Company Description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job Description
Our team is searching for a relationship pro, dedicated to connecting with sites to advance clinical trials in the best way. Sounds like you're the expert we're searching for?
Hybrid in Pretoria
You will:
- Maintain and generate relations with Investigative Sites.
- Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement.
- Participate in the development of improvement strategies for the site identification process, implementation thereof, as well as related training activities.
Project Responsibilities:
- Define the main study objectives and the optimal site profile.
- Create initial list of potential sites.
- Communicate with project teams on project/ regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use.
- In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities.
- Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives.
- In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites.
- Participate in project team meetings during study startup, as needed.
- Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed.
Qualifications
- University/college degree (Life Sciences/Pharmacy/RN/Healthcare field is a plus), or an equivalent combination of education, training and experience.
- Minimum 10 years of proven prior experience in Site Identification/Feasibility/Study Start-Up activities/Site Monitoring.
- Understanding of Good Clinical Practice, local laws and applicable regulations in the region.
- Full working proficiency in English.
- Communication and collaboration skills.
- Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements.
Additional Information
We offer:
- Excellent working conditions.
- Extensive training and friendly team.
- Competitive salary and benefits package.
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
What We Do
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas.
PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines.
PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world.
PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees.
http://www.psi-cro.com
