Lead Clinical Research Associate

Role Summary

Coordinates investigator/ site feasibility and identification process, as well as study startup.

Monitors project timelines and patient enrollment, implements respective corrective and preventive measures.

Reviews monitoring visit reports for all visit types and ensures reporting compliance of the Monitors in the region.

Manages Monitors in the query resolution process, including Central Monitoring observations.

Coordinates safety information flow and protocol/process deviation reporting.

Performs clinical supplies management with vendors on a country and regional level.

Ensures study-specific and corporate tracking systems are updated in a timely manner.

Acts as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager.

Coordinates planning of supervised monitoring visits and conducts the visits.

Manages the project team in site contracting and payments.

Leads project team calls on a country level as well as provides status updates and reports to Regional Lead/ Project Manager.

Ensures ongoing evaluation of data integrity and compliance at a country/regional level.

Conducts site audit preparation visits, may participate in site audits, and coordinates resolution of site audit findings on a country/regional level.

Oversees project team in CAPA development and implementation.

Coordinates project team in process deviations review, management and reporting.

Conducts initial training and authorization monitoring visits for Monitors and acts as a mentor for newly promoted Lead CRAs.

Provides project-specific training and prepares training materials for the project team under supervision of a Project Manager and Regional Project Lead.

Delivers trainings and presentations at Investigator Meetings.

Prepares, conducts and reports site selection, initiation, routine monitoring and closeout visits.

Ensures that subject recruitment targets and project timelines are properly defined, communicated, recorded, and met at site level.

Ensures accurate and timely information flow with trial sites on Adverse Events and protocol/process deviations.

Supervises source data verification and follows up on data queries at site level in the country/region; reviews and manages study risks on a site level.

Ensures proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and clinical study supplies on a country/region level.

Reviews essential study documents and supervises reconciliation of study Investigator Site File (ISF) / TMF at site level and country/region level.

Ensures data integrity and compliance at a site level.

Supervises Site Management Associates in the flow of documents and laboratory supplies between the site and the Central/ Regional Lab/ Central Reviewer.

Conducts project-specific training of site Investigators.

Supports preparation of draft regulatory and ethics committee submission packages.

Relevant educational background, such as MD, MPharm, RN or College/University degree in Life Sciences or an equivalent combination of education, training and experience.

Minimum of 4 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor or equivalent qualification level.

Must have prior experience monitoring or managing sites and CRAs with knowledge of US and Canadian regulatory guidelines and practices.

Experience with all types of monitoring visits in Phases I-III.

Strong experience in Oncology preferred.

Experience in CAR-T Therapy or other types of Cell Therapy, Gene Therapy, Radiation Therapy or Radiopharmaceuticals, or Nuclear Medicine is preferred.

Strong experience in GI (Chron's, Ulcerative Colitis, IBS) preferred.

Full working proficiency in English.

Proficiency in MS Office applications.

Ability to plan, multitask and work in a dynamic team environment.

Excellent Communication, collaboration, and problem-solving skills.

Ability to travel up to 65% (depending on project needs).

Valid driver’s license (if applicable).

Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapid growing company that puts its people first.

PSI is a leading Contract Research Organization with more 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.

About the Company

Why Join PSI?

At PSI, we believe exceptional people deserve an exceptional workplace.

When you join PSI, you'll benefit from

A stable, privately held CRO that has never undergone a merger or acquisition and has never experienced company-wide layoffs.

A unique leadership-focused CRA role with minimal travel and little to no routine site assignments.

Opportunities to mentor other CRAs and expand your leadership skills.

A collaborative, people-first culture where employees are genuinely supported.

Career development opportunities across a growing global organization.

The chance to contribute to innovative clinical research that improves patients' lives.

We are the company that cares - for our staff, our clients, our partners, and the quality of the work we do.

Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with more than 3,000 employees dedicated to advancing medical science and bringing new therapies to patients worldwide.

In an industry shaped by mergers, acquisitions, and restructures, PSI stands apart. We have remained privately held, have never undergone a merger or acquisition, and have never experienced company-wide layoffs. Our long-term stability allows us to invest in our people, foster meaningful careers, and build lasting partnerships with our clients.

If you're looking for a collaborative organization where you can continue to grow while making a meaningful impact, PSI is the right place for you.