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Clinical Operation Spl

2+ years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time 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

Job Title:

Clinical Operation Spl

Location:

Gurugram, Haryana, India

Company:

Syneos Health®

Job ID:

25101767


Position Overview:

Ensures the safe and effective operations of clinical research studies. Safeguards research subject wellbeing, oversees protocol adherence, and coordinates study activities in compliance with regulatory, health, and safety standards.


Key Responsibilities:

  • Safeguard the wellbeing of research subjects in a medical capacity.

  • Review study protocols and execute procedures in alignment with protocols and regulatory standards.

  • Recruit and maintain communication with clinical trial volunteers and patients throughout the study.

  • Ensure compliance with applicable regulations globally and regionally.

  • Collaborate with cross-functional teams to develop study materials, including informed consent forms and study manuals.

  • Monitor trial progress and address any operational or protocol-related issues promptly.

  • Provide organizational support, including administrative assistance as needed.

  • Perform routine tasks with adaptation as required to changing circumstances.

  • Apply broad knowledge of operational systems and clinical practices to improve study outcomes.


Qualifications:

  • High school diploma or equivalent required; Associate’s degree or higher in a related field preferred.

  • Minimum 2 years of experience in clinical operations or related field.

  • Strong understanding of clinical research protocols and regulatory requirements.


Certifications:

  • Certified Clinical Research Coordinator (CCRC) or equivalent preferred.

  • Basic Life Support (BLS) certification required.


Necessary Skills:

  • Excellent communication and interpersonal skills.

  • Strong organizational and time management abilities.

  • Attention to detail and accuracy in documentation.

  • Ability to work effectively in a team environment.

  • Proficiency in Microsoft Office Suite and clinical trial management software.


Additional Information:

  • Tasks and responsibilities may evolve according to project requirements.

  • Supports Syneos Health’s culture of diversity, inclusion, and career development.

  • Posting may represent a potential upcoming opportunity; interested candidates may be added to the talent pipeline.


Summary:

Clinical Operations roles at the S11 level ensure the safe and efficient conduct of clinical research studies. Responsibilities include protecting research subjects, protocol review, volunteer/patient coordination, regulatory compliance, cross-functional collaboration, and study monitoring. These roles significantly contribute to the success and integrity of clinical trials, supporting smooth study execution and the advancement of medical research.