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Project Manager - Clinical Research

Sun Pharma
5-10 years
INR 12-18 LPA
Mumbai, India
10 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Key Responsibilities

Clinical Project Management

  • Lead and manage clinical research projects from initiation to completion.

  • Develop project plans, timelines, milestones, and deliverables.

  • Monitor project progress and ensure achievement of study objectives.

  • Ensure projects are delivered on time, within scope, and within budget.


Team Leadership

  • Lead a team of clinical research professionals.

  • Assign responsibilities and monitor performance.

  • Mentor and support team development.

  • Foster collaboration across functional teams.


Resource & Budget Management

  • Plan and allocate project resources effectively.

  • Manage project budgets and financial tracking.

  • Monitor resource utilization and productivity.

  • Ensure cost-effective execution of clinical studies.


Vendor & Contract Management

  • Coordinate with procurement and finance teams.

  • Support vendor selection and outsourcing activities.

  • Oversee CRO and vendor performance.

  • Manage contracts and service agreements.


Risk Management

  • Identify project risks and operational challenges.

  • Develop mitigation and contingency plans.

  • Escalate critical issues appropriately.

  • Ensure proactive issue resolution.


Regulatory & Compliance Oversight

  • Ensure compliance with:

    • ICH-GCP Guidelines

    • Regulatory Requirements

    • Company SOPs

    • Clinical Trial Regulations

  • Oversee regulatory submissions and approvals.


Quality Management

  • Implement quality control processes.

  • Ensure data integrity and accuracy.

  • Monitor study compliance throughout the project lifecycle.

  • Support audit and inspection readiness.


Required Technical Skills

Clinical Research

  • Clinical Trial Management

  • Clinical Operations

  • Site Management

  • Monitoring Oversight

  • Vendor Management

  • Study Start-Up & Closeout

Project Management

  • Project Planning

  • Timeline Management

  • Risk Management

  • Resource Allocation

  • Budget Management

  • Stakeholder Management

Regulatory Knowledge

  • ICH-GCP

  • Ethics Committee Submissions

  • Regulatory Authority Submissions

  • Clinical Trial Regulations

  • Quality Management Systems


Required Soft Skills

  • Leadership & Team Management

  • Communication Skills

  • Strategic Thinking

  • Problem Solving

  • Decision Making

  • Negotiation Skills

  • Organizational Skills

  • Cross-Functional Collaboration


Preferred Certifications

  • Project Management Professional (PMP)

  • PRINCE2

  • Clinical Research Certifications

  • ICH-GCP Certification