Job Openings at Micro Data Labs (MDL)
Micro Data Labs (MDL) is seeking talented and motivated individuals to join our expanding team. We have multiple urgent openings across various departments, including Pharmacovigilance, Clinical Data Management (CDM), Clinical Research Coordination (CRC), Optometry, and Biostatistics. If you are a life sciences, pharmacy, clinical research, or biostatistics professional looking for a challenging and rewarding career with opportunities for growth, we encourage you to apply. Several positions offer work-from-home options. Immediate joiners are preferred.
Application Deadline: December 5th, 2025
Job Summary
Company: Micro Data Labs (MDL)
Location: Various (On-site and Work-From-Home)
Positions Available: 12
Departments: Pharmacovigilance, CDM, CRC, Optometry, Biostatistics
Experience Levels: Entry-Level to Experienced
Job Type: Full-time
Responsibilities
The specific responsibilities will vary depending on the position. Below is an overview of the key duties for each role:
Pharmacovigilance Associate (2 Positions – WFH):
- Writing and maintaining safety documents, including PSURs, RMPs, and PSMFs.
- Ensuring compliance with pharmacovigilance regulations and guidelines.
Optometrist (2 Positions – On-site):
- Conducting ophthalmic examinations and diagnostics.
- Providing patient care and managing eye conditions.
- Contributing to clinical research studies related to vision and eye health.
CDM Executive (2 Positions – WFH):
- Managing clinical data using Electronic Data Capture (EDC) systems.
- Designing Case Report Forms (CRFs) and implementing data validation procedures.
- Ensuring data quality and integrity throughout clinical trials.
Clinical Research Coordinator (CRC) (4 Positions – Punjab & Delhi):
- Coordinating clinical trial activities at research sites.
- Recruiting and screening potential study participants.
- Collecting and managing data according to study protocols.
- Ensuring compliance with ethical guidelines and regulatory requirements.
Bio-Statistician (2 Positions – WFH):
- Performing statistical analysis of clinical trial data.
- Developing statistical analysis plans and reports.
- Contributing to the design and interpretation of clinical studies.
Requirements
Pharmacovigilance Associate:
- Minimum 1 year of experience in pharmacovigilance.
- Strong understanding of PV regulations & compliance.
- Proficiency in writing PSUR, RMP, PSMF.
- Bachelor’s or Master’s degree in a relevant field (e.g., Pharmacy, Life Sciences).
Optometrist:
- Relevant degree in Optometry.
- Research experience preferred.
- Clinical research exposure is a plus.
- Excellent patient handling and ophthalmic diagnostic skills.
CDM Executive:
- Minimum 1 year of experience in Clinical Data Management.
- Experience with EDC systems (e.g., Medidata Rave, Oracle Clinical).
- Proficiency in CRF design and data validation techniques.
- Bachelor’s degree in a related field.
Clinical Research Coordinator (CRC):
- Minimum 3 months of experience in clinical research coordination.
- Experience in site coordination and patient recruitment.
- Strong data collection and protocol compliance skills.
- Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing).
Bio-Statistician:
- Fresher to 1 year of experience.
- Knowledge of statistical analysis principles and methods.
- Familiarity with statistical software such as SAS or R (preferred).
- Bachelor’s or Master’s degree in Statistics or a related field.
Benefits
- Work-from-home options for select positions.
- Opportunity to work on global clinical research projects.
- Career growth and development in Pharmacovigilance, CDM, and Biostatistics.
- Supportive and research-driven work environment.
- Collaboration with multi-disciplinary healthcare teams.
How to Apply
Interested candidates are encouraged to apply immediately. Please send your resume to [email protected].
Important: Please use the following format for the email subject line:
Position Name ; Years of Exp ; Your Location
Example:
CDM ; 1yr Exp ; Chandigarh
Note: Applications that do not follow the specified subject line format may not be considered.