Dharmender Singh

Scientific Study Associate @Altasciences

Laval, QC, CA

Autonomously and effectively facilitates the organization of study-related required support, including the coordination for both non-GLP studies and GLP studies from study initiation to finalization, via communications with internal departments and external clients, with continued attention to detail and consistency. The Study Director will be consulted with, as necessary, and duly copied/kept informed of all exchanges. • Consults independently with the Sponsor, peers, and other key individuals during protocol development to optimize the protocol design and is responsible for the preparation of protocols and/or amendments/amended protocols. Assures the current copies of approved protocol and/or amendments/amended protocols are available to all study personnel and Sponsors.• Responds, or accurately investigates for the Study Director’s response, to inquiries from internal and external study personnel regarding scientific and/or logistical (scheduling) aspects of the study.• Schedules and/or helps conduct protocol review meetings with Study Director guidance.• Assures schedule changes are captured and communicated as a result of protocol amendments/amended protocols, as necessary.• Drafts and edits project review forms.• Involved with planning and hosting of client visits.• Responsible for review of the raw data throughout the life of a study for clerical/technical errors, thoroughness and consistency, and adherence to SOPs and protocol specifications, and compliance with Good Laboratory Practices (GLPs), as appropriate. Assures coordination for any correction of raw data with appropriate staff. Assures any deviation or unforeseen circumstance that may affect the quality and integrity of the study was reported to the Study Director and addressed in a timely manner.

McGill University

Master's Degree

Bangalore University

Bachelor's degree

Rajiv Gandhi University of Health Sciences

Master's Degree