Job Description

 Monitors investigator sites with particular ability to manage complex studies

and/or challenging sites using 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).

 Supports Clinical Team Management, including or Clinical Manager of CRAs (CMCRA), to mentor, train and contribute to the development of junior CRAs. Assists

in project specific training for the clinical team where necessary. Identifies areas

for potential process improvements, share potential solutions & implement where

appropriate.

 Facilitates effective communication between investigative sites, the client

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

contacts

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). Performs QC

check of reports generated from CTMS system where required.

 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.

 Responds to company, client and applicable regulatory

requirements/audits/inspections.

 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.