Why This Role Stands Out
Advance your career in clinical research with PSI CRO, a global company that prioritizes its people and drives medical innovation, by taking ownership of challenging study activation processes. This hybrid role is ideal for detail-oriented individuals eager to develop their skills in a supportive environment and contribute to bringing life-changing medicines to patients. Apply now to join a passionate team and make a tangible impact on global health.
Quick Overview
Job 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 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
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.
Take your career to the next level and lead challenging study activation process on a country level. You will support clinical research teams and ensure PSI projects start smoothly and on time.
You will:
- Perform study startup activities and support all processes critical for site activation
- Collect site documents for IRB/IEC submission and/or IP-RED process
- File study-specific documentation in TMF, in accordance with Document management plan
- Assist in feasibility research and site identification, upon request
- Facilitate site agreement and budget negotiations
- Coordinate translation and review of study-specific documents
- Identify and escalate project-specific issues as needed
- Prepare and submit IP-REDs packages
- Ensure initial distribution of locally obtained clinical study supplies to sites and supervises initial distribution of Investigational Product(s) and centrally obtained clinical study supplies to sites
- Ensure exchange of information and documentation with investigational sites, off site facilities and vendors
- Participate in development of site-specific startup timelines and enrolment projections and is responsible for meeting the site activation targets under supervision
- College/University degree in Life Sciences or an equivalent combination of education, training and experience
- At least 2 years of full-scope Study Startup experience in the country/region
- Full working proficiency in English
- Well-developed communication and organizational skills
- Ability to negotiate and build relationships at all levels
We offer:
- Excellent working conditions
- Extensive training and friendly team
- Competitive salary and benefits package
- Opportunities for personal and professional growth
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.
Similar jobs
- PM
In Vivo Study Specialist
Parabilis Medicines
Cambridge🇬🇧$75k - $85k/yr2 weeks agoHTTPS - RE
Director, Clinical Pharmacology
Recursion
London🇬🇧£118.3k - £136.5k/yr2 weeks agoHealthcare - IH
Clinical Regulatory Specialist
Iterative Health
NYC🇬🇧1 week agoGCPSpringClinical Research+4 - IH
Senior Clinical Regulatory Specialist
Iterative Health
NYC🇬🇧1 week agoGCPSpringClinical Research+7 - FP
Pioneering Medicines: Associate Director / Director, Clinical Operations
Flagship Pioneering, Inc.
Cambridge🇬🇧$148k - $236.5k/yr2 weeks agoGCPClinical TrialsCompliance+10 - CA
Clinical Lead - New Products
Careers at Eucalyptus
UK - HQ - London🇬🇧1 week agoClinical ResearchHTTPHTTPS+2