Syneos Health Recruitment 2026: Safety & PV Specialist Jobs
Syneos Health Recruitment 2026: Safety & PV Specialist Jobs in Gurugram
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(Syneos Health Recruitment 2026) |
Syneos Health has published a recruitment listing for Safety & PV Specialist positions under Pharmacovigilance (PV), with night-shift requirements and office-based work in India. The opportunity may be relevant to experienced pharmacy and medical graduates who have practical knowledge of Individual Case Safety Report (ICSR) processing, medical coding, safety databases, and regulatory safety reporting.
According to the supplied job details, Safety & PV Specialist I candidates should have approximately 2.6 years or more of pharmacovigilance experience, while the broader recruitment listing also describes separate experience requirements for Specialist II and Senior Specialist positions. Eligible educational backgrounds include B.Pharm, M.Pharm, BDS, BMS, and MBBS. B.Sc. and M.Sc. qualifications are excluded from the listed eligibility criteria.
The role involves processing and reviewing safety cases, maintaining accurate pharmacovigilance records, coding medical information, supporting regulatory reporting, and following applicable quality procedures. Candidates must be comfortable working night shifts and attending the designated office.
Important recruitment update: The official Syneos Health listing describes this opportunity as a possible upcoming role and talent-pipeline opportunity rather than necessarily a confirmed active vacancy. Candidates should check the official application page to confirm the current status before applying.
Syneos Health Recruitment 2026: Job Overview
| Particulars | Details |
|---|---|
| Company | Syneos Health |
| Job Role | Safety & PV Specialist (SS I) |
| Department | Pharmacovigilance / Drug Safety |
| Job Location | Gurugram, Haryana, as provided in the vacancy details |
| Work Mode | Office-based |
| Employment Type | Full-time |
| Shift | Night shift |
| Experience | 2.6–4 years, depending on the specialist level |
| Educational Qualifications | B.Pharm, M.Pharm, BDS, BMS, MBBS |
| Job Requisition ID | 25110762 |
| Joining Preference | Immediate or early joiners preferred |
| Salary | Not specified in the supplied job details |
| Interview Date | Not announced in the supplied details |
| Application Method | Online through the official company careers page |
Candidates should verify the exact location and experience level displayed in the live application form because the official listing may cover more than one specialist grade or office location.
About Syneos Health
Syneos Health is a global biopharmaceutical services organization that supports pharmaceutical and biotechnology companies across clinical development, medical affairs, and commercialization. Its work connects scientific, clinical, and commercial expertise to help clients develop and bring therapies to patients.
The organization supports activities across different stages of the medicine development lifecycle, including clinical trials, regulatory-related services, medical affairs, and pharmacovigilance operations.
Company Headquarters and Establishment
Syneos Health's corporate headquarters is located at 1030 Sync Street, Morrisville, North Carolina 27560, United States.
The company's present identity was established in 2017 following the merger of INC Research and inVentiv Health. Its predecessor, INC Research, began in 1998. Therefore, 2017 refers to the formation of Syneos Health under its current name, while the organization draws on a longer history of predecessor businesses.
Employee Strength
Syneos Health reports a global workforce of more than 26,000 professionals, operating across more than 60 countries, according to its corporate overview. Employee figures can change over time, so this should be treated as the company's reported workforce scale rather than a fixed headcount.
Why Is Syneos Health Relevant to Pharmacovigilance Professionals?
Pharmacovigilance is an important part of medicine safety monitoring. Pharmaceutical companies and their service partners must collect, evaluate, document, and report relevant safety information according to applicable requirements.
A role with a biopharmaceutical services organization may provide exposure to structured safety operations, case-processing workflows, quality review, medical coding, and regulatory reporting processes. The precise responsibilities and training available depend on the assigned project and position.
Official company website: https://www.syneoshealth.com/
Position Details: Safety & PV Specialist (SS I)
The Safety & PV Specialist I role supports pharmacovigilance operations by helping ensure that individual safety cases are processed accurately, documented correctly, and handled within applicable timelines.
Individual Case Safety Reports, commonly called ICSRs, contain information about suspected adverse events associated with medicines or other relevant health products. Pharmacovigilance teams evaluate these reports, record the available information, code medical terms, assess completeness, and support reporting obligations.
The position requires an understanding of safety case workflows, attention to detail, appropriate documentation, and compliance with project-specific procedures.
This role is particularly relevant to professionals who already have hands-on PV experience and want to continue developing their expertise in case processing, medical coding, quality review, and safety reporting.
Key Responsibilities of a Safety & PV Specialist
The following responsibilities are based on the supplied vacancy details and the official job description.
1. Individual Case Safety Report Processing
The specialist processes ICSRs according to Standard Operating Procedures (SOPs), project requirements, and applicable safety-processing guidelines. This includes reviewing the available case information and ensuring that it is entered accurately into the relevant system.
2. Safety Database Management
The role involves entering safety information into pharmacovigilance databases and tracking systems. Accurate data entry is essential because errors or missing information can affect downstream safety assessments and reporting activities.
