Precision Medicine Group has announced multiple job opportunities in India for professionals seeking careers in clinical research, quality assurance, clinical data management, clinical systems, healthcare data governance, and competitive intelligence.
The latest Precision Medicine Group hiring 2026 includes five positions based in Bangalore and Remote India. Opportunities range from Clinical Data Associate and Data Steward positions to senior Clinical Systems and Quality Assurance roles.
Candidates with qualifications in Pharmacy, Life Sciences, Biology, Chemistry, Healthcare, Computer Science, Information Management, Business, Marketing, Communications, and related disciplines may be eligible depending on the position.
Current Openings
| Position | Location | Key Experience |
|---|---|---|
| Quality Assurance Specialist III | Bangalore | 4+ years |
| Senior Clinical Systems Administrator | Bangalore | 5+ years |
| Content Analyst (Data Steward) | Remote, India | 1โ3 years |
| Clinical Data Associate II | Bangalore | 2โ4 years |
| Analyst, Business & Competitive Intelligence | Remote, India | 6+ months relevant sales lifecycle experience |
1. Quality Assurance Specialist III
Location: Bangalore, Karnataka, India
The Quality Assurance Specialist III provides independent quality oversight for GLP and GCLP studies. The position focuses on study audits, computerized system audits, data integrity, regulatory compliance and verification of clinical and laboratory records.
Key Responsibilities
- Develop study-specific audit schedules and audit plans.
- Execute scheduled study audits and prepare audit reports.
- Review SOP alignment, document versions and study governing documents.
- Review clinical protocols, SAP/SAR documents and amendments.
- Review experiment records and batch records.
- Verify staff training and equipment/reagent qualification status.
- Review data tables, listings and summaries against Data Transfer Agreements.
- Ensure traceability between raw source data and reported outputs.
- Apply ALCOA+ data integrity principles during electronic data review.
- Review audit trails, metadata, system access and validation controls.
- Evaluate compliance with 21 CFR Part 11 and EU Annex 11.
- Identify data integrity gaps and risks affecting data reliability.
- Support regulatory, customer and notified-body audits.
- Assist with Quality personnel training.
Qualification & Experience
Candidates should have a Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biology, Chemistry or a related discipline.
A minimum of 4 years of relevant experience in a life sciences GxP environment is required, with CRO experience preferred.
Candidates should have working knowledge of:
- ICH-GCP E6 R2/R3
- 21 CFR Part 11
- EMA/EU CTR
- EU Annex 11
- GCP, GMP, GLP and GCLP
- ALCOA+ principles
- LIMS and computerized systems
- Computer System Validation (CSV)
- Computer Software Assurance (CSA)
- Data governance and audit trails
Certifications such as ASQ CQA, ISO 9001/13485 Lead Auditor, GxP Lead Auditor or Clinical QA certifications are advantageous.
2. Senior Clinical Systems Administrator
Location: Bangalore, Karnataka, India
The Senior Clinical Systems Administrator acts as a subject matter expert for clinical technology platforms and works with Clinical Systems management, Clinical Operations and IT teams to support system configuration, integration, testing, validation and adoption.
Key Responsibilities
- Maintain and update templates within clinical systems.
- Manage help-desk ticket assignments.
- Develop Clinical System processes and procedures.
- Oversee Clinical System and EDC integrations.
- Perform system archival activities.
- Serve as a Clinical Systems SME.
- Support end-user requests and troubleshooting.
- Configure templates, dashboards, reports and milestones.
- Support new system releases and configuration changes.
- Participate in system testing and validation.
- Execute User Acceptance Testing (UAT), when required.
- Manage ongoing end-user reviews.
- Support CTMS-related processes and training.
- Assist with inspection and audit readiness.
- Support CAPA development and execution where applicable.
Qualification & Experience
Candidates should possess a degree or equivalent experience, preferably within a business, scientific or healthcare discipline.
The role requires approximately 5 years of Clinical Systems experience.
Strong experience with clinical trial technology platforms is expected, including:
- CTMS
- EDC
- eTMF
- RTMS
- System configuration
- Requirements gathering
- System documentation
- Clinical system integrations
- Testing and validation
- UAT
Previous Clinical Operations experience involving clinical systems is preferred.
3. Content Analyst (Data Steward)
Location: Remote, India
The Content Analyst (Data Steward) is responsible for maintaining data accuracy, consistency, completeness and governance across Precision Medicine Group products.
This remote data stewardship position is particularly relevant for candidates with experience in data quality, metadata management, data lineage, healthcare data and data governance.
Key Responsibilities
- Validate, cleanse and enrich business and healthcare data.
- Monitor overall data quality.
- Identify critical data elements with stakeholders.
- Define and maintain data quality standards.
- Develop data dictionaries.
- Maintain metadata and data lineage documentation.
- Develop data governance policies and standards.
