Instagram
youtube
Facebook

Clinical Operation Spl

2+ years
Not Disclosed
10 Sept. 26, 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

Clinical Operation Specialist

Location: IND-Gurugram
Job ID: 25101767


Company Overview

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. They translate clinical, medical affairs, and commercial insights into actionable outcomes to address modern market needs.

The Clinical Development model places the customer and patient at the center of all operations, promoting simplified and streamlined processes while fostering collaboration and innovation.


Why Syneos Health

  • Career development and progression opportunities.

  • Supportive and engaged line management.

  • Technical and therapeutic area training.

  • Peer recognition and total rewards program.

  • Inclusive Total Self culture, promoting authenticity and belonging.

  • Focus on diversity of thoughts, backgrounds, and perspectives.


Job Summary

Roles within Clinical Operations at S11 level are responsible for safe and effective execution of clinical research studies. This includes:

  • Ensuring the wellbeing of research subjects.

  • Adherence to regulatory, health, and safety standards.

  • Coordination and communication with clinical trial volunteers and patients.

  • Collaboration with cross-functional teams to develop study materials, monitor trials, and resolve issues.


Key Responsibilities

Clinical Oversight & Participant Safety:

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

  • Review study protocols and execute procedures per protocol, regulatory, health, and safety standards.

  • Recruit, communicate with, and coordinate clinical trial volunteers and patients.

  • Monitor trial progress and resolve issues promptly.

Regulatory & Compliance:

  • Follow applicable regulations globally and by region.

  • Ensure all activities comply with local and international standards.

Collaboration & Study Support:

  • Collaborate with cross-functional teams to develop study materials (informed consent forms, study manuals, etc.).

  • Provide organizational and administrative support under supervision.

  • Perform routine tasks with flexibility to adapt to changing circumstances.

  • Utilize operational knowledge to improve study processes and outcomes.


Qualifications & Experience

Education:

  • High school diploma or equivalent required.

  • Associate’s degree or higher in a related field preferred.

Experience:

  • Minimum of 2 years 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.

Skills & Competencies:

  • 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

  • Posting is for a potential upcoming opportunity, not a live role. Expressing interest adds you to the talent pipeline.

  • Tasks and responsibilities may vary at the company’s discretion.

  • Syneos Health is committed to diversity, inclusion, and compliance with all applicable employment regulations.


Impact & Contribution

  • Ensure the safe and effective operation of clinical research studies.

  • Maintain the integrity and reliability of clinical trials.

  • Facilitate smooth study progress through coordination with volunteers, patients, and cross-functional teams.

  • Contribute to medical research and development of new treatments.


Core Focus Areas

  • Safeguarding research subjects.

  • Reviewing and executing study protocols.

  • Recruiting and communicating with trial participants.

  • Following global and regional regulations.

  • Collaborating to develop study materials.

  • Monitoring trial progress and resolving issues.

  • Providing organizational support and performing routine tasks.