Ref #: 28080

Employment type: Permanent - Full-Time

Location: South Africa

Posted: 31-Mar-2021

Description

In this role you will be accountable for day to day activities for the management of company-sponsored Infectious Disease/Tropical Disease studies, including study plans, timelines, resources, allocation and management of product (re-) supply, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams

- You will oversee all studies, including the support of the set-up and operational assessment of investigator-sponsor, tracking performance and payments according approved plan, managing product supply, if applicable, coordinating internal review of final report

- You will manage CROs, clinicians, independent CRAs, or statisticians when required by the project including selection, coordination of project specific training, and payment
- Develop and monitor study budget and timelines and monitor work to ensure quality

- Ensures that trial status is tracked and maintained in the CTMS t
- Participate in the planning and set-up of a study and provide planning parameters

- Manage the budget for all local clinical studies and Global Phase IV studies assigned, as well as the IST/ISS grants.

You will need;

• At least 3 years of clinical trial management/project management experience gained in a CRO, pharma or biotech company
• Experience in clinical trial planning and conduct
• Thorough knowledge of ICH GCP and applicable local regulations

Please get in touch at alison.burton@docsglobal.com as soon as possible, to arrange a call for the next step in your career