Study Manager – 1 year FTC

Roche

Study Manager managing early phase clinical studies at Roche, delivering study execution and ensuring quality and compliance in operations.

Posted 7/8/2026contractWelwyn • 🇬🇧 United KingdomMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in study execution, operational excellence, and risk management within the pharmaceutical and healthcare sectors. Proficient in drug development processes and regulatory compliance, ensuring study quality and integrity.

Highest-signal resume keywords

Study ManagementDrug Development ProcessICH GuidelinesGCP GuidelinesVendor Performance Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Protocol DesignFeasibility AssessmentData Delivery PlanningRisk ManagementSupply ForecastingStudy DocumentationOperational Expertise

Soft Skills

CollaborationProblem SolvingAdaptability

Industry Keywords

Pharmaceutical IndustryHealthcare IndustryClinical StudiesPatient Centricity

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Deliver study execution by providing operational expertise into protocol design and feasibility, country selection, patient centricity and data delivery plans
Ensure study quality and integrity by developing and maintaining study systems and documentation
Provide country oversight for insourced studies
Manage vendor performance by providing direction and actively managing relationships
Plan demand and supply by overseeing the forecasting and maintenance of supplies needed for clinical studies
Manage risk and compliance by assisting the study team in identifying, managing and mitigating study-related risks
Drive operational excellence by providing operational expertise across operations-related activities

Requirements

What you’ll need

Hold a university degree or equivalent years of experience (preferred focus in life sciences)
Strong and consistent performance as a Study Manager or equivalent in pharmaceutical and/or healthcare industry
Drug development experience (therapeutic area experience a plus)
Strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines
Able to think on your feet and thrive in fast-paced, ambiguous and highly collaborative environments

Benefits

Comp & perks

1-year fixed-term contract
Opportunity to work in a collaborative, patient-centric environment
Scientific rigor and innovation in drug development