MCRA, an IQVIA business, is a leading medical device advisory firm and clinical research organization (CRO). MCRA's value contribution rests within its industry experience at integrating five business value creators—regulatory, clinical research, reimbursement, healthcare compliance, and quality assurance—to provide a dynamic, market-leading effort from concept to commercialization. MCRA's integrated application of these key value-creating functions provides unparalleled expertise for its clients. MCRA has offices in Washington, DC, Manchester, CT, New York, NY, and a global presence in Japan and Europe and serves more than 1500 clients globally. Its core focus areas of therapeutic experience include orthopedics, spine, cardiovascular, neurology, digital health, diagnostic imaging, wound care, dental, general healthcare, robotics, and in vitro diagnostic (IVD) devices.
MCRA is seeking a dynamic proposal professional who will be responsible for supporting the coordination and content response development of request for proposals (RFP) across the organization’s core business units. The position will primarily be responsible for proposal development and providing general administrative support to the proposal team, including support with file maintenance, and tracking.
Responsibilities
- Review RFPs and develop proposals-based client requests.
- Work with internal departments to maintain list of active proposals.
- Coordinate meetings with proposals team and internal departments.
- Create proposal budgets.
- Gather and review information from requests for proposals to incorporate into various proposal formats.
- Develop clinical trial budgets to ensure all requested and required information in the RFP is provided in the final client deliverable.
- Communicate proposal development processes to internal departments and teams.
- Ensure timely communication and completion of tasks across all departments.
- Review and submit completed proposals.
- Contribute to the maintenance of databases and the preparation of reports.
- Responsible for tracking communication with clients, budgets, and all other documents as requested.
- Create response templates and other documents as needed.
- Conduct research as requested by supervisors.
- Ensure all work products comply fully with standards, policies, and mission of MCRA, an IQVIA business.
Qualifications
- Education: Bachelor’s degree is required.
- Experience: Minimum 2 years of experience in a professional environment.
- One or more years of experience in clinical research at a CRO, medical device company, or similar is required.
- Advanced proficiency in Microsoft Excel, preferred.
- Ability to read, write, speak and understand English required.
- Ensure work meets client and company standards.
NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as to meet the ongoing needs of the organization.
MCRA, an IQVIA business, is an equal opportunity/Affirmative Action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.
Top Skills
What We Do
MCRA is a highly specialized, independently operated consulting firm and Clinical Research Organization (CRO) serving the worldwide medical device industry. MCRA is a group of leading strategists committed to integrating regulatory, clinical, reimbursement, quality assurance, and healthcare compliance strategies to facilitate successful value creation for our clients. Founded in 2003, the firm provides “first-in-class” service to its clients through its superior knowledge base, global surgeon relationships, and deeply experienced management team. MCRA places particular emphasis on its expertise working with companies in all stages of development and throughout the technology life cycle by ushering technologies from the conceptual pre-clinical stage to market approval.
Our mission is to be the most experienced musculoskeletal strategic advisory team to guide our clients' products through the regulatory, clinical research, reimbursement, compliance and quality assurance processes quickly and successfully, to create maximum value for their shareholders.
Our vision is to be the market leading medical device advisory firm. Recognized as the market leading provider of regulatory, reimbursement, clinical research, compliance, quality assurance, and hospital services, MCRA’s vision is to provide the same leading quality of services throughout the medical device industry.
