Clinical Project Manager
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PSI CRO
US
Summary
The Clinical Project Manager will lead full-service clinical research projects in phases II and III, ensuring deliverables are met on time and within budget. They are also responsible for mentoring project teams, supporting business development activities, and maintaining compliance with company standards.
Job Description
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
Take your career to the next level and lead challenging full-service clinical research projects in phase II and III, managing the full scope of responsibilities and getting hands-on involvement in every aspect of the study.
Your responsibilities will include:
- Managing small (<5 countries and/or limited services) projects under direct or general supervision, with primary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget
- Performing regional lead’s or project co-manager’s role in complex international projects/programs with the secondary responsibility for the production of project deliverables in conformance with the predefined quality standards, on time and on budget.
- Adhering to and promoting principles of delivery and service in dealing with PSI customers.
- Leading project teams
- Training, mentoring, and coaching Lead CRAs, Senior CRAs, CRAs, Project Coordination Associates (PCAs) and Site Management Associates (SMAs)
- Participating in feasibility research
- Supporting business development tasks such as proposals, client presentations, bid defense meetings, etc.
- Implementing company standard practices and complying with intradepartmental procedures
Qualifications
- Bachelor's degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities. Equivalency is defined as a minimum 5 years of experience gained in pharmaceutical/healthcare industry and clinical research.
- At least 5-year industry experience in clinical research
- At least 2-year recent clinical research experience in the capacity of project manager/equivalent (e.g. Clinical Trial Manager, Clinical Study Team Lead, etc.).
- Regional clinical project management experience, including management of all project services from startup to closure
- Therapeutic experience in Oncology, Gastroenterology, and/or Radiopharmaceuticals is a plus
- Excellent communication skills, both written and verbal, with the ability to build strong internal and external stakeholder relationships
Additional Information
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.
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
Company size
1,001-5,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Zug
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
Company size
1,001-5,000 employees
Industry
Pharmaceutical Manufacturing
Org type
Privately Held
Headquarters
Zug