Proclinical Staffing

Contract Clinical Program Director

Location
Homeworking
Salary
Up to £750 per day
Posted
10 Jun 2021
Closes
24 Jun 2021
Ref
38143
Contact
Matthew Pike
Hours
Full Time
Contract Type
Contract
Experience Level
Senior Management
An exciting opportunity has arisen for a contract Clinical Program Director to lead a Global Project Team. You will work with the development team to design operational inputs but also develop programme strategy.

Job Responsibilities

Plans, directs and delivers the operational components of assigned clinical programs from design concept to final CSR, through to study closed and archived within agreed budget, time, quality and aligned KPIsLeads and delivers differentiated and robust operational options for review at Investment Decision Governance interactionsLeads operational discussions with external entities including regulatory agencies, preferred partners/suppliers and external collaboratorsDevelops and maintains effective program level risk management/mitigation plans to ensure timely delivery to quality and budgetAccountable for planning and leading issue escalation and resolution Accountable for the acquisition of clinical trial data from internal and external sources Input to the study delivery related activities associated with regulatory inspections/audits in liaison with Clinical Quality Assurance Accountable for the quality of study delivery planning information into relevant planning systemsAccountable for coordination of selection of external providers for programme/study specific tasksProvision to procurement of clear specifications for program/study specific outsourcingReview and operational approval of program/study specific contracts or work ordersOperational management and oversight of external providers at program/study levelEngagement with preclinical and translational science as well as statistics and regulatory in order to design and deliver robust clinical development plans. Skills and Requirements

Minimum BA/BSc At least three years' relevant experience in clinical development including team leadership. Experience or capability to manage in-house and/or outsourced regional or global Phase 1, 2 or 3 studies from study start-up to study report completion. A SrCPM must have substantial experience in study management in different indications and proven ability to manage complex multinational studies or multiple simultaneous studies from start to end.

To Apply

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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