Company 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 3000 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.

Job Description

We’re searching for a knowledgeable, team-oriented, and proactive leader to supervise the clinical aspects of full-service global projects in China. As a Lead CRA at PSI, you will work on the frontline of communication with project stakeholders, ensuring the successful conduct of clinical trials in a variety of therapeutic indications. You will maintain the highest quality standards in the industry, while performing and supervising study start-up, clinical monitoring and site management activities on the country/regional level.

Responsibilities：

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.

QualificationsRelevant 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 5 years’ site monitoring experience with participation in global clinical projects as a Lead Monitor. -Must have prior experience monitoring or managing sites and CRAs in China with knowledge of China regulatory guidelines and practices.-Experience with all types of monitoring visits in Phases I-III.-Strong experience in Oncology 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

Additional Information

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!