Clinical Research Coordinator
7 months ago
**Schedule**
Monday to Friday, 8:30am-4:30pm
**Education Level**
Masters degree in a relevant field of study
**Career Level**
Requires 5 years of relevant experience
Should the successful applicant be a Unifor Unit 1 bargaining unit member, who meets the eligibility conditions of Article 19.02 of the Unifor Unit 1 Collective Agreement, then the Limited Term Assignment will be defined as a Career Growth Opportunity in accordance with Article 19 of the Unifor Local 5555 Unit 1 Collective Agreement.
Clinical Research Coordinator (III)
JD0572
Reporting to Dr. Margaret McKinnon, the **Clinical Research Coordinator (III) **will be responsible for working with the trauma and recovery research team on the Clinical Interventions Projects. Research is focused on developing novel interventions for individuals with post traumatic stress disorder (PTSD) and occupational stress injuries.
This role is for a duration of 12 months plus one day with the Department of Psychiatry.
**Job Summary**:
Responsible for assessing, planning, implementing, and evaluating protocol procedures and managing the daily operations of clinical research projects ensuring that all aspects of the project protocol are adhered to. Applies specialized knowledge to initiate, implement, coordinate, and manage moderate to large clinical research projects.
**Key Responsibilities**:
- Monitor and coordinate multiple research projects in order to assess the need for and to implement strategies to ensure the conduct of quality research, the achievement of expected time lines and deliverables, and the efficient use of human and practical resources.
- Troubleshoot problems at all stages of project development and implementation and assist with modifying protocol or project procedures to address challenges.
- Participate with a team in the development and authoring of research protocols.
- Recruit patients and enlist agencies to refer patients.
- Review referrals and keep track of intakes from various referral sources.
- Develop an implementation plan for research projects.
- Design promotional strategies and related materials to encourage participation and support for research projects.
- Perform both quantitative and qualitative analyses.
- Provide advice on and conduct analyses of complex data sets.
- Interview patients to gather qualitative and quantitative data.
- Facilitate focus group sessions with project patients.
- Gain the cooperation of research partners and team members by acting as the first point of contact on a variety of research projects and liaising with project collaborators, stakeholders, and staff.
- Exchange technical and administrative information with colleagues and project participants.
- Coordinate and manage the collection, delivery, entry, verification, analysis, and reporting of data.
- Identify funding opportunities and coordinate the submission of research proposals.
- Oversee the design of databases, data collection forms, error checking methods, and related programs for collection, analysis, and reporting.
- Write sections of scientific papers, funding proposals, and abstracts. Develop estimates of time and resources for research projects.
- Use statistical software to analyze data and interpret results.
- Write data management and operations documentation for projects.
- Liaise between the clinic centre and remote clinic sites and personnel.
- Ensure that relevant research methodology is applied and all research material is handled in accordance with established protocols, policies, and procedures.
- Develop presentations and present information and training sessions to project personnel and patients.
- Present at meetings, seminars, and conferences.
- Keep project participants informed of project progress through regular reports and newsletters. Implement and maintain research project budgets. Create financial projections and make adjustments to research project budgets throughout the fiscal year.
- Exercise appropriate controls, monitor, and reconcile accounts.
- Conduct literature searches
.**Qualifications**:
Education: Masters degree in a relevant field of study
Experience: Requires 5 years of relevant experience
**Additional Information**:
Additional Experience or knowledge in the following is a requirement of this position:
- Knowledge of Good Clinical Practice, TCPS2-2022 and other ethics related certifications required
- Proficiency with MS Office required (Outlook, MS Word, Excel, PowerPoint)
- Strong written and oral communication skills are necessary. The ability to work collaboratively in a team setting and to effectively manage multiple studies and timelines is required.
- Strong problem solving, interpersonal, communication and organizational skills are required.
- Experience in qualitative/quantitative research, project management, and community-based research
**How To Apply**
**Employment Equity Statement**
McMaster University is located on the traditional territories of the Haudenosaunee an
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