Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Career Opportunities: Manager - Clinical Feasibility (10684)

Successfactor
Successfactor
1-8+ years
preferred by company
10 Feb. 11, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Manager – Clinical Feasibility

Location: Gurgaon, Tower B (Floor 11), India
Company: Confidential / Leading Life Sciences Organization
Date Posted: February 9, 2026
Employment Type: Full-Time
Industry: Clinical Research | Drug Development | Clinical Operations


About the Role

We are seeking a Manager – Clinical Feasibility to lead the strategic assessment and planning of clinical trials. The role focuses on protocol evaluation, patient recruitment analysis, and site selection to optimize trial design and execution. You will collaborate closely with Business Development, Clinical Operations, and Global Project Leads to deliver data-driven feasibility insights for both pre-award and post-award studies.

The ideal candidate brings a strong understanding of clinical trial operations, feasibility analytics, and therapeutic area expertise, along with leadership experience in mentoring junior staff and ensuring regulatory compliance.


Experience Required

  • 8+ years of experience in drug development, with minimum 1 year specializing in clinical feasibility, site identification, or patient recruitment planning

  • Proven experience in global clinical study planning, protocol assessment, and operational strategy


Educational Qualification (Mandatory)

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related scientific discipline


Key Responsibilities

Strategic Feasibility Analysis

  • Lead comprehensive feasibility assessments for clinical trials, including:

    • Patient recruitment modeling

    • Country and site selection

    • Protocol evaluation and risk assessment

Proposal Support

  • Provide operational input and strategic recommendations to Business Development teams

  • Assess risks and identify strategies to improve bid success for clinical trials

Data & Technology Utilization

  • Leverage clinical databases, patient registries, and digital analytics tools

  • Validate feasibility assumptions and identify potential trial risks and bottlenecks

Stakeholder Management

  • Collaborate with Global Project Leads, Clinical Operations, external partners, and sponsors

  • Ensure alignment of feasibility outputs with organizational objectives

Leadership & Quality Assurance

  • Mentor and guide junior feasibility team members

  • Ensure compliance with ICH-GCP guidelines and regulatory requirements

  • Maintain high-quality standards in all feasibility deliverables and outputs


Required Skills & Competencies

  • Strong knowledge of clinical trial design, therapeutic areas, and operational strategy

  • Expertise in patient recruitment planning, site feasibility, and trial risk assessment

  • Proficiency in clinical databases, data visualization tools, and feasibility modeling

  • Excellent analytical, communication, negotiation, and project management skills

  • Leadership skills with the ability to mentor junior staff and drive team performance

Core Competencies

  • Strategic Thinking & Agility

  • Process Excellence & Data-Driven Decision Making

  • Collaboration & Stakeholder Management

  • Result Orientation & Accountability

  • Innovation & Problem Solving


Why Join?

  • Play a key role in global clinical trial planning and execution

  • Work with cross-functional teams across Clinical Operations, Business Development, and Global Project Management

  • Gain exposure to strategic feasibility, patient recruitment modeling, and site selection for high-impact clinical studies

  • Develop leadership skills in a dynamic, regulated life sciences environment


Equal Opportunity Statement

We are committed to providing equal employment opportunities across recruitment, compensation, promotion, and professional development. All qualified candidates will be considered in accordance with applicable regulatory and employment standards.