Remote Clinical Operations Manager with branded pharmaceutical company! The candidate selected will be required to travel up to 30% in this position and must be located in EST.

　　Qualifications:

　　5 years’ experience- CRA Management and Oversight

　　Will be managing upwards of 8-10 CRAs. Will be involved in development and training of CRAs. Will run performance evaluations.

　　Line Manager for CRAs. Responsible for site assignments.

　　Co monitoring experience

　　Must come from a monitoring background

　　SOP development

　　Review trip reports

　　Coordinate with Project Manager

　　Meet with sites- including KOLs and Investigators.

　　Systems experience- IRT systems, EDC systems

　　Bachelor’s Degree in Life Sciences.

　　Seven years of previous experience in the Pharmaceutical Industry/Contract Research Organization.

　　Study plan writing experience.

　　Expertise in Clinical Trial Management Systems.

　　Experience with trial master file maintenance, auditing, and reconciliation, particularly on a site level.

　　Experience working in a multicultural environment with sensitivity to cultural distinctions

　　Responsibilities:

　　Lead and manage the clinical monitoring network in the United States.

　　Lead clinical operations in the United States in support of the clinical research trials.

　　Train and develop clinical research associates (CRAs).

　　Coordinate with the Clinical Project Managers in execution of monitoring and site management deliverables.

　　Ensure overall clinical operations study timelines are maintained.

　　Line management of CRAs.

　　Assess CRA performs and address issues promptly.

　　Assess and review investigational site metrics in collaboration with Clinical Project Manager(s) and Head of Clinical Operations, USA.

　　Serve as primary reviewer of monitoring visit trip reports.

　　Maintain and track investigational site monitoring metrics.

　　Function as a primary contact and partner for the Clinical Operations team.

　　Develop and foster relationships with key opinion leaders and investigators.

　　Ensure all clinical trial activities are carried out in compliance with Good Clinical Practices and applicable FDA regulations.

　　Establish and oversee day-to-day clinical monitoring performance, ensuring compliance with policies, procedures, and standard.

　　Provide input and feedback on the clinical strategic approach and the impact on the overall clinical development plan.

　　Collaborate with the Clinical Project team in review of clinical trial protocols.

　　Develop clinical monitoring plans and review additional study plans for the clinical trial, including but not limited to: Monitoring Plan, Safety Reporting Plan, Communication Plan, Risk Management Plan.

　　Learn medical and scientific details of the study indications.

　　Collaborate with internal partners and vendors for the management of clinical supply (investigational product) logistics, accountability, and destruction, drawing support from the monitoring team.

　　Perform additional duties assigned by line manager

　　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

　　Actalent is an equal opportunity employer.

　　About Actalent

　　Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.