IQVIA Hiring Senior Clinical Data Coordinator
- IQVIA Hiring Sr Clinical Data Coordinator in Thane & Kochi | Apply for Hybrid Clinical Data Management Role
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility & Qualifications
- Educational Background
- Experience & Skills
- Location & Employment Details
- Application Process
- Career Growth in Clinical Data Management
- Frequently Asked Questions (FAQs)
- 1. Is prior clinical data management experience mandatory?
- 2. Is this a remote position?
- 3. What key skills are required?
- 4. Does the role involve sponsor interaction?
- 5. What are future career prospects?
- Summary Table
IQVIA Hiring Sr Clinical Data Coordinator in Thane & Kochi | Apply for Hybrid Clinical Data Management Role
IQVIA is currently recruiting for the position of Sr Clinical Data Coordinator within its Clinical Data Management (CDM) department. This is a full-time hybrid opportunity based in Thane, India, with additional openings in Kochi. The role is designed for experienced clinical data management professionals who can lead complex studies, ensure high-quality data delivery, and support global clinical research operations.
This vacancy is ideal for candidates with a strong background in clinical data management, clinical database systems, and regulatory-compliant data handling who want to advance their career in a global clinical research organization.
Company Overview
entity[“organization”,”IQVIA”,”global healthcare analytics company”] is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences industry. Formed through the merger of IMS Health and Quintiles, IQVIA operates in more than 100 countries and supports pharmaceutical, biotechnology, and medical device companies in accelerating drug development and commercialization.
IQVIA combines advanced analytics, real-world evidence, and clinical trial management expertise to improve patient outcomes and population health worldwide. Its clinical data management teams play a critical role in ensuring data accuracy, regulatory compliance, and inspection readiness for global clinical trials.
The organization maintains strict ethical hiring standards and zero tolerance for fraud, reinforcing its reputation as a trusted partner in healthcare research and pharmaceutical services.
Job Role & Responsibilities
The Sr Clinical Data Coordinator will serve as a senior-level data management professional responsible for leading complex clinical studies and acting as the primary point of contact for designated data management tasks.
Core Responsibilities
- Act as Lead Data Management (DM) contact for assigned clinical research projects.
- Ensure all study deliverables meet defined quality standards and sponsor expectations.
- Participate in study kick-off meetings, internal audits, and sponsor inspections.
- Monitor and report data quality metrics and site-related issues to Data Management Team Leaders.
- Coordinate with clinical data management teams regarding timelines, database updates, and project status teleconferences.
- Ensure all Data Clarification Forms (DCFs) are resolved before database lock.
- Oversee data cleaning activities and ensure accurate data transfer to sponsors as per agreed specifications.
- Ensure study files are completed, archived, and maintained according to regulatory requirements.
- Mentor junior team members and support completion of mandatory training programs.
- Assist in database revisions and implementation of new clinical data technologies.
This position demands strong analytical skills, regulatory awareness, and the ability to manage multiple global clinical trial datasets simultaneously while maintaining high-quality standards.
Eligibility & Qualifications
Educational Background
Candidates must hold a Bachelor’s degree in Clinical Sciences, Biological Sciences, Mathematical Sciences, or a related field.
Relevant qualifications include:
B.Pharm, M.Pharm, BSc Life Sciences, MSc Life Sciences, BSc Biotechnology, MSc Biotechnology, BSc Microbiology, MSc Microbiology, BSc Biostatistics, MSc Biostatistics, BSc Mathematics, MSc Mathematics, BSc Statistics, MSc Statistics, Clinical Research, Biomedical Sciences, or equivalent combination of education and experience.
Experience & Skills
- Proven experience in Clinical Data Management or related clinical research roles.
- Strong understanding of clinical trial data lifecycle and database management.
- Knowledge of MS Office applications including Word and Excel.
- Familiarity with clinical applications, programming or macro knowledge is an advantage.
- Excellent organizational and communication skills.
- Ability to resolve data discrepancies independently.
- Capability to build effective working relationships with clients, sponsors, and internal teams.
Candidates with prior experience handling database lock activities, sponsor audits, and cross-functional clinical data coordination will be well suited for this leadership-level position.
Location & Employment Details
- Primary Location: Thane, India
- Additional Location: Kochi, India
- Employment Type: Full-Time
- Work Model: Hybrid
- Job Requisition ID: R1521376
Compensation is aligned with industry benchmarks for senior clinical data management professionals. IQVIA offers structured career progression, exposure to multinational sponsors, and performance-driven growth opportunities within clinical research services.
Application Process
Interested candidates can apply directly through IQVIA’s official career portal using the link below:
Applicants are encouraged to submit accurate and complete information as IQVIA maintains strict compliance and verification standards during recruitment.
Career Growth in Clinical Data Management
Senior Clinical Data Coordinators play a critical role in ensuring clean, validated, and regulatory-compliant clinical trial data. With the rapid expansion of global clinical trials and increased regulatory scrutiny, demand for experienced clinical data management professionals continues to grow.
This role can lead to opportunities such as Data Team Lead (DTL), Associate Data Team Lead (ADTL), Clinical Data Manager, or Global Data Management Lead within multinational pharmaceutical and biotechnology organizations.
Professionals in this domain contribute directly to accurate clinical trial outcomes, regulatory approvals, and safe commercialization of innovative therapies.
Frequently Asked Questions (FAQs)
1. Is prior clinical data management experience mandatory?
Yes, candidates must have relevant experience in clinical data management or equivalent exposure in clinical research.
2. Is this a remote position?
No, this is a hybrid role based in Thane or Kochi, India.
3. What key skills are required?
Strong data management expertise, communication skills, regulatory understanding, and proficiency in MS Office tools are essential.
4. Does the role involve sponsor interaction?
Yes, the Sr Clinical Data Coordinator interacts with sponsors and participates in audits and project review meetings.
5. What are future career prospects?
This role provides a pathway to Data Team Lead, Clinical Data Manager, and global leadership positions in clinical research.
Summary Table
| Company | IQVIA |
| Vacancies | Sr Clinical Data Coordinator |
| Required Education | B.Pharm, M.Pharm, BSc/MSc Life Sciences, Biotechnology, Microbiology, Biostatistics, Mathematics, Statistics, Clinical Research |
| Experience | Clinical Data Management experience required |
To apply for this job please visit jobs.iqvia.com.
