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Clinical Trial Manager

ICON
2+ years
Not Disclosed
Bangalore, India
10 May 28, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Trial Manager

Company

ICON plc – A global healthcare intelligence and clinical research organization focused on accelerating the development of innovative medicines and improving patient outcomes.


Job Details

  • Job Title: Clinical Trial Manager (CTM)

  • Job Requisition ID: JR149652

  • Employment Type: Full-time

  • Work Mode: Office (Non-Flex)

  • Location: Bangalore, India


About the Role

ICON is seeking a Clinical Trial Manager (CTM) to oversee and manage clinical trial operations across assigned studies.

In this role, you will be responsible for ensuring that clinical trials are executed efficiently, within timelines, budget, and regulatory requirements, while maintaining high-quality standards and strong stakeholder collaboration.


Key Responsibilities

1. Clinical Trial Planning & Execution

  • Plan and manage all aspects of clinical trials.

  • Ensure adherence to:

    • Timelines

    • Budget

    • Quality standards

2. Cross-functional Coordination

  • Collaborate with internal teams to:

    • Develop and implement study protocols

    • Define trial procedures

  • Ensure alignment across clinical operations functions.

3. Stakeholder Management

  • Build and maintain strong relationships with:

    • Investigators

    • Study sites

    • Internal and external stakeholders

4. Regulatory & Compliance Oversight

  • Ensure all clinical trials comply with:

    • Local regulations

    • National regulations

    • International guidelines

    • Ethical standards (including ICH-GCP)

5. Decision-making & Risk Management

  • Support decision-making related to:

    • Trial design

    • Vendor selection

    • Risk mitigation strategies

  • Identify and resolve operational challenges.


Required Qualifications

Education

  • University degree in:

    • Medicine

    • Life Sciences

    • Or equivalent combination of education and experience

Experience

  • Demonstrated ability to manage clinical trial deliverables.

  • Prior experience in clinical monitoring is preferred.

Skills & Competencies

  • Strong clinical trial management experience.

  • Ability to manage multiple priorities effectively.

  • Strong problem-solving and decision-making skills.

  • Subject matter expertise in a relevant therapeutic area.

  • Ability to lead and coordinate cross-functional teams.


Additional Requirements

  • Willingness to travel approximately 25% of the time.


Rewards & Benefits

ICON offers a competitive benefits package, which may include:

  • Competitive salary

  • Health insurance for employees and families

  • Retirement and savings plans

  • Life assurance coverage

  • Employee wellness and assistance programs

  • Flexible benefits (gym memberships, travel support, childcare options, etc.)

  • Paid annual leave

Benefits vary depending on role and location.


Inclusion & Accessibility

ICON is committed to fostering an inclusive and accessible workplace where all employees are valued.

All applicants are considered equally regardless of background, identity, or disability.

Reasonable accommodations are available during the recruitment process upon request.