Looking for a new job opportunity in the life sciences industry? Whether you are an aspiring Clinical Data Analyst, MICC Associate, Regulatory Associate, or Bioanalytical Scientist, we’ve got you covered. This article breaks down each role, highlighting responsibilities, required skills, and how to apply for these exciting roles.

Clinical Data Analyst – Chennai & Bangalore, India

Company Introduction:
We are a leading organization in clinical research, offering dynamic work opportunities to data experts. We are currently seeking a Clinical Data Analyst with strong SAS programming skills.

Responsibilities in Job

• Create efficacy and safety tables, listings, and derived datasets.
• Develop and validate SAS macros for projects.
• Simultaneously manage multiple projects to meet deadlines.
• Lead a team independently with minimal guidance from biostatisticians.

Qualifications and Skills

• 2.5 – 3 years of experience in clinical data analytics.
• Strong knowledge of clinical development and regulatory processes.
• SAS certification is highly preferred.
• Ability to work independently and collaborate with teams.

Junior MICC Associate – Pharmacovigilance Support (Bangalore, India)

Join our growing Medical Information Contact Centre (MICC, a part of our pharmacovigilance operations, ensuring product safety and compliance with global regulations.

Responsibilities in Job

• Handle inquiries via phone, email, and follow-up responses.
• Perform duplicate checks and case registration.
• Process individual case safety reports (ICSR) into safety databases.
• Coordinate audits and close CAPAs on time.
• Ensure compliance with global and local data privacy regulations.

Qualifications and Skills

• 1-3 years of MICC experience in a similar role.
• Graduate or postgraduate degree in life sciences.
• Strong communication and interpersonal skills.
• Familiarity with pharmacovigilance databases like MedDRA and WHO-DD.

Junior Regulatory Associate – Publishing and Submissions (Chennai)

We are an established leader in regulatory affairs, looking for a Junior Regulatory Associate to assist in publishing and submission processes.

Responsibilities in Job

• Assist with regulatory submissions such as IND, NDA, ANDA, and DMF in CTD/eCTD formats.
• Support the publishing and bookmarking of regulatory documents.
• Archive and review submissions and ensure they meet timelines.
• Maintain compliance with both customer SOPs and company policies.

Qualifications and Skills

• 0 – 1 Year
• Familiarity with US-FDA, EMA, and other global regulatory bodies.
• Strong attention to detail and organizational skills.

Bioanalytical Scientist – Manipal, India

Responsibilities in Job

• Develop and validate bioanalytical methods using LCMS, HPLC, and GCMS instruments.
• Maintain calibration of sophisticated instruments.
• Ensure compliance with USFDA guidelines for bioanalytics.
• Improve team productivity and Turn Around Time (TAT).

Qualifications and Skills

• 2 – 5 years of experience in bioanalytical roles.
• Bachelor’s degree in Pharma or relevant field.
• Strong expertise in LC-MS and HPLC operations.
• Excellent communication and team coordination skills.

How To Apply

mailto: recruitment.chennai@navitaslifesciences.com With Proper Subject Line For Which Position You are Applying