Back to Job SearchROLE OVERVIEW
An exciting opportunity for a Strategic Feasibility Lead to join a leading pharmaceutical and biotech organization’s clinical development team. This role is based within the Program Delivery team of our client’s Global Clinical Sciences & Operations (GCSO) division, supporting the successful execution of global clinical trials across phases 1 to 4.
As a key member of the team, you will leverage your expertise to oversee feasibility activities, collaborate with CROs and internal stakeholders, and ensure efficient study planning and site selection. This position offers the chance to make a significant impact on clinical development strategies in a dynamic, innovative environment.
KEY DUTIES AND RESPONSIBILITIE
Your duties as the Strategic Feasibility Lead will be varied however the key duties and responsibilities are as follows:
-
Conduct, oversee, and synthesize internal and external data to develop meaningful feasibility solutions that support clinical programs and studies.
-
Support clinical planning activities at the program and study level, including accurate recruitment forecasting to ensure timely trial delivery.
-
Collaborate with CRO feasibility teams and internal stakeholders from early engagement through to country and site selection, ensuring alignment and consensus.
-
Coordinate with stakeholders to build consensus around planning processes and support ad-hoc inquiries related to feasibility.
-
Contribute to the development and improvement of feasibility tools and approaches, supporting continuous enhancement of site and country selection strategies.
-
Ensure all feasibility activities adhere to industry best practices, guidelines, and regulatory requirements.
-
As the Strategic Feasibility Lead, you will identify opportunities for process improvements that enhance trial delivery, site engagement, and participant recruitment.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Strategic Feasibility Lead we are looking to identify the following on your profile and past history:
-
A Degree or higher level in a relevant field (e.g., Pharmaceutical Sciences / Clinical Research / Biotechnology).
-
Proven track record of at least 5 years in the pharmaceutical, biotech, or CRO industry, with experience in clinical planning and/or project management.
-
Experience working on cross-functional projects within a global environment.
-
Knowledge of GCP guidelines across different regions and experience in clinical trial feasibility or site strategy roles.
WHAT’S IN IT FOR YOU?
Joining our client’s team offers you the opportunity to work on impactful clinical programs within a forward-thinking organization. You’ll be part of a dynamic environment that values innovation, offers professional growth, and supports a collaborative culture. This is a pivotal role for those looking to influence global clinical development strategies and hone their leadership skills.
Key Words: clinical / feasibility / project management / global environment / GCP guidelines / clinical trials / site selection / regulatory compliance / biotech / pharmaceutical / * CRO* / clinical development / collaborative / stakeholder engagement / continuous improvement
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career."
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
