinical research, and data sciences. The company is committed to delivering excellence while fostering a collaborative and inclusive work environment.

Navitas Life Sciences is known for its expertise in navigating complex regulatory landscapes, ensuring compliance with global standards, and driving successful outcomes for its clients.


Job Openings at Navitas Life Sciences

1. Junior Regulatory Associate

Location: Chennai, India
Job Type: Full Time
Experience Level: Junior
Qualifications: Bachelor’s Degree in Pharma

Key Responsibilities:

  • Understand regulatory submission requirements for IND, ANDA, NDA, and DMF in CTD/eCTD formats for agencies like US-FDA, EMA, and Health Canada.
  • Assist in document-level publishing, including bookmarking, hyperlinking, and preparing Tables of Contents.
  • Provide submission publishing support and ensure compliance with customer and organizational SOPs.

Desired Skills:

  • Experience in publishing and submissions.
  • Strong attention to detail and organizational skills.

2. Regulatory Associate – Trainee

Location: Chennai, India
Job Type: Full Time
Experience Level: Junior
Qualifications: Bachelor’s Degree in Pharma

Key Responsibilities:

  • Support regulatory submissions in CTD/eCTD formats for global regulatory agencies.
  • Assist in document-level publishing and submission archiving.
  • Ensure adherence to customer and organizational policies.

Desired Skills:

  • Experience in publishing and submissions.
  • Knowledge of regulatory guidelines and processes.

3. Safety Specialist II

Location: Bangalore, India
Job Type: Full Time
Experience Level: Analyst
Qualifications: Graduate/Post Graduate in Life Sciences, Pharmacy, Medicine, or related fields.

Key Responsibilities:

  • Author and review aggregate safety reports (DSURs, PBRERs, PSURs, etc.).
  • Perform signal management and risk management plan activities.
  • Ensure compliance with pharmacovigilance guidelines (GVP, ICH, USFDA).

Desired Skills:

  • Strong understanding of pharmacovigilance and regulatory guidelines.
  • Proficiency in MS Office and excellent communication skills.

4. Principal SAS Programmer

Location: Bangalore, India
Job Type: Full Time
Experience Level: Manager
Qualifications: Graduate/Post Graduate in Life Sciences

Key Responsibilities:

  • Lead programming deliverables for high-complexity projects.
  • Create and validate safety and efficacy analysis datasets (CDISC standards).
  • Manage timelines, troubleshoot programming issues, and foster client relationships.

Desired Skills:

  • Expertise in SAS programming and SDTM/ADaM datasets.
  • Strong problem-solving and people management skills.

5. Clinical Data Analyst

Location: Chennai and Bangalore, India
Job Type: Full Time
Experience Level: Junior
Qualifications: Life Sciences or Engineering Graduate

Key Responsibilities:

  • Create efficacy and safety tables, listings, and figures.
  • Develop and validate SAS macros.
  • Manage multiple projects and meet deadlines independently.

Desired Skills:

  • 2.5–3 years of experience in clinical data analysis.
  • SAS certification and in-depth knowledge of clinical development processes.

Why Join Navitas Life Sciences?

  • Global Exposure: Work on projects for leading regulatory agencies like US-FDA, EMA, and Health Canada.
  • Career Growth: Opportunities to learn and grow in a fast-paced, innovative environment.
  • Work-Life Balance: Flexible work policies and a supportive team culture.
  • Impactful Work: Contribute to life-changing therapies and medical advancements.

How to Apply

If you’re ready to take the next step in your career, we’d love to hear from you! To apply for any of the above positions

Send Your Resume According To Location You want to Apply ->

recruitment.india@navitaslifesciences.com

recruitment.bangalore@navitaslifesciences.com

recruitment.chennai@navitaslifesciences.com

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