*Terms and Conditions apply
JOB OVERVIEW: Responsible for remote site monitoring activities and site management of Phase II-IV clinical research studies to ensure that sites are conducting the studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Maintains effective communication with sites, establishing solid relationships with Investigators and all other site staff.
The Senior CRA will assist in monitoring the progress of clinical studies remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, Food and Drug Administration (FDA) Regulations, Good Clinical Practice (GCP), and company standard operating policies and procedures.
QUALIFICATIONS:
Clinical Research Associate II / Sr. Clinical Research AssociateMust have minimum of Bachelor’s degree in a health or science related field.Preferably graduate of Pharmacist or PHRN.Required experience should be highlighted in CV for the studies conducted (e.g vaccine, oncology related)Must be willing to start first week of MayKnowledge of clinical research process and medicalGood organizational and problem-solvingShift: Fixed night shift (Temporary Work from Home)*Site: Manila