Summary
Location
Warsaw
Type
contract
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About this role
Company Description
PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
This position is a fixed-term contract for 12 months, with the possibility of extension.
As a Study Startup Assistant, you'll have the chance to gain valuable experience in Clinical Trials by engaging in a dynamic Study Startup process, all while learning from our supportive and professional team. Your key responsibilities will include:
- Providing administrative support to the Startup department in processes critical for site activation.
- Supporting the Feasibility department with research and site identification activities.
- Maintaining project-specific tracking systems and electronic Trial Master File (eTMF) throughout the study startup phase.
Qualifications
- College or University degree or an equivalent combination of education
- Minimum of 1 year experience in an administrative role
- Native Polish and Very Good English skills
- Excellent communication and interpersonal skills
- Attention to detail
- Ability to work in a team or independently
Additional Information
We offer:
- Stability, long-term cooperation
- Permanent contract, full-time job
- Competitive salary and benefit package
- Excellent working conditions
- Opportunities for personal and professional growth
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
Other facts
About PSI CRO
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
What you'll do
- The Study Startup Assistant will provide administrative support to the Startup department for site activation processes and assist the Feasibility department with research and site identification activities. Key duties also involve maintaining project-specific tracking systems and the electronic Trial Master File (eTMF) during the study startup phase.
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