Hobson Prior currently having an exciting opportunity for a Global Study Lead to join a leading pharmaceutical organisation who provide pioneering medicines to patients all over the world. This position will work from home initially with eventually working 1-2 days in the office.

Job Responsibilities:

• Accountable to lead, provide guidance and delegate appropriately to a cross-functional study team or oversee outsourced delivery activities to ensure the clinical study progresses as planned, driving achievement of milestones according to timelines, budget and quality standards.
• Ensure all external service providers engaged at the study level are performing to contracted goals and timelines/budget. Ensure adequate oversight is documented and any issues are escalated appropriately.
• Lead and facilitate communication across all functions. Lead and conduct investigator meetings and other study related meetings.
• You will provide input into and hold accountability for the development of essential study documents in accordance with relevant company SOPs.
• Develop and maintain relevant study plans as well as detailed and realistic study timelines.
• Responsible for ensuring that all systems utilized at a study-level (e.g. ACCORD, PharmaCM, etc.) are maintained.
• Accountable for leading the identification of overall study-level risk management activities. Ensure mitigation strategies are implemented effectively and that issue escalation pathways are clear to the entire study team.
• To oversee study level performance against agreed upon plans, milestones and key performance indicators. Communicate key risks and proposed mitigations to applicable stakeholders.
• Maintain oversight over quality issue reporting in accordance with relevant company SOPs and collaborate with all functions and/or external service providers as necessary to implement corrective and preventative actions.
• Oversee Trial Master File completion from study start until archiving, in accordance with relevant company's SOPs.
• Any other assigned duties.

Requirements:

• A minimum of 3 years+ experience in leading studies.
• Exposure to working on global studies - 2-4 studies at any one time
• Excellent PM skills.
• Previous experience of leading early phases studies (1-3).
• Vendor Management - selecting vendors, stakeholder management.
• Therapy area: CVRM (Cardiovascular, Renal and Muscular).

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.