Clinical Project Manager
Clinical Project Manager
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Salary Not Disclosed
1 Vacancy
Job Description
Position Summary:
The Clinical Project Manager (CPM) will oversee and coordinate clinical activities across multiple projects while managing timelines communication and deliverables. This role involves working closely with crossfunctional teams investigational sites and stakeholders to ensure projects are executed efficiently and in compliance with regulatory requirements. The CPM is also responsible for building site relationships maintaining progress and addressing any issues during the project life cycle.
Key Responsibilities:
Serve as the primary point of contact for clinical operations on assigned projects ensuring effective communication and coordination.
Manage timelines project deliverables and communication flow to maintain synergy across teams and units.
Develop implement and maintain project dashboards reports and data repositories.
Assist in the development of proposals budgets and contracts as required.
Provide daily coordination and supervision of scheduled and ongoing projects ensuring timelines and deliverables are met.
Prepare professional communications and design new projects for internal and external stakeholders.
Ensure compliance with SOPs regulatory requirements and customer expectations in all work products.
Collaborate with investigational sites to ensure timely data submission collections and shipping.
Conduct sitelevel training and support enrollment status updates and inventory management in databases.
Investigate and resolve data discrepancies reconcile data and implement GMP/GLP/ISO/safety regulations.
Maintain strong client relationships and push teams to meet deadlines while fostering a collaborative working environment.
Other duties as assigned.
Requirements
Requirements:
Bachelor s degree in Biology Information Technology or a related field.
3 years of general work experience with at least 2 years focused on project management or equivalent clinical research roles (e.g. Clinical Research Assistant CRC).
Experience with project management software (e.g. MS Project Smartsheet).
Proficiency in MS Word Excel and PowerPoint.
Strong communication organizational and multitasking skills.
Ability to work collaboratively in a team environment.
Fluency in English both written and verbal.
Reliable transportation and availability for extended hours as needed to meet business demands.
Preferred Qualifications:
3 years of combined project or data management experience in clinical trial services laboratory services or related fields.
Familiarity with immunology molecular biology or genetics terminology.
Experience creating project plans Gantt charts CRFs and clinical documents.
Project management certification (PMI PMP) or Certified Clinical Research Professional (CCRP) certification.
Familiarity with GLP GMP GCP CLIA and ISO regulatory guidelines.
Employment Type
Full Time
