Prin CRA

 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 ( 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