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Project Manager - Clinical Research

Sun Pharma
5-10 years
INR 12-20LPA
Mumbai, India
10 June 15, 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, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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

Key Responsibilities

Project Leadership & Management

  • Lead and manage a team of clinical research professionals.

  • Collaborate with cross-functional stakeholders to drive project success.

  • Develop and implement comprehensive project plans, timelines, milestones, and resource strategies.

  • Define project objectives, deliverables, and success criteria in alignment with stakeholder expectations.

Resource & Budget Management

  • Allocate resources effectively and assign project responsibilities.

  • Monitor team performance and project deliverables.

  • Develop and manage project budgets.

  • Track project expenses and ensure cost-effective utilization of resources.

  • Ensure projects remain within approved budget parameters.

Risk Management

  • Identify potential project risks and challenges.

  • Develop mitigation and contingency plans.

  • Monitor project progress and proactively address issues impacting timelines or quality.

Vendor & Contract Management

  • Partner with finance and procurement teams to manage vendor selection and contracting activities.

  • Oversee outsourced activities and ensure vendor performance meets project expectations.

Regulatory Compliance & Quality Assurance

  • Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and applicable regulatory requirements.

  • Oversee preparation and submission of regulatory documentation to ethics committees and regulatory authorities.

  • Implement quality control measures to maintain data integrity, accuracy, and compliance.

  • Ensure inspection readiness and adherence to internal SOPs.

Stakeholder Management

  • Communicate project status, risks, and milestones to internal and external stakeholders.

  • Facilitate collaboration across clinical operations, regulatory affairs, data management, biostatistics, and other functional teams.


Educational Qualifications

Required

  • Bachelor's or Master's Degree in:

    • Life Sciences

    • Biology

    • Pharmacology

    • Nursing

    • Healthcare

    • Clinical Research

    • Related Scientific Discipline

Preferred

  • Post-Graduate Diploma in Clinical Research or equivalent qualification.


Experience Requirements

  • Minimum 5–10 years of relevant experience in Clinical Research.

  • Experience managing clinical studies and cross-functional project teams.

  • Strong understanding of clinical trial operations and regulatory requirements.

  • Experience in budget management, vendor oversight, and project planning preferred.


Required Skills & Competencies

Technical Skills

  • Clinical Trial Management

  • Project Planning & Execution

  • GCP & ICH Guidelines

  • Risk Management

  • Budget & Resource Management

  • Regulatory Documentation

  • Vendor Management

  • Quality Assurance & Compliance

Leadership Skills

  • Team Leadership

  • Stakeholder Management

  • Decision Making

  • Conflict Resolution

  • Strategic Planning

Soft Skills

  • Excellent Communication Skills

  • Strong Organizational Abilities

  • Analytical Thinking

  • Problem Solving

  • Collaboration & Teamwork