Research Project Manager II at Hamilton Health Sciences

Hamilton, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

26 Jan, 26

Salary

0.0

Posted On

28 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Research Management, Clinical Trials, Data Collection, Budget Development, Team Leadership, Communication, Problem Solving, Risk Management, Study Protocols, Training Material Development, Stakeholder Coordination, Conflict Resolution, Study Committee Organization, ICH-GCP Guidelines, Research Methodology, Drug Development Processes

Industry

Hospitals and Health Care

Description

The Research Project Manager II is to lead a team in the central coordination of one or more multi-centre research studies and to act as the primary point of contact for internal departments and external stakeholders. Responsibilities include: Review and provide input into research study protocols; Develop and design materials to assist in conduct of study, including informed consent form templates, recruitment materials, manual of operations, training material; Liaise and coordinate with internal departments to ensure requirements and timelines are achieved as required; Support the Principal Investigator (PI) in the identification, development and organization of required study committees; Monitor study management plans throughout project; Control for risk identification, risk mitigation and issue resolution for the research study; Prepare and present reports, abstracts, posters, and academic manuscripts;. Ongoing management of data collection and validation systems, processes, and associated documentation; Development of research study budgets; Negotiate budgets with vendors, sites and national leaders; Provide leadership, coaching, training and mentorship to study team members; manage the performance and workload for study team members; Develop targets and timelines for deliverables, anticipates potential delays and proactively develop strategies to achieve a positive outcome; Represents the research study team at program and other organizational meetings; and Negotiate and resolve conflicts among study team members. 1. Minimum 5 years’ experience in multi-centre research studies and the management of large clinical research datasets. 2. Undergraduate degree in sciences or health science and a clinical research certification (CCRP, ACRP or other post-graduate certification in clinical research). 3. Minimum 3 years supervisory experience. 4. Excellent communication, problem solving skills and ability to work flexible hours. 5. Knowledge of ICH-GCP Guidelines and international research requirements. 6. Broad knowledge of research methodology, clinical trials and drug development processes.

Responsibilities

The Research Project Manager II leads a team in coordinating multi-centre research studies and serves as the primary contact for internal and external stakeholders. Responsibilities include developing study materials, monitoring project plans, managing data collection, and providing mentorship to team members.