2 Manager of Scientific Evidence and Clinical Science Jobs in Gainesville, FL
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Manager of Scientific Evidence and Clinical Science
$94k-116k (estimate)
Full Time | Medical Technology
4 Days Ago
Exactech is Hiring a Manager of Scientific Evidence and Clinical Science Near Gainesville, FL
Department: Clinical Affairs
Employment Type: Permanent - Full Time
Location: US (Remote)
Reporting To: Director of Clinical Affairs
DescriptionThis position is responsible for facilitating the strategic planning and coordination of scientific evidence programs, leading the Clinical Science team, and ensuring high-quality medical writing and research services. The role manages and implements scientific evidence projects, developing cross-functional project teams, and maintaining strong relationships with various stakeholders.
Key Responsibilities
Employment Type: Permanent - Full Time
Location: US (Remote)
Reporting To: Director of Clinical Affairs
DescriptionThis position is responsible for facilitating the strategic planning and coordination of scientific evidence programs, leading the Clinical Science team, and ensuring high-quality medical writing and research services. The role manages and implements scientific evidence projects, developing cross-functional project teams, and maintaining strong relationships with various stakeholders.
Key Responsibilities
- Project Management and Implementation: Oversee the management and implementation of assigned scientific evidence projects. This includes leveraging and expanding experience for future project assignments and developing strategies that align with the company's goals.
- Collaboration with Stakeholders: Collaborate with Business Unit (BU) stakeholders to identify scientific claims for Exactech products early in the New Product Development (NPD) process. Act as the liaison and primary point of contact for all Clinical Science related issues across Exactech's global businesses.
- Leadership in Cross-Functional Teams: Lead specified BU cross-functional project teams in planning and executing pre-clinical and clinical studies. These studies should align with scientific claims and include strategies for preclinical study, clinical research, publication, and marketing communication.
- Scientific Evidence Platform Development: Develop scientific evidence platform strategies to be leveraged across BUs, such as Advanced Surgical Technologies.
- Relationship Building and Team Coordination: Establish, develop, and maintain strong working relationships with cross-functional project team members. Coordinate and supervise the activities of direct reports in the Clinical Science team.
- Engagement of Key Investigators: Facilitate early engagement of key surgeon investigators in research strategies.
- Scientific Publications: Drive the preparation and submission of scientific publications (white papers, abstracts, manuscripts) aligned with claims strategies. Manage publication submission timing to align with key annual scientific meetings/conferences.
- Clinical Science Management: Manage Clinical Science deliverables in collaboration with Regulatory, Quality, Engineering, and business leaders. Educate and mentor team members on medical writing and research best practices.
- Regulatory Compliance and Reporting: Prepare clinical evaluation reports for regulatory submissions, perform data analysis of clinical outcomes, and conduct literature reviews. Ensure compliance with FDA and international standards, including Design Control and Risk Management processes.
- Risk Management and Quality Assurance: Support risk/benefit analyses conducted by Engineering. Participate in complaint handling, corrective and preventive action, and internal quality audit processes. Provide knowledge and support to operate within company and regulatory guidelines.
- Project and Process Compliance: Independently manage multiple medium to large-scale writing/research projects. Ensure that company procedures, processes, and documentation meet required guidelines for maintaining FDA compliance and ISO/EC/CMDR certification.
- Internal Collaboration and Support: Work collaboratively with other functional areas to feed back the analysis of post-market information into Risk Management and the Design and Development process. Assist and support other employees, teams, and sales personnel as necessary.
- Company Values and Standards: Uphold and practice Exactech's values. Apply the Quality System and relevant Federal and International standards effectively.
- People leadership: Follow the Exactech leadership model, and lead the Scientific Evidence and Clinical Science team.
- Bachelor's Degree in a related field from an accredited institution required; Master's Degree preferred
- Five (5) years of experience in medical writing or similar field, with three (3) years supervisory experience
- Medical/Technical writing skills required
- Experience in systematic literature review required
- Experience in medical devices preferred
- Experience developing and documenting State of the Art reviews for medical products preferred
- Experience in project and team management
- Detail oriented and strong organizational skills
- Strong interpersonal communication skills
- Strong technical writing and written communication skills
- Working knowledge of Windows based office productivity tools including word processor and spreadsheet
Job Summary
JOB TYPE
Full Time
INDUSTRY
Medical Technology
SALARY
$94k-116k (estimate)
POST DATE
07/03/2024
EXPIRATION DATE
07/28/2024
WEBSITE
exac.com
HEADQUARTERS
GAINESVILLE, FL
SIZE
500 - 1,000
FOUNDED
1985
TYPE
Private
CEO
DARIN JOHNSON
REVENUE
$200M - $500M
INDUSTRY
Medical Technology
Related Companies
About Exactech
Exactech is a medical device company that designs, develops and produces bone and joint restoration products for orthopedic surgical procedures.
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