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As a contract Study Manager, you will be assigned to pRED early phase clinical studies, working as part of a cross-functional study team to deliver study management and clinical operations activities under the guidance of a pRED Study Management Team Leader.
Please note that applicants must have the right to work in this location to be considered.
What you will be doing:
* Deliver Study Execution: Provide operational expertise in protocol design, feasibility, country selection, patient-centricity, and data delivery plans, ensuring study quality and integrity through proper documentation and systems.
* Provide Country Oversight: Support or manage feasibility assessments, guide country operational teams, and ensure timely study start-up and recruitment.
* Manage Vendor Performance: Oversee relationships with vendors and third-party suppliers, ensuring compliance with standards and performance expectations.
* Plan Demand and Supply: Oversee forecasting and maintenance of supplies, including IMP, to support clinical sites.
* Manage Risk and Compliance: Assist in identifying and mitigating study-related risks, overseeing logs and documentation.
* Drive Operational Excellence: Contribute to improving and standardizing operational activities across studies.
Who are you:
You are talented, passionate, and inspired by our mission. You thrive in collaborative, patient-centric, and entrepreneurial environments.
* You possess a growth mindset and are eager to learn from experience.
* You are comfortable in fast-paced, ambiguous, and collaborative settings.
* You hold a university degree or equivalent experience, preferably in life sciences.
* You have demonstrated strong performance as a Study Manager or similar role in the pharmaceutical or healthcare industry, with drug development experience preferred.
* You are a self-starter passionate about achieving successful outcomes and delivering excellence.
* You are eager to innovate and challenge conventions.
* You have a good understanding of the drug development process and relevant regulations, including ICH and GCP guidelines.
For more information, please contact Grant Van Schalkwyk.
If interested, please click 'Apply' or visit the 'Contact Us' page to speak with one of our specialists.
Hobson Prior is a leading life sciences recruiter, acting as an employment agency for this vacancy.
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