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Safety Specialist Ii - Clinical Trial Exp (Must Have) - Hybrid

0-2 years
Not Disclosed
10 Nov. 11, 2025
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Safety Specialist II – Clinical Trial Experience (Hybrid)

Location: Salem, India (Hybrid)
Updated: October 31, 2025
Job ID: 25102440
Company: Syneos Health®


About Syneos Health®

Syneos Health is a global, fully integrated biopharmaceutical solutions organization focused on accelerating customer success. With over 29,000 employees across 110 countries, we support the development, launch and commercialization of new therapies by combining clinical, medical affairs, and commercial insights.

We believe in simplifying processes, improving efficiency, and creating a workplace where employees feel valued and supported through career development, training, and our inclusive Total Self Culture.


Why Work With Us

  • Strong focus on career development, training and progression

  • Supportive and engaged line management

  • Diverse and inclusive workplace culture

  • Recognized globally for supporting the development of:

    • 94% of FDA-approved novel drugs (past 5 years)

    • 95% of EMA-authorized products

    • 200+ clinical studies across 73,000 sites and 675,000+ trial patients


Role: Safety Specialist II – Clinical Trial Experience

This position requires hands-on experience with clinical trial safety and involves working in a hybrid model from our Salem location.


Key Responsibilities

(Note: Syneos states that responsibilities may vary based on business needs.)

  • Support Safety and Pharmacovigilance (PV) activities for clinical trials

  • Perform safety case processing and assessments

  • Ensure compliance with global regulatory requirements

  • Collaborate with cross-functional clinical and medical teams

  • Support documentation, reporting, and continuous improvement processes

  • Maintain high-quality standards and timelines

  • Contribute to patient safety and risk management activities


Additional Information

  • Responsibilities listed are not exhaustive; additional tasks may be assigned.

  • Equivalent education or experience may be considered.

  • The company ensures compliance with all equal employment and disability inclusion laws including ADA provisions.

  • This description is not an employment contract.