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Research Manager

1 week ago

Markham, Ontario, Canada ViziRecruiter,LLC. Full time

**Job Summary:**

We are seeking a highly motivated and experienced Research Manager to join our team at ViziRecruiter, LLC. As a key member of our research department, you will be responsible for promoting sound research practices, engaging research partners, and facilitating funding opportunities.

Responsibilities:

  • IDentify, develop, and implement new studies.
  • Review existing quality, clinical, and administrative management tools, standards, guidelines, processes, and procedures that integrate clinical research.
  • Facilitate regulations and guidelines governing clinical research.
  • Develop and modify clinical research plans for future service requirements.
  • Collaborate with investigators in the development of single and multiple site study budgets.
  • Monitor and manage budgets on an ongoing basis.
  • Manage grant/foundation research funds, assist with recruitment for grant-funded positions.
  • Coordinate research contracts with appropriate institutional legal sign-off.
  • Provide supervision/guidance of assigned clinical research staff and volunteers as necessary.
  • Oversee education of research staff and REB members.
  • Build web-based access: intranet & internet for clinical research information, education tools, document submission, and facilitate knowledge translation.
  • Provide oversite support for research training compliance.
  • Create, manage, and oversee REB SOPs, clinical research guidance documents, and policies.
  • Attend various conferences, meetings, and workshops to represent OVH.

Requirements:

  • Masters degree in a related field (i.e., research, science, business).
  • Hold recognized certification in clinical research (e.g., ACRP or SOCRA).
  • Minimum 2-3 years of Research Ethics (REB) experience and 5 years' clinical research experience.
  • Minimum 2 years' management experience directly supervising staff.
  • Knowledge of the Tri-Council Policy Statement, the Canada Food and Drug Act, the ICH Good Clinical Practices, and other relevant provincial, national, and international regulations and current regulatory developments.
  • Experience managing study budgets and strong understanding of research accounting practices.
  • Experience working with legal partners with strong understanding of research contractual language and agreements.
  • Experience performing feasibility assessments, site selection visits, budget reviews, and negotiations with Sponsors.
  • Experience with audits and inspections.
  • Strong understanding of Clinical Trials Ontario and OCREB.
  • Strong knowledge of clinical research terminology.
  • Strong attention to detail.
  • Excellent written/verbal communication skills.
  • Exceptional organizational, time management, and problem-solving skills.
  • Self-motivated with an enthusiastic, positive attitude, and excellent multi-tasking ability.
  • Ability to work effectively both independently and in a collaborative fast-paced team environment.
  • Proficiency with Microsoft Office, including Excel, and the ability to learn other applications.
  • Exercises judgment and decision making, using established policies and procedures to resolve technical problems.
  • Demonstrated understanding of policies, procedures, and issues dealing with research integrity and the conduct of research.
  • Flexible with superior organization skills and the ability to work efficiently to prioritize multiple, competing tasks in a fast-paced and dynamic environment.
  • Ability to exercise sound judgment and discretion, make decisions, and take initiative while working with confidential patient information and responding to patient inquiries.
  • Familiarity with REDCap and creating metrics for reports.