Job Description

　　Monitors investigator sites with a risk-based monitoring approach, applies root

　　cause analysis (RCA), critical thinking and problem-solving skills to identify site

　　processes failure and corrective/preventive actions to bring the site into

　　compliance and decrease risks. Ensures data accuracy through SDR, SDV and

　　CRF review as applicable through on-site and remote monitoring activities.

　　Assess investigational product through physical inventory and records review.

　　Documents observations in reports and letters in a timely manner using

　　approved business writing standards. Escalates observed deficiencies and issues

　　to clinical management expeditiously and follow all issues through to resolution.

　　May need to maintain regular contact between monitoring visits with

　　investigative sites to confirm that the protocol is being followed, that previously

　　identified issues are being resolved and that the data is being recorded in a

　　timely manner. Conducts monitoring tasks in accordance with the approved

　　monitoring plan. Participates in the investigator payment process. Ensures a

　　shared responsibility with other project team members on issues/findings

　　resolution. Investigates and follows-up on findings as pplicable

　　 Provides updates on potential trends noted across multiple sites and discusses

　　potential strategies for their management to the Clinical Team Manager (CTM).

　　 Participates in investigator meetings as necessary. Identifies potential

　　investigators in collaboration with the client company to ensure the acceptability

　　of qualified investigative sites. Initiates clinical trial sites according to the

　　relevant procedures to ensure compliance with the protocol and regulatory and

　　ICH GCP obligations, making recommendations where warranted. Ensures trial

　　close out and retrieval of trial materials.

　　 Ensures that required essential documents are complete and in place, according

　　to ICH-GCP and applicable regulations. Conducts on-site file reviews as per

　　project specifications.

　　 Contributes to the project team by mentoring new members, assisting in

　　preparation of project publications/tools including informed consents, CRF

　　guidelines and monitoring plans, and sharing ideas/suggestions with team

　　members. Assists in project specific training for the clinical team where

　　necessary. Identifies areas for potential process improvements & share potential

　　solutions for improvements.

　　 Performs additional tasks as assigned by CTM or Clinical Manager of CRAs (CMCRA) (e.g. trip report review, newsletter creation, lead CRA team calls etc).

　　 Provides trial status tracking and progress update reports to the Clinical Team

　　Manager (CTM) as required. Ensures study systems are updated per agreed

　　study conventions (e.g. Clinical Trial Management System, CTMS). Perform QC

　　check of reports generated from CTMS system where required.

　　 Facilitates effective communication between investigative sites, the client

　　company and the PPD project team through written, oral and/or electronic

　　contacts.

　　 Responds to company, client and applicable regulatory

　　requirements/audits/inspections federal regulatory requirements/audits.

　　 Maintains & completes administrative tasks such as expense reports and

　　timesheets in a timely manner

　　Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.