Contract Senior Manager, Global Trial Optimization - Contract - Remote within US
Proclinical is seeking a Temporary Senior Manager for Global Trial Optimization.
Primary Responsibilities:
This role involves leading program or study level activities to inform the clinical development strategy, clinical study concepts, study protocols and operational plans. The successful candidate will play a key role in developing and maintaining relationships with external experts to facilitate a wide source of country and disease area intelligence that can be utilized in study design and operational planning.
Skills & Requirements:
- A minimum of a Bachelors' degree and relevant industry experience.
- Direct working history managing clinical trial operations, including experience developing protocols and key study documents.
- Knowledge of ICH/GCP and regulatory guidelines/directives.
- Exceptional interpersonal & leadership skills.
- Expert knowledge and a data-driven approach to planning, executing, and problem-solving.
- Advanced communication skills via verbal, written and presentation abilities.
- Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization.
- Advanced project management skills, cross-functional team leadership and organizational skills.
- Technical proficiency in trial management software and MS applications.
The Contract Senior Manager of Global Trial Optimization's responsibilities will be:
- Lead study level feasibility processes to generate high-quality data for study design, optimal geographical placement, and operational planning.
- Partner with teams during CRO led feasibility activities to support validation of study and country level enrolment rates and study start-up timelines.
- Support the development and implementation of the Global Trial Optimization function through process initiatives and change management activities.
- Partner with Data and Analytics function to review and identify appropriate central data sources.
- Lead study level engagements to obtain, analyze and deliver high-quality targeted information from external stakeholders.
- Lead study level activities to generate and deliver patient level insights.
- Provide input into a range of continuous improvement activities to ensure consistency of Global Trial Optimization process execution.
- Partner with study teams to develop and implement patient recruitment and retention tactics aligned with defined study strategy.
If you are having difficulty in applying or if you have any questions, please contact Matthew Pike at m.pike@proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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