Qualifications MUST have a minimum of 7 years of experience in clinical trials in a CRO environment MUST have 2 years of direct Project Management or equivalent experience Hybrid Schedule 3 days work from home 2 days in office Hybrid Clinical Project Manager Plan and manage day-to-day operational aspects of one or more assigned programs/projects or tasks, including the following, as required: planning/timelines, budgeting, resourcing, and vendor management/interfacing; Identify and proactively work to remove obstacles, mitigate risks, and escalates issues; both internally and to the client (Contracting Officers Representative (COR), or designee(s)), as needed Interface with clients and program/project staff; ensure provision of meeting agendas and summary documentation, as well as detailed information required for internal and client meetings Prepare and/or review full or sections for monthly, quarterly, and annual reports; may present at internal and/or scientific meetings Ensure documentation of processes and workflows are being followed and occurring within projected timelines and determine course of action to prevent and remediate delays. Identify gaps and propose solutions to improve efficiency and quality of deliverables Represent clinical-trial related operations at study team meetings, participate in collaborative efforts and play an important cross-functional role Perform duties within established SOPs and in accordance with Good Clinical Practice (GCP); Ensure project quality and compliance with FDA regulations and ICH (R2) guideline, and with NIH policies or other sponsor-specific requirements Provide oversight and mentorship to staff in the delivery of quality work and performance metrics, as per task order and/or project deliverables Expect to include line management responsibility and staff hiring activities Support and comply with the company's Quality Management System policies and procedures; Drives innovative project and company performance improvement solutions, including corrective and preventive (CAPA) actions, as needed Perform risk-based quality content reviews and monitor internal/external KPIs, as required by the client Contributes to Corporate Initiati ves, e.g., SOP development and proposals for government and commercial clients About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.