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.
FAQs
🏢 About the Employer
Syneos Health is a globally recognized organization providing integrated solutions across clinical development, data management, medical affairs, and commercialization. The company supports pharmaceutical and biotechnology clients worldwide and operates under strict quality and regulatory standards. Working at Syneos Health gives freshers exposure to global clinical research processes and structured data operations.
📊 Job Summary
- 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 Duties– 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.
🎓 Eligibility Requirements
Candidates applying for these future roles should meet the following:
- Educational background in Life Sciences, Pharmacy, Biotechnology, or related fields
- Basic understanding of clinical trials or clinical research concepts
- Willingness to learn clinical data management processes
- Ability to work in a structured and regulated environment
🧠 Core Skills
The following skills are beneficial for freshers applying to this role:
- Basic knowledge of clinical research and data handling
- Strong attention to detail and accuracy
- Analytical and logical thinking skills
- Good communication and documentation abilities
- Working knowledge of MS Office tools, especially Excel
- Ability to follow processes and instructions carefully
⭐ Job Overview
Clinical Data Associates play an essential role in ensuring the accuracy and reliability of clinical trial data. For freshers, this role provides a strong foundation in clinical research workflows, data quality principles, and compliance requirements. Exposure to real‑world clinical datasets prepares candidates for long‑term careers in clinical data management and research operations.
🎯 Best Fit Candidates
These future opportunities are suitable for:
- Fresh graduates in life sciences or pharmacy
- Candidates interested in clinical data or clinical research careers
- Individuals seeking entry‑level roles in global clinical organizations
- Freshers willing to learn structured data management processes
📈Future Growth
With experience and continuous learning, Clinical Data Associates can progress into roles such as:
- Clinical Data Associate II
- Clinical Data Analyst
- Senior Clinical Data Associate
- Clinical Data Lead or Project Support Roles
Syneos Health also provides training and development programs to support career growth.
💰 Salary Details
- Expected Salary: Salary range for this role is expected to be 3.5 to 4 LPA.
Salary may vary based on location, performance, and internal policies.
💡 Professional Tips
- Highlight attention to detail and analytical skills in your resume
- Learn basic concepts of clinical research and CDM
- Understand the importance of data accuracy in clinical trials
- Practice Excel skills relevant to data review
🔗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.
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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- Sun Pharma hiring for Clinical trial associate
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📚 Career Guide
❓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.
