Axogeniscommittedto building and maintaining a strong andgratifyingcompany culture that fosters a work-life balance and professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process. Most benefits are effective on day one!
Axogenis the leadingcompany revolutionizing thescience of nerve repair.We arepassionate about helping to restore function and quality of life to patients with physical damage or discontinuity to peripheral nerves.
Contributetopositively impactinglives whileworkingfor a company that respects, recognizes, andvalues allteam members!
Axogenis an equal opportunity employer and does not discriminate against applicantson the basis ofrace, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status.
Axogen is hiring for a Clinical Development Scientist in Alachua or Tampa, FL!
Job Summary of the Clinical Development Scientist
The Clinical Development Scientist assists in the design, preparation, planning, analysis and interpretation of data for clinical projects and studies. This position ensures adherence to federal, state and AATB requirements and company and ethical standards.
Requirements of the Clinical Development Scientist
Minimum of BS in Life Sciences (MS or PhD preferred)
Minimum of 5 years' experience in clinical research
Strong sense of pride in your work product
Ability to take ownership in a project and drive it to completion
Passion for advancing scientific knowledge
Awareness of the impact of your contributions on your team, the company, collaborators, customers, patients, medical science and society
Responsibilities of the Clinical Development Scientist
The specific duties of the Clinical Development Scientist include but are not limited to:
Provide guidance on the design of clinical projects and studies to ensure appropriate data is collected to support commercial and healthcare economic initiatives
Assists with translation and interpretation of clinical data to assist with evidence generation activities such as manuscripts, abstracts, marketing collateral, and/or other internal scientific communications
Critically interpret relevant literature
Serve as a resource for clinical knowledge
Support investigator initiated clinical studies as assigned while ensuring adherence to institutional, local, federal, state, and company ethical standards
Serve as a content expert and liaison to the commercial teams related to clinical trial evidence for training and collateral material related to clinical programs
Develop or assist with the development of study-specific documents essential to appropriate implementation of clinical investigations
Participate in