A leading global CRO, PRA is transforming clinical trials through our people, innovation and transparency. We serve clients across all phases of pharmaceutical and biotech drug development by combining therapeutic and operational expertise with local knowledge
PRA’s commitment to excellent in research begins with our people. Our workforce has grown by over 25% since 2010 and now comprises over 4,700 employees spanning more than 13 time zones and speaking more than 15 languages.
It is our philosophy that the way in which we grow our business is to focus on our employees and as such, we recognize that successful careers are found within organisations that provide the support that employees need at work, as well as the benefits they require outside the office.
Post: Clinical Team Manager
Job description
As a Clinical Team Manager you will create and maintain all relevant clinical project documents, and tools pertinent to the phase of the study, ensuring compliance with company, applicable regulatory and customer requirements. You will need to ensure consistent implementation of PRA methodologies during the different phases of the study.
You will serve as the primary liaison and primary point of escalation for clinical activities and team issues, interacting with clients, vendors and other PRA functional areas. You will work with the Project Manager to build and foster the client relationship and provide data as required for clinical performance metrics and project status metrics - applying and drawing conclusions between project activities/deliverables and project metrics and initiating measure to improve metrics. You will liaise with Clinical Operations Managers to resolve resource and performance issues and contribute to Business Development activities participating in proposals and bid defenses as needed.
Candidate Profile:
The successful candidate will have an undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution or a licensed health-care professional (i.e., registered nurse). You will have substantial experience using computerised information systems, Outlook, Word, Excel, PowerPoint, and CTMS. You will have thorough knowledge of ICH GCP and an awareness of local regulatory authority regulations regarding drug research and development required. You must have a considerable amount of experience in clinical research with experience of managing clinical projects.
Together with a competitive salary, we offer a comprehensive range of benefits and an excellent working environment. As we continue to expand, there will be career opportunities on a truly global scale.
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