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The Associate, Proposals at MCRA will coordinate and develop responses to requests for proposals (RFPs), support proposal development, maintain active proposal lists, create budgets, and ensure compliance with company standards. They will also communicate processes internally, track client communications, and conduct research to support proposal efforts.

The Clinical Data Manager will lead data management on assigned projects, ensuring compliance with GCP and GCDMP guidelines. Key responsibilities include developing data management plans, ensuring data integrity, serving as the primary contact for data management with clients, and maintaining EDC systems for clinical studies.

The Associate Data Manager supports Clinical Data Managers with clinical data management tasks. Responsibilities include data entry, query resolution, maintaining documentation, and analyzing datasets. Strong organizational skills and attention to detail are necessary, often working with limited oversight.

MCRA is gathering interested candidates for future job openings in various roles within their medical device advisory services and clinical research support. This entails integration of regulatory, clinical, reimbursement, healthcare compliance, and quality assurance expertise for clients.

The Research Associate in the RHEMA team will conduct research on reimbursement policies, develop expertise in healthcare reimbursement systems, prepare client deliverables using Microsoft Office, manage project budgets and timelines, and present findings to clients and colleagues.