3. Case Completeness and Reportability Assessment
The specialist helps evaluate whether a case contains the required information, identifies missing details, and supports assessment of regulatory reportability according to applicable procedures.
4. Medical Coding and MedDRA
Medical coding involves converting reported medical information into standardized terminology. Depending on the case, this may include adverse events, medical history, concomitant medications, and medical tests.
Knowledge of MedDRA terminology is particularly useful for candidates applying to roles involving adverse-event coding and safety data review.
5. Narrative Writing and Follow-up
The role may involve preparing clear case narratives and identifying information that requires follow-up. Queries may be raised to obtain missing or unclear information, with the aim of improving case completeness and accuracy.
6. Regulatory Safety Reporting
The specialist supports the preparation and processing of safety reports according to relevant regulatory requirements and project timelines. Timeliness, completeness, and adherence to established procedures are important in this area.
7. Literature Screening and Review
Literature screening helps identify potentially relevant safety information from scientific publications. The work may include reviewing literature, identifying relevant cases, and processing information according to the applicable workflow.
8. Product and Drug Coding Activities
The position may involve drug coding, drug-dictionary maintenance, identification of duplicate ICSRs, and manual recoding of relevant product or substance terms.
9. xEVMPD and SPOR/IDMP Activities
The vacancy mentions validation and submission of xEVMPD product records, including indication coding, as well as SPOR/IDMP-related activities. Candidates with experience in these specialized regulatory data processes may find this aspect particularly relevant.
10. Quality Review and Documentation
The role includes quality review of ICSRs and maintenance of relevant documentation. Depending on the project, records may need to be maintained in the Trial Master File (TMF) or Pharmacovigilance System Master File (PSMF), as applicable.
11. Compliance and Audit Support
The specialist is expected to follow relevant SOPs, work instructions, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, Good Pharmacovigilance Practices (GVP), and applicable regulations. Participation in audits and professional coordination with project teams may also be required.
Eligibility Criteria for Syneos Health PV Jobs
Candidates should carefully review the educational, experience, location, and shift requirements before submitting an application.
Educational Qualifications
The listed qualifications are:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
- Bachelor of Dental Surgery (BDS)
- BMS, as specified in the recruitment listing
- Bachelor of Medicine, Bachelor of Surgery (MBBS)
B.Sc. and M.Sc. qualifications are explicitly excluded from the listed eligibility criteria.
Candidates should ensure that their actual degree title matches the accepted qualifications in the official application form. Applicants with a different qualification should not assume eligibility based only on a related Life Sciences background.
Required Pharmacovigilance Experience
Experience requirements differ according to the specialist grade described in the official listing:
- Safety & PV Specialist I: Minimum 2.6 years of PV experience.
- Safety & PV Specialist II: Minimum 4 years of PV experience.
- Senior Safety & PV Specialist: Minimum 6 years of PV experience; the senior listing also specifies ICSR case-processing and quality-check or quality-review experience.
The supplied vacancy summary refers to 2.6–4 years for the target role. Candidates should select the grade that matches their actual experience and verify the criteria on the official job page.
Location and Shift Requirements
The vacancy details provided specify office-based work in Gurugram, Haryana. The official recruitment listing may include other office locations for the broader hiring requirement, so candidates should confirm the location attached to the position they select.
Applicants must be willing to work night shifts. Candidates should consider their travel arrangements, shift preferences, and ability to work from the assigned office before applying.
Joining Availability
Immediate and early joiners are preferred according to the supplied job details. This preference does not guarantee selection, and applicants should provide an accurate joining timeline.
Skills Required for This Pharmacovigilance Position
Candidates with the following skills and knowledge may be better prepared for the responsibilities described in the vacancy.
ICSR case processing: Practical understanding of case intake, triage, data entry, case narratives, follow-up, and case completion.
MedDRA medical coding: Familiarity with standardized medical terminology and the correct coding of reported adverse events and other medical information.
Safety database experience: Ability to enter, review, and track safety information accurately within the relevant database or workflow system.
Quality review: Knowledge of checking case completeness, consistency, coding accuracy, and compliance with applicable procedures.
Regulatory reporting awareness: Understanding of reporting timelines, reportability assessments, and the importance of following project-specific instructions.
Literature screening: Ability to review scientific publications for potentially relevant safety information.
Documentation and data integrity: Maintaining complete and accurate records while following established procedures.
Communication skills: Clear written communication, appropriate query handling, and professional collaboration with internal and external teams.
Regulatory and quality knowledge: Familiarity with SOPs, GCP, ICH guidance, GVP, and relevant drug-safety regulations.
Applicants should list only those skills and systems they genuinely understand or have used professionally.
Salary and Compensation
The supplied recruitment details do not specify an official salary or compensation range for the Safety & PV Specialist I role.
Compensation may vary according to the specialist grade, years of experience, relevant technical skills, work location, and the company's applicable compensation structure. Candidates should confirm salary, shift allowance, benefits, and other employment terms directly during the official recruitment process.
