Syneos Health is hiring for the positions of Drug Safety Specialist I / II in Hyderabad and Gurugram. This is a full-time, permanent opportunity for candidates with experience in pharmacovigilance and Individual Case Safety Report (ICSR) processing.
The role involves end-to-end safety case processing across spontaneous, clinical trial and literature cases. Selected candidates will work on activities including case triage, data entry, medical coding, narrative writing, submission readiness and quality checks while following applicable pharmacovigilance procedures and regulatory requirements.
Syneos Health Drug Safety Specialist Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Syneos Health |
| Position | Drug Safety Specialist I / II |
| Job Location | Hyderabad / Gurugram |
| Experience | 1–6 Years |
| Employment Type | Full Time, Permanent |
| Job Function | Drug Safety / Pharmacovigilance |
| Role Category | Health Informatics |
| Industry | Clinical Research / Contract Research |
| Qualification | BDS, B.Pharm, BHMS / MDS, M.Pharm |
| Salary | Not Disclosed |
About Syneos Health
Syneos Health is a global organization working across clinical research, healthcare and life sciences services. The company supports pharmaceutical and biotechnology organizations through clinical development, commercialization and related healthcare services.
This Drug Safety Specialist position falls within the clinical informatics and pharmacovigilance area, with a focus on processing and maintaining safety case information.
Job Description
The Drug Safety Specialist I / II will be responsible for processing Individual Case Safety Reports (ICSRs) throughout the applicable case workflow.
The position covers cases originating from spontaneous reports, clinical trials and literature sources. Depending on experience and performance, the role may also involve quality-control review of processed safety cases.
Key Responsibilities
ICSR Case Processing
- Process Individual Case Safety Reports from receipt through submission readiness.
- Handle spontaneous, clinical trial and literature safety cases.
- Perform case triage according to applicable workflows.
- Enter and maintain accurate case information in the relevant safety systems.
- Ensure case information is complete and appropriately documented.
Data Entry and Case Management
- Perform accurate data entry activities, particularly during the initial phase of the role.
- Review available case information and identify relevant data.
- Maintain accurate records throughout the case-processing workflow.
- Follow established procedures for handling and documenting safety information.
Medical Coding
- Perform required coding activities as part of ICSR processing.
- Apply applicable coding conventions and established pharmacovigilance procedures.
- Ensure coded information is accurately reflected in the safety case.
Narrative Writing
- Prepare case narratives as required.
- Ensure narratives accurately represent the available safety information.
- Maintain appropriate quality and consistency in case documentation.
Submission Readiness
- Process cases through the required workflow to support submission readiness.
- Ensure case information and documentation meet applicable procedural and regulatory requirements.
- Follow established timelines and workflow requirements.
Quality Control
- Perform quality checks on processed cases where applicable.
- QC responsibilities may depend on the candidate’s experience and performance.
- Identify processing errors and support appropriate corrections.
- Maintain quality standards throughout case-processing activities.
Pharmacovigilance and Compliance
The position requires adherence to:
- Global pharmacovigilance guidelines
- Company Standard Operating Procedures (SOPs)
- Applicable regulatory requirements
- Established case-processing procedures
- Quality standards for safety reporting
Candidates should understand the importance of accuracy, completeness and consistency when handling safety information.
Educational Qualification / Eligibility Criteria
The vacancy accepts candidates with the following educational backgrounds:
Undergraduate Qualifications
- BDS – Bachelor of Dental Surgery
- B.Pharm – Bachelor of Pharmacy
- BHMS – Bachelor of Homeopathic Medicine and Surgery
Postgraduate Qualifications
- MDS – Master of Dental Surgery
- M.Pharm – Master of Pharmacy
Candidates should have a relevant healthcare, pharmaceutical or medical education background.
Experience Requirements
The job listing specifies an experience range of 1–6 years.
The role is particularly relevant to candidates with experience in:
- Pharmacovigilance
- Drug safety
- ICSR processing
- Clinical safety
- Case processing
- Safety data management
The provided listing does not separately specify different experience requirements for Drug Safety Specialist I and Drug Safety Specialist II.
Required Skills
Candidates should have capabilities relevant to:
- ICSR processing
- Pharmacovigilance case management
- Case triage
- Safety data entry
- Medical coding
- Narrative writing
- Case quality review
- Regulatory compliance
- SOP adherence
- Attention to detail
- Accurate documentation
- Case workflow management
Strong accuracy and the ability to follow defined processes are important for safety case-processing activities.
Work Location and Job Type
Locations: Hyderabad and Gurugram, India
Employment Type: Full Time, Permanent
The provided job listing does not specify whether the position is remote, hybrid or office-based.
Salary / CTC
The salary for the Drug Safety Specialist I / II position has not been disclosed in the provided job listing.
Candidates should confirm compensation details during the recruitment process.
Selection Process
The detailed selection process is not specified in the provided vacancy. Candidates should follow the recruitment process communicated by Syneos Health and complete any applicable interview or assessment stages.
How to Apply for Syneos Health Drug Safety Specialist Recruitment 2026
Interested candidates can apply through the recruitment listing where the position is advertised.
Applicants should review the complete job requirements and submit an updated CV highlighting relevant pharmacovigilance or drug-safety experience.
Important Details Before Applying
- Syneos Health is hiring for Drug Safety Specialist I / II.
- Job locations include Hyderabad and Gurugram.
- The listed experience range is 1–6 years.
- The employment type is full-time and permanent.
- The role focuses on pharmacovigilance and ICSR case processing.
- Cases may include spontaneous, clinical trial and literature reports.
- Responsibilities include triage, data entry, coding, narrative writing and submission readiness.
- Quality-control activities may be assigned based on experience and performance.
- Candidates with BDS, B.Pharm, BHMS, MDS or M.Pharm qualifications are listed as eligible.
- Salary is not disclosed in the provided listing.
Frequently Asked Questions
1. What position is Syneos Health hiring for?
Syneos Health is hiring for Drug Safety Specialist I / II.
2. Where are these jobs located?
The positions are listed for Hyderabad and Gurugram.
3. What is the required experience?
The job listing specifies 1–6 years of experience.
4. What qualifications are accepted?
The listed qualifications include BDS, B.Pharm, BHMS, MDS and M.Pharm.
5. What type of cases will the Drug Safety Specialist handle?
The role involves spontaneous, clinical trial and literature cases.
6. What does the case-processing workflow include?
The workflow includes triage, data entry, coding, narrative writing and preparation of cases for submission.
7. Is pharmacovigilance experience relevant?
Yes. The role is focused on drug safety and pharmacovigilance case-processing activities.
8. Does the position involve quality control?
Yes. Quality checks may be performed based on the candidate’s experience and performance.
9. Is this a permanent position?
Yes. The listing describes the employment type as Full Time, Permanent.
10. What is the salary for this position?
The salary has not been disclosed in the provided job listing.
11. Is the role remote or hybrid?
The provided listing identifies Hyderabad and Gurugram as locations but does not specify a remote or hybrid arrangement.
Important Note
Job availability, eligibility requirements, location, experience criteria and recruitment conditions may change. Candidates should verify the latest information on the employer’s official careers channel before applying.