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PSI CROPC

Regional Project Lead

PSI CRO is a global, full-service Contract Research Organization (CRO) founded in 1995, specializing in predictable patient enrollment and on-time delivery of clinical trials across various therapeutic areas. Headquartered in Switzerland, PSI operates in over 50 countries with a strong focus on quality and client satisfaction.

PSI CRO

Employee count: 1001-5000

United States only

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The Regional Project Lead is a senior level clinical trial manager who oversees, manages, and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.

  • Ensures planning, implementation, and management of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g., PSI QSDs or Sponsor QMS documents)
  • Acts as primary or secondary project management contact for the project team and PSI support services in designated countries
  • Performs study status review and progress reporting (if delegated by the Project Manager)
  • Collects and reports project status updates for designated regions, both internally and externally
  • Develops and updates project planning documents, essential study documents and project manuals/ instructions
  • Manages and reports on Key Performance Indicators (KPIs) for designated countries and clinical project team members
  • Ensures that the project timelines and subject enrollment targets are met in designated countries
  • Coordinates maintenance of study-specific and corporate tracking systems
  • Coordinates site contractual startup and budget negotiations
  • Establishes communication lines within the project team and supervises clinical project team members’ performance
  • Identifies, escalates and resolves resourcing and performance issues
  • Conducts and supervises therapeutic area training of the project team (if delegated by the Project Manager)
  • Prepares presentations and conducts training of Investigators
  • Ensures team compliance with project-specific training matrix
  • Performs field training of Monitors tailored to the project needs
  • Supervises preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits
  • Oversees investigator and site payments, as well as CRF data retrieval/ upload and monitoring and the query resolution process
  • Supervises project team preparation for study audits/ inspections and resolution of audit/ inspection findings
  • Coordinates conduct of supervised monitoring visits
  • Reviews site visit reports and ensures monitoring and reporting standards are met
  • Coordinates preparation of initial and follow-up Regulatory and Ethics Committee submissions and notifications
  • Oversees the safety information flow and participates in feasibility research
  • Reviews/approves project related expenses and timesheets (if delegated by the Project Manager)
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience is required
  • Prior experience in Clinical Research and on-site monitoring is required
  • Experience as a Study Manager/Clinical Trial Manager with the ability to supervise project activities as a Regional Lead or equivalent is required
  • Experience in Oncology is required
  • Experience in GI is preferred
  • Full working proficiency in English
  • Proficiency in MS Office applications, including MS Project
  • Communication, presentation and customer-service skills
  • Ability to negotiate and build relationships at all levels
  • Team building, leadership and organizational skills

Advance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! You will get hands-on involvement in every aspect of the study.

For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

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 2,800 driven, dedicated and passionate individuals. We work on the front-line 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.

About the job

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Posted on

Job type

Full Time

Experience level

Education

Bachelor degree

Experience accepted in place of education

Location requirements

Hiring timezones

United States +/- 0 hours

About PSI CRO

Learn more about PSI CRO and their company culture.

View company profile

We are a leading full-service global Contract Research Organization (CRO) with a key strength in predictable patient enrollment across multiple therapeutic areas. Since our founding in 1995 by Dr. Robert Reekie and Dr. Roger A. Smith, we've been dedicated to revolutionizing how clinical trials are conducted, focusing on delivering high-quality, cost-effective solutions worldwide. Our mission is to be the best CRO in the world as measured by our employees, clients, investigative sites, and vendors. This commitment is reflected in our exceptionally high repeat and referral business rates and minimal staff turnover.

Our global reach allows us to conduct clinical trials across multiple continents and in over 50 countries. We are known in the industry for our 'on-time project delivery,' a reputation we've built by investing substantial effort and medical expertise into performing quality feasibility assessments that provide accurate predictors of study timelines. In fact, over 90% of our studies finish on time or ahead of schedule. We specialize in planning and executing global pivotal registration clinical trials, particularly in complex areas like oncology, hematology, infectious diseases, gastroenterology, multiple sclerosis, and rare indications. We embrace innovation and technology, leveraging cutting-edge methodologies and data-driven insights to optimize trial design, streamline operations, and enhance patient engagement. Our robust quality management systems and adherence to the highest industry standards, including ISO 9001:2015 and ISO 27001:2013 certifications, underscore our dedication to excellence. We are proud of our contributions to advancing healthcare by helping bring life-saving therapies and treatments to market. We actively engage in research collaborations and knowledge sharing to contribute to scientific advancement.

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PSI CRO

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