Description

 

Clinical Project Manager (RH2017-16)

Under the guidance and supervision of the Manager of the Central Laboratory and in collaboration with the Clinical Project team, the Clinical Project Manager is responsible of supporting the team in the development, design, management and coordination of scenarios and strategies which will help achieving the objectives of each of the clinical studies under his responsibility.

Tasks and Responsibilities

  • Understands the objectives and deadlines for all assigned clinical studies under his responsibility.
  • Coordinate the different steps and activities related to the assigned projects, including: allocating activities to the different units and setting up follow-up procedures (tasks, budget, and deadlines).
  • Ensure the studies’ management, communications with clinical sites and internal communications are organized and standardized according to current procedures and SOPs.
  • Supervise the maintenance of the work plan and follow-up tools that allow all people involved in each study to monitor the activities and expected result.
  • Coordinate the capture of information, and the preparation/update of the study material (forms, reports, tables, memos) that is provided to the client including text revisions & translations, formatting, printing and assembling.
  • Prepare, write and analyze the different reports and protocols that are assigned to him throughout the project, and ensure compliance to CIRION’s quality standards.
  • Coordinate meetings and activities related to his assigned clinical projects. 
  • Prepare memos and related study documents in order to optimize the communication of activities and ensure the coordination and integration of all people involved. Setup and update study files, summaries, reports and budgets.
  • Respond to client requests for information in a timely manner, and provide the appropriate follow-ups.
  • Assist in managing assigned study start-ups, maintenance and closures (data entry, interactions with clinical sites, quality control, documentation maintenance, filing, etc.)
  • Manage the multiple client requests for proposals and prioritize in order to meet business objectives and deadlines.
  • Prepare and review his assigned proposals, work orders and change orders.
  • Organize and file the central laboratory information according to current procedures.
  • Represent CIRION in investigators meetings or other events that might include traveling abroad.
     

Qualifications

  • B.Sc. or M.Sc. in science, in a related field.
  • A minimum of 2 years of relevant management experience in clinical research project in a pharmaceutical environment or contract research organization (CRO). 
  • Excellent knowledge of GCP (Good Clinical Practice) and GLP (Good Laboratory Practice) standards. 
  • Written and verbal communication skills in French and English.
  • Knowledge of Microsoft Office softwares, specifically Word and Excel. 
  • Excellent organization, project management, client service and interpersonal communication skills.
  • Attention to details and analysis abilities.
  • Ability to work in collaboration with other team members.
  • Flexibility to work on multiple projects at the same time, and to meet the planned deadlines.

 

CIRION is an equal opportunity employer. Only those applicants selected for an interview will be contacted.

Privacy policy

Apply
 

© 2016 CIRION BioPharma Research Inc. All rights reserved.  Legal notice  Privacy Policy