Clinical Feasibility Leader

Parexel

. Act as the functional lead responsible for site identification activities across all study types and phases .

Posted 11/6/2026full-timeRemote • United Kingdom, Hungary, Georgia, Netherlands, Switzerland, Denmark, Finland, Sweden, Spain, Turkey, Belgium, Serbia, IrelandSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial management, including site identification strategies, feasibility assessments, and enrollment modeling. Proficient in presenting findings and recommendations to stakeholders while leading cross-functional teams in a matrix environment.

Highest-signal resume keywords

Clinical Research ExperienceSite Identification StrategiesFeasibility AssessmentsStrategic ThinkingProject Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Protocol-Specific Site IdentificationEnrollment Scenario ModelingData AnalysisSurvey DesignCountry Selection Analysis

Soft Skills

Interpersonal CommunicationLeadershipProblem-SolvingFlexibilityAttention to Detail

Tools & Technologies

Feasibility SystemsClinical Trial Management Tools

Industry Keywords

International Clinical TrialsPatient RecruitmentStakeholder EngagementMatrix EnvironmentSponsor Liaison

About the role

Key responsibilities & impact

Act as the functional lead responsible for site identification activities across all study types and phases
Develop and implement protocol-specific site identification strategies
Design protocol-specific site questionnaires and analyze investigator responses
Lead locally assigned teams to deliver prequalified sites, including training, survey launch, and issue escalation
Deliver revised enrollment scenarios and final lists of prequalified sites
Prepare slide decks and integrated reports presenting site selection outcomes, methodology, results, and recommendations
Revise protocol feasibility assessments and country selection analyses using post-award data
Manage country clinical operations surveys and compile data into country selection analyses, scenario modeling, and site identification strategies
Contribute to optimized operational strategies for patient recruitment and enrollment scenarios
Present and defend country/site selection strategies and enrollment models in internal and Sponsor meetings
Act as Project Leader on stand-alone feasibility studies under management supervision, including Sponsor liaison, project initiation, resource planning, implementation, milestone tracking, progress reporting, and communication management
Attend Bid Defense and Sponsor Kick-Off Meetings and present feasibility/prequalification services
Serve as Subject Matter Expert for an identified feasibility system, tool, or process

Requirements

What you’ll need

Relevant clinical research experience in management of international clinical trials, feasibility, and recruitment
Demonstrated clear understanding of country and site feasibility requirements
Previous exposure to development of clinical trial strategy, modeling of enrollment scenarios, and selection of countries/sites
Strong strategic thinking and analytical skills applied to business needs
Excellent interpersonal, verbal, and written communication
Demonstrated leadership and ability to influence others
Problem-solving skills allowing client-focused approach to work
Flexible attitude with respect to work assignments and new learning
Ability to prioritize workload with attention to detail
Willingness to work in a matrix environment and value teamwork
Ability to work independently and in a decentralized reporting model
Fluent in written and spoken English

Benefits

Comp & perks

Home based work from select EMEA locations