Groom & Associates
To display this page you need a browser with JavaScript support.
Study Manager, Clinical Trials
Title: Project Manager, Clinical TrialsWork Location: Downtown, Montreal, QC (hybrid)Permanent Position, Full-timeJob Summary:Responsible for the overall management of the clinical study. Primary contact for all communications. Responsible for the setup, conduct, and closure of the study in relation to other departments.Responsibilities:Customer (internal and external) satisfaction: ensuring project success• Coordinating communication with all parties involved in the study.• Monitoring study reports and progress with other departments to adjust study communication accordingly.• Facilitating actions to be taken in all aspects (sponsor decisions, communication, bottleneck resolution).Project Management:• Handling standardized operations and delivering the project on time and with good quality.• Project management coordination: planning and implementation, tracking of deliverables, and budgeting.• Monitoring and reporting client complaints, bottlenecks, or scope changes in terms of risk analysis and impact.• Responsible for study specifications and documentation.Quality Assurance:• Adherence to the quality assurance system.• Supporting continuous improvement by appropriately reporting deviations and bottlenecks.• Maintaining KPIs and dashboard with the STM lead to track performance in studies.• Supporting client audits.Required Skills:• Minimum 3 years in clinical project management or CRA.• Understanding of the clinical research ecosystem and its challenges: Keeping up-to-date with the latest technologies and advancements in the field of clinical research.• Mastery of fundamental project management principles: In-depth understanding of project management principles. This includes planning, organizing, budgeting, risk management, resource management, and time management.• Knowledge of regulations: Understanding local and international regulations.• Knowledge of IT tools: Proficiency in project management, data collection, and statistical analysis tools is necessary to facilitate study management.Required Competencies:• Budget management: Ability to manage the project budget, monitoring expenses, forecasting costs, and ensuring resources are used efficiently.• Time management: Meeting project deadlines, data collection, and result analysis.• Team management and leadership: Supervising and motivating study stakeholders.• Data management: Ability to analyze data effectively and securely to ensure result integrity.• Ethics and integrity: Adherence to ethical principles of clinical research.• Risk management: Identifying, evaluating, and mitigating risks associated with the clinical study.• Problem-solving skills: Ability to quickly resolve issues and obstacles to ensure the smooth progress of the study.• Communication: Effective communication, presenting study results to stakeholders, and collaborating with other professionals.• Adaptability: Rapid adaptation to new circumstances is important.• Leadership: Guiding the team and inspiring confidence.• Stress management: Crucial for handling the pressure of complex clinical research projects.• Teamwork: Collaboration with a multidisciplinary team is essential.• Perseverance: Necessary for overcoming obstacles in clinical research.• Results orientation: Focused on achieving study objectives.• Honesty and transparency: Important in communication with the research team, stakeholders, and patients.
Votre partenaire en recrutement – Your recruitment partner www.groomassocies.com
© 2018 - 2019 Groom & Associates. All rights reserved.