Bioclinaarc has announced a new hiring opportunity for life science professionals in key domains including Data Management, Pharmacovigilance/Drug Safety, Regulatory Affairs, and Biostatistics/SAS Programming.
This recruitment drive is an excellent opportunity for B.Pharm, M.Pharm, MSc, Biostatistics, and Life Science graduates who are looking to build a career in clinical research, drug safety, regulatory affairs, and clinical data analytics.
Candidates with experience in clinical data management, adverse event reporting, regulatory documentation, and SAS programming are encouraged to apply for these positions.
The company is currently hiring for the following roles.
Available Positions
| Position | Vacancies |
|---|---|
| Data Manager | 1 |
| Pharmacovigilance / Drug Safety Associate | 1 |
| Regulatory Affairs Associate | 2 |
| Biostatistician / SAS Programmer | 2 |
Key Responsibilities
Data Manager
- Manage and maintain clinical trial datasets and databases
- Perform data validation, query management, and data cleaning
- Ensure compliance with ICH-GCP, CDISC standards, and regulatory guidelines
- Coordinate with clinical research teams and biostatistics teams
Pharmacovigilance / Drug Safety Associate
- Process adverse event (AE) and serious adverse event (SAE) reports
- Perform MedDRA coding and case narrative preparation
- Conduct case triage, literature screening, and signal detection
- Maintain compliance with global pharmacovigilance regulations
Regulatory Affairs Associate
- Prepare and review regulatory submissions and dossiers
- Maintain regulatory documentation and compliance records
- Support regulatory strategy and product lifecycle management
- Coordinate with regulatory agencies and internal teams
Biostatistician / SAS Programmer
- Perform statistical analysis for clinical trials
- Develop SAS programs for clinical data analysis
- Prepare tables, listings, and figures (TLFs)
- Support study design and statistical modeling
Eligibility Criteria
Candidates applying for Bioclinaarc jobs in Pharmacovigilance, Data Management, Regulatory Affairs, and Biostatistics should meet the following qualifications:
Educational Qualification
- B.Pharm / M.Pharm
- MSc Life Sciences / Biotechnology / Biostatistics
- Statistics or Data Science background for SAS roles
Preferred Skills
- Knowledge of ICH-GCP guidelines
- Experience with clinical trial documentation
- Understanding of pharmacovigilance and regulatory frameworks
- Proficiency in SAS programming and statistical analysis
- Strong data management and analytical skills
Salary & Benefits
Bioclinaarc offers competitive salaries and career growth opportunities in the clinical research and pharmacovigilance industry.
Estimated Salary Range
- Data Manager: โน5 โ โน9 LPA
- Pharmacovigilance Associate: โน4 โ โน8 LPA
- Regulatory Affairs Associate: โน4 โ โน9 LPA
- Biostatistician / SAS Programmer: โน6 โ โน12 LPA
Benefits
- Exposure to global clinical research projects
- Career growth in pharmacovigilance and regulatory affairs
- Training on advanced data analytics tools
- Collaborative and research-driven work environment