Premier Research is hiring for two positions in its Clinical Data Sciences team: Data Coordinator – DM and Senior Data Coordinator – DM. These are full-time, hybrid opportunities based out of the company’s Bangalore office in India.
The openings are suitable for clinical data management professionals with experience in clinical research, clinical database management, EDC systems, data validation, query management, and Trial Master File (TMF) activities.
Candidates with experience in systems such as Medidata Rave, Calyx EDC, or DataLabs EDC can explore these opportunities.
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Premier Research Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Premier Research |
| Department | Clinical Data Sciences |
| Job Location | Bangalore, India |
| Work Mode | Hybrid |
| Employment Type | Full Time |
| Number of Positions | 2 Roles |
| Job Category | Clinical Data Management |
| Job Posting | November 4, 2026 |
Available Job Positions
1. Data Coordinator – DM
- Experience: Typically 2–4 years in Data Management or related clinical research industry experience.
- Qualification: Bachelor’s Degree or above, preferably in Life Sciences.
- CDMS Requirement: Knowledge of at least one Clinical Data Management System, such as Medidata Rave or Calyx EDC.
- Location: Bangalore
- Work Mode: Hybrid
Apply Online: https://premierresearch.wd12.myworkdayjobs.com/PremierResearch/job/India/Data-Coordinator_R7167/apply
2. Senior Data Coordinator – DM
- Experience: Minimum 4 years in Data Management or related clinical research industry experience.
- Qualification: Bachelor’s degree or above, preferably in Life Sciences.
- CDMS Requirement: Experience with at least two Clinical Data Management Systems, with in-depth knowledge of at least one, such as Medidata Rave or DataLabs EDC.
- Location: Bangalore
- Work Mode: Hybrid
Apply Online: https://premierresearch.wd12.myworkdayjobs.com/PremierResearch/job/India/Senior-Data-Coordinator_R7168/apply
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Job Responsibilities
Data Coordinator – DM
Selected candidates will be responsible for:
- Preparing clinical data management documentation, including CRF Completion Guidelines (CCGs), Data Management Plans (DMPs), and Data Report Specifications.
- Supporting standard test data development and performing User Acceptance Testing (UAT).
- Assisting with clinical database maintenance and updates.
- Performing clinical data entry and generating data review reports.
- Reviewing CRFs, data listings, and databases for protocol compliance.
- Generating and resolving data queries with investigational sites, CRAs, and client representatives.
- Performing external data and Serious Adverse Event (SAE) reconciliation.
- Supporting multiple studies as a Lead Data Coordinator and/or Safety Reviewer.
- Submitting documents to the Trial Master File (TMF) and supporting TMF QC activities.
- Performing database QC and quality checks of study reports and CRF archive files.
- Supporting project financial statistics, study metrics, dashboards, and project status reporting.
Senior Data Coordinator – DM
The Senior Data Coordinator will handle the following responsibilities:
- Preparing and maintaining clinical data management documentation, including CCGs, DMPs, Edit Check Specifications, and External Data Transfer Specifications.
- Supporting database testing, test data development, and User Acceptance Testing (UAT).
- Assisting with clinical database setup, maintenance, and updates.
- Reviewing CRFs, data listings, and clinical databases for accuracy and consistency.
- Managing data queries and resolving discrepancies with clinical research stakeholders.
- Performing external data and SAE reconciliation for moderately to highly complex studies.
- Acting as Lead Data Coordinator and/or Safety Reviewer across multiple studies.
- Managing TMF document submissions and supporting TMF Quality Control activities.
- Performing database QC and quality checks of study reports and eCRF PDF files.
- Supporting Data Scientists and Project Managers with study metrics, dashboards, financial statistics, and project reporting.
- Providing backup support for database setup activities.
- Coordinating activities according to study plans, project requirements, and timelines.
- Training and mentoring junior Data Coordinator team members.
- Serving as a subject matter expert for EDC systems and Data Coordinator activities.
Eligibility and Qualifications
Data Coordinator – DM
- Bachelor’s Degree or above, preferably in Life Sciences.
- Typically 2–4 years of Data Management or related clinical research industry experience.
- Knowledge of at least one CDMS, such as Medidata Rave or Calyx EDC.
Senior Data Coordinator – DM
- Bachelor’s degree or above, preferably in Life Sciences.
- Minimum 4 years of Data Management or related clinical research industry experience.
- Experience with at least two CDMS platforms.
- In-depth knowledge of at least one EDC system, such as Medidata Rave or DataLabs EDC.
- Familiarity with all phases of clinical studies, including database setup, maintenance, and database lock.
Required Skills and Technical Knowledge
Candidates applying for these positions should have relevant knowledge and experience in:
- Clinical Data Management (CDM)
- Clinical Data Management Systems (CDMS)
- Medidata Rave
- Calyx EDC
- DataLabs EDC
- Clinical Database Setup and Maintenance
- User Acceptance Testing (UAT)
- Edit Check Testing
- CRF Review and Data Validation
- Data Query Management
- SAE Reconciliation
- Trial Master File (TMF) and TMF QC
- Database Quality Control
Additional requirements for Senior Data Coordinator:
- Strong communication skills.
- Organizational and time management skills.
- Ability to manage multiple studies.
- Experience coordinating cross-functional study teams.
- Training and mentoring team members.
- Commitment to data quality and timely delivery.