- Monitor data integrity across applications and systems.
- Conduct data profiling and quality analysis.
- Identify data quality issues and recommend corrective solutions.
- Maintain dashboards, scorecards and data quality reports.
- Integrate data management practices into operational workflows.
- Train end users on data management best practices.
- Support data privacy, security and regulatory compliance.
- Participate in enterprise data governance activities.
- Gather user/client feedback for data product improvements.
Qualification & Experience
Candidates should have a Bachelor’s degree in Computer Science, Information Management or a related field.
Applicants should generally have 1โ3 years of experience in data management, data governance or a related area, including approximately 1โ2 years of exposure to US healthcare data.
Relevant skills include:
- SQL
- Data governance
- Data quality
- Data lineage
- Metadata management
- Data profiling
- Database management
- Data modeling
- Data privacy and security
Experience with Reltio, Informatica or other Master Data Management (MDM) platforms is preferred. Familiarity with Snowflake is also advantageous.
4. Clinical Data Associate II
Location: Bangalore, Karnataka, India
The Clinical Data Associate II supports clinical trial data management activities throughout the study lifecycle, from study startup and database development through database lock and post-lock activities.
Key Responsibilities
- Support Lead Data Managers and project teams.
- Perform clinical data entry and quality control where required.
- Develop CRF specifications from clinical study protocols.
- Assist with clinical database development.
- Conduct database-build UAT.
- Maintain database-build documentation.
- Support development of electronic and manual edit checks.
- Create and maintain data management documentation.
- Train study personnel on CRFs, EDC systems and project requirements.
- Review clinical trial data according to the Data Management Plan.
- Generate and resolve clinical data queries.
- Perform line-listing data review.
- Generate patient- and study-level metrics.
- Support medical coding activities.
- Assist with SAE/AE reconciliation.
- Coordinate with EDC and external-data vendors.
- Support SAS programming and QC activities where required.
- Assist with troubleshooting operational data-management issues.
- Review protocols, SAPs and Clinical Study Reports where required.
- Support development and maintenance of Data Management SOPs.
- Communicate with sponsors, vendors and cross-functional study teams.
Qualification & Experience
Applicants should possess a Bachelor’s degree and/or an appropriate combination of education and related experience.
The position requires approximately 2โ4 years of relevant experience.
Experience in a clinical, scientific or healthcare discipline is preferred.
Knowledge or experience involving the following can strengthen a candidate’s profile:
- Clinical Data Management
- EDC
- CRF development
- Database UAT
- Clinical data review
- Query management
- SAE/AE reconciliation
- Medical coding
- Clinical databases
- SAS
- Microsoft Excel
5. Analyst, Business & Competitive Intelligence
Location: Remote, India
The Analyst, Business & Competitive Intelligence supports business development by researching pharmaceutical, biotechnology, CRO and specialty laboratory markets and identifying potential sales opportunities.
Key Responsibilities
- Collaborate with Business Development teams to identify target companies.
- Conduct competitive environment analysis.
- Develop account outreach plans.
- Research prospective pharmaceutical and biotechnology companies.
- Analyze business and financial news.
- Identify relevant decision-makers and influencers.
- Monitor competitors’ websites and marketing activities.
- Conduct market, competitor and product research.
- Support sales teams with relevant marketing collateral.
- Maintain CRM and sales enablement platforms.
- Ensure high standards of CRM data integrity.
- Generate weekly and monthly activity reports.
- Analyze market conditions, pricing and competitive positioning.
- Support lead identification and prospecting.
Qualification & Experience
Candidates should have a Bachelor’s degree in Marketing, Communications, Science, Business or a related discipline, or equivalent relevant experience.
Applicants should possess at least 6 months of experience across the product/service sales lifecycle, including client identification and prospecting.
Direct B2B sales experience within a service industry is expected.
Experience within the CRO, pharmaceutical or broader life sciences industry is preferred.
Knowledge of the CRO and specialty laboratory market, CRM platforms, business intelligence, competitive intelligence and pharmaceutical market research can be particularly valuable.
Why Consider Precision Medicine Group Careers?
These Precision Medicine Group jobs provide opportunities to work across specialized areas of clinical research and healthcare, including clinical quality assurance, clinical data management, clinical systems, data governance and life sciences competitive intelligence.
Depending on the position, successful candidates may gain exposure to international clinical research operations, regulated GxP environments, healthcare data, clinical technology platforms, pharmaceutical and biotechnology markets, and cross-functional global teams.
Specific compensation, employee benefits, insurance, leave, incentives and other employment benefits should be confirmed directly with Precision Medicine Group during the recruitment process.
How to Apply
Application Link For Quality Assurance Specialist III
Application Link For Senior Clinical Systems Administrator
Application Link For Content Analyst (Data Steward)
Application Link For Clinical Data Associate II
Application Link For Analyst, Business & Competitive Intelligence