It would be misleading to present an unverified salary estimate as an official Syneos Health package.
Interview Details
The supplied job description does not provide a confirmed interview date, interview time, or interview venue.
Candidates should apply through the official careers page and monitor communications from the company's recruitment team. If shortlisted, they should follow the interview instructions shared by the recruiter.
Depending on the employer's process, candidates may be assessed on their PV experience, ICSR processing workflow, medical coding, case quality, regulatory reporting knowledge, and ability to work night shifts. These are preparation suggestions based on the role, not a confirmed interview-round schedule.
Documents to Prepare Before Applying
The supplied job listing does not provide a definitive document checklist. However, candidates can prepare the following commonly useful documents for an online application and potential recruitment stages:
- Updated professional resume or CV.
- Educational certificates and mark sheets.
- Experience certificates or other legitimate employment records, if available.
- A record of relevant pharmacovigilance responsibilities and technical skills.
- Government-issued identity documents, if requested through the official recruitment process.
- Any additional documents specifically requested by the recruiter.
Make sure your resume accurately reflects your total PV experience, ICSR processing responsibilities, medical coding knowledge, quality-review exposure, and notice period or joining availability.
Do not send sensitive identity or financial documents to unofficial contacts. Share personal documents only through verified company channels and when they are required.
How to Apply for Syneos Health Recruitment 2026
Candidates can use the official online recruitment page provided for this position.
Step 1: Open the Official Application Page
Visit the Syneos Health job listing:
Step 2: Verify the Current Status
Check whether the application page is accepting applications for an active vacancy or collecting profiles for a possible upcoming opportunity. Confirm the position title, location, specialist grade, and experience requirements.
Step 3: Review Your Eligibility
Check that your degree, pharmacovigilance experience, and relevant technical skills match the selected grade. Remember that the listed eligibility excludes B.Sc. and M.Sc. qualifications.
Step 4: Submit Your Application
Follow the instructions on the official careers portal. Enter your details accurately and upload your current resume or any other requested documents.
Step 5: Monitor Recruitment Communication
Check your registered email and the official application portal for updates. Respond to genuine recruiter communications and verify that messages claiming to represent Syneos Health come from legitimate company channels.
Important: The official listing describes this as a possible upcoming opportunity rather than necessarily a live vacancy. Submitting your details may place you in the talent pipeline; it does not guarantee an interview or selection.
Frequently Asked Questions (FAQs)
1. What is the job role announced by Syneos Health?
The recruitment listing covers Safety & PV Specialist positions in Pharmacovigilance, including Specialist I and other experience-based grades. The supplied target role is Safety & PV Specialist I.
2. What is the required experience for Safety & PV Specialist I?
The official listing specifies a minimum of 2.6 years of pharmacovigilance experience for Safety & PV Specialist I. Higher specialist grades require additional experience.
3. Which qualifications are accepted for this PV job?
The listed qualifications are B.Pharm, M.Pharm, BDS, BMS, and MBBS. B.Sc. and M.Sc. are explicitly excluded from the stated eligibility criteria.
4. Is this a work-from-home job?
No. The supplied vacancy details describe the role as office-based. Candidates should verify the specific office location on the official application page.
5. Is night-shift availability mandatory?
Candidates must be willing to work night shifts according to the recruitment details.
6. What are the main responsibilities of the Safety & PV Specialist?
Responsibilities include ICSR processing, safety database entry, case completeness assessment, medical coding, narrative writing, follow-up, regulatory safety reporting, literature screening, quality review, and relevant documentation.
7. What is the salary for this position?
The supplied job details do not specify the salary. Candidates should confirm compensation and any applicable shift allowance directly through the official recruitment process.
8. Has Syneos Health announced an interview date?
No interview date or venue is provided in the supplied details. Candidates should follow the official recruitment portal and any verified communication from the company.
9. Are immediate joiners preferred?
Yes. Immediate and early joiners are preferred according to the supplied recruitment information.
10. Is the vacancy confirmed to be actively hiring?
The official listing describes the opportunity as a possible upcoming role and talent-pipeline opportunity. Candidates should check the live application page to confirm whether applications are being accepted for an active opening.
Conclusion
Syneos Health's Safety & PV Specialist recruitment listing may be relevant to experienced pharmacovigilance professionals seeking opportunities in ICSR processing, medical coding, safety database management, regulatory reporting, and quality review.
Candidates with B.Pharm, M.Pharm, BDS, BMS, or MBBS qualifications should carefully compare their experience with the requirements for Specialist I, Specialist II, or Senior Specialist positions. Practical PV experience, accurate case processing, MedDRA knowledge, quality awareness, and the ability to work night shifts are important considerations for this role.
Before applying, confirm the current recruitment status, office location, experience criteria, and compensation through the official Syneos Health careers page. Keep your resume accurate, prepare examples of your relevant work experience, and use only verified application channels.
Disclaimer: This article is intended for job-information and career-awareness purposes. Job status, eligibility, location, salary, and recruitment procedures may change. Candidates should verify all details through the official company website before applying.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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