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Global Study Lead (FSP) at Lifelancer · ApplyPick

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Global Study Lead (FSP)

Global Study Lead (FSP)

LifelancerUnited States only

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Opens the original posting on Himalayas.

Apply now Source: Himalayas

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Job Title: Global Study Lead (FSP)
Job Location: Remote, India
Job Location Type: Remote
Job Contract Type: Full-time

Job Seniority Level:

Work Schedule

Standard (Mon-Fri) Environmental Conditions

Office Job Description

Global Study Lead – This position is a fully client-embedded role, dedicated to a leading bio-pharma company.

Role Purpose:

This GSL is a single accountable person and a Clinical Operations representative. Will drive operational strategy, planning and leading the study and being aligned with the asset strategy. The GSL and GSM work s a leadership-operational duo.

Key Responsibilities:

Overall Study Leadership
Own the day-to-day management of the global clinical study
Lead cross-functional study teams (clinical operations, data management, biostatistics, medical monitoring, regulatory, supply chain, safety, etc.)
Ensure alignment between global strategy and regional execution
Drive study timelines, milestones, and deliverables
Study Planning and Execution

Develop and maintain:

study timelines operational plans risk management plans enrollment strategies
Oversee country start-up, site activation, recruitment, monitoring, and closeout
Ensure protocol execution is consistent globally
Vendor and CRO Oversight
Manage external vendors and CRO partners
Track performance metrics and service quality
Resolve operational issues and escalations
Ensure vendors meet contractual obligations and timelines
Budget and Resource Management
Monitor study budgets and forecasts
Track study spend against plan
Identify resource gaps and operational risks
Support financial governance and change management
Risk and Issue Management
Identify study risks early
Lead mitigation and contingency planning

Handle escalations related to:

recruitment delays protocol deviations data quality issues supply shortages inspection readiness
Regulatory and Quality Compliance

Ensure study conduct follows:

ICH-GCP local regulations
SOPs protocol requirements
Support inspection readiness and audit activities

Oversee CAPAs when needed

Cross-Functional Communication
Serve as the central operational contact for the study

Communicate updates to:

senior leadership study teams regional teams sponsors/partners
Lead governance meetings and study reviews
Data and Study Oversight
Monitor enrollment, data cleaning, query resolution, and database lock readiness

Review KPIs and operational metrics

Ensure timely delivery of quality data
Strategic Decision-Making
Make operational decisions that impact study delivery
Balance quality, speed, cost, and patient safety
Recommend process improvements and efficiencies

Education Requirements:

Bachelor’s degree: life sciences or related discipline; The role will require a good understanding of complex clinical development and regulatory processes.

Role Related Experience:

At least 15+ years of relevant study management experience on a global level .
In-depth experience in clinical research: study management, monitoring, data management

Previous in-depth Oncology experience

Must have exposed to clinical study management “end-to-end” Globally : NA, EMEA, APAC, LATAM – China & Japan, Africa is an asset –
Must have proven experience from study feasibility to CSR
Must have at least Ph II and PIII experience – PI & PIV is an asset
Must have cross-functional leadership proven experience, able to drive internal and external meeting
Able to input in clinical protocol, ICF, and other study plan, savvy in clinical study risk management and clinical systems
Strong experience in clinical budget management
Strong experience with vendor management including CRO
Exposed to competent authority Inspections (FDA, EMA, MHRA, PMDA...), being involved in studies pivotal for drug file registration is an asset

Fluent in English, to the level they can negotiate and discuss (adapt message) related to complex topics with any Clinical team member (Local country representative, Statistician, Data Manager, laboratory, central laboratory, Scientific writer, safety representative, study Phycician and any type of vendors as well as able to present clear status to upper management if required.

Excellent stakeholder management and communication skills (oral and written), outstanding interpersonal skills.

Demonstrates leadership skills, promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives Strong understanding of the clinical study, drug development, sample management and other associated process and quality requirements, including ICH/GCP guidelines and SOPs Good project management skills (including scope, budget, timeline, and resource planning and management, and use of associated tools and support where available) This job is curated by Lifelancer .

Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Please apply via Lifelancer platform to get connected to the application page and to find similar roles.
Originally posted on Himalayas

Apply now

Opens the original posting on Himalayas.

Apply now Source: Himalayas

Apply now

Opens the original posting on Himalayas.

Apply now Source: Himalayas

About the job

Apply before: Dec 3, 2026
Posted on: Oct 4, 2026
Job type: Full Time
Experience level: Senior
Location requirements: United States
Hiring timezones: Worldwide
Skills: Clinical Operations Lead Clinical Project Manager Clinical Research Manager Clinical Study Lead Clinical Study Manager FSP Trial Lead Global Clinical Trial Lead Global Study Manager Study Lead

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