Syneos Health Hiring Fresher for Clinical Data associate- Future roles

Syneos Health, a global biopharmaceutical solutions organization, is inviting applications for Clinical Data Associate – Future Roles on a remote basis. This opportunity is suitable for B.Pharm and M.Pharm graduates with 0–2 years of experience who are interested in building a career in clinical data management and clinical research operations.

These positions are part of Syneos Health’s Talent Pipeline, created to identify and pre‑screen candidates for upcoming Clinical Data Associate openings. By applying, candidates will be considered for future hiring needs and contacted when relevant opportunities become available.

This is a strong early‑career opportunity for professionals seeking exposure to global clinical trials, data quality processes, and regulated clinical research environments while working remotely.

Job Overview

Position: Clinical Data Associate
Department: CDM
Location: Remote, India(Expected)
Experience: 0-2 years
Qualification: B.Pharm, M.Pharm
Job Type: Full-Time
Last Date of application: Not provided

Key Responsibilities – Clinical Data Associate

Study Setup & Compliance
- Maintain awareness of contract scope and deliverables for assigned projects.
- Review and follow study‑specific Clinical Data Management Plans (CDMPs) and applicable SOPs.
Data Entry & System Access
- Receive and enter laboratory normal ranges into the clinical database.
- Complete and submit CDMS access requests, forms, and required spreadsheets.
Discrepancy & Query Management
- Review edit checks, discrepancy outputs, and validation listings generated from the clinical database.
- Raise queries or apply self‑evident corrections as per the Data Validation Specification (DVS) and Data Management Plan (DMP).
- Review resolved queries, close appropriately, or re‑query when required.
Paper Study Support
- Review completed Data Clarification Forms (DCFs) and update CRFs and databases as applicable.
- Perform internal QC checks by comparing database listings against CRFs and DCFs.
- Ensure timely return of CRFs and DCFs to the Document Control Room (DCR) per project guidelines.
Hybrid & EDC Study Support
- Serve as backup for data entry activities for paper and hybrid studies.
- Pre‑review CRFs prior to scanning and perform QC checks using image‑based systems.
- For EDC studies, perform data management quality reviews and internal QC checks as required.
Project Tracking & Reporting
- Assist in tracking study progress and milestones per project timelines.
- Prepare and distribute periodic status reports to support project oversight.
Database Lock & Study Close‑Out
- Support activities related to database finalization, data transfer, and delivery of project documents to the sponsor.
- Assist in achieving scheduled study milestones and close‑out activities.
Documentation & Archival
- Create electronic storage media for EDC studies in accordance with SOPs.
- File project documentation in the Data Management Study File (DMSF).
- Support study archival activities as per organizational requirements.
Training & Process Knowledge
- Maintain proficiency in data management systems and processes through regular training (e.g., CDA Knowledge College).
- Understand the coding process and the purpose of interim analysis, dry runs, and data cuts.
Meetings & Audits: Participate in internal meetings and support internal or external audits as required.

Required Skills & Qualifications

Educational Background: BA/BS degree in Biological Sciences or a related Natural Science / Healthcare discipline.
Clinical Data Management Knowledge
- Preferred experience or exposure to Clinical Data Management (CDM) practices and relational database systems.
- Familiarity with Oracle Clinical, Medidata Rave, Inform, or similar systems is an advantage.
Clinical & Regulatory Understanding
- Basic knowledge of clinical data, ICH guidelines, and Good Clinical Practice (GCP) standards.
- Familiarity with medical terminology is preferred.
Technical Skills
- Proficiency in MS Windows, Microsoft Word, Excel, and email applications.
- Good keyboard speed and accuracy for data entry and documentation tasks.
Industry Experience (Preferred): Prior experience or exposure in clinical research, drug development, data management, or a healthcare environment is preferred.
Communication & Interpersonal Skills
- Strong written and verbal communication skills, with the ability to inform, influence, and collaborate effectively.
- Good presentation and interpersonal abilities for working within cross‑functional teams.
Organizational & Work Skills
- Strong planning, organizational, and time‑management skills.
- Ability to multitask under tight deadlines while maintaining attention to detail.
- Flexibility to adapt to change and work independently or within multidisciplinary teams.
Compliance & Professional Accountability
- Ability to perform activities in compliance with Corporate Business Practices, SOPs, and Work Instructions.
- Willingness to undertake other responsibilities as assigned by management.
Travel Requirement: Minimal travel may be required (up to 25%) based on project needs.

Why Join Syneos Health

Career Development & Growth
Syneos Health is committed to developing its people through clear career paths, continuous learning, technical and therapeutic‑area training, and opportunities for long‑term progression.
Supportive Leadership & Recognition
Work in an environment with supportive and engaged line management, peer recognition, and a comprehensive total rewards program that values individual contributions.
Total Self Culture
Syneos Health promotes a Total Self culture, where employees are encouraged to bring their authentic selves to work. This inclusive culture connects teams globally and focuses on employee well‑being.
Inclusive & Diverse Workplace
The company values diversity of thought, background, culture, and perspective, fostering a workplace where everyone feels included and respected

How to Apply

Interested candidates should apply only through the official company career website using the link provided below. By applying, candidates will be considered for future hiring needs and contacted when relevant opportunities become available.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.

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FAQ – Clinical Data Associate

1. What does “Future Roles / Talent Pipeline” mean?

These are pre‑hiring positions created to identify and shortlist candidates for upcoming Clinical Data Associate openings. Selected profiles will be contacted when relevant roles become available.

2. Who can apply for these future roles?

Candidates with a B.Pharm or M.Pharm degree and 0–2 years of experience or freshers with interest in clinical data management are eligible to apply.

3. Is this suitable for freshers?

Yes. This opportunity is ideal for freshers and early‑career professionals looking to build a career in Clinical Data Management and clinical research operations.

4. Is this a permanent job opening?

These are talent pipeline roles, not immediate openings. Applying helps you get pre‑screened for future hiring opportunities at Syneos Health.

5. Is this role fully remote?

Yes. These future roles are intended to support remote working, depending on project and business requirements.