Technical Project Planner for wastewater technology at KLARO, managing projects from planning to implementation while liaising with clients.
About the role
- Study Manager at Evolution Research Group managing clinical trial projects. Collaborating with clinical teams to ensure successful project conduct and timely deliverables.
Responsibilities
- Primary site contact for assigned clinical studies.
- Lead site clinical team in sponsor study startup and study conduct.
- Ensure effective study plans are in place and operational for each trial and work proactively with the Clinical Trial Team to set priorities in accordance with applicable study plans, company standard operational procedures (SOPs), ICH/GCP guidelines and regulatory requirements.
- Proactively manage site level operational aspects of their assigned clinical study and ensure the timely delivery of all requested study logs/spreadsheets to sponsors i.e., Enrollment logs, protocol deviation spreadsheet, AE spreadsheet etc.
- Review and approve site visit reports; ensure tracking, follow up and resolution of site issues have been completed in a timely manner.
- Ensure the quality of vendor deliverables, address quality issues with the appropriate team member/s and identify opportunities to improve training, execution, and quality control across the clinical team.
- Ensure all site level study documentation is filed in the TMF in accordance with company SOPs/all regulatory requirements and provide oversight to the clinical team regarding TMF filing, maintenance and archival procedures.
- Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.
Requirements
- Minimum of 2 years of experience in clinical research coordination and project management
- Managing project teams through excellent interpersonal communication skills; experience motivating a group to reach a common goal and working collaboratively.
- Planning and organizational skills are required.
- Must have a thorough knowledge of clinical research concepts, practices, FDA regulations and ICH. Guidelines regarding drug development phases, clinical research, and data management methods.
- Excellent verbal and written communication skills
Benefits
- medical and dental coverage
- a matching 401(k)
- paid time off to recharge
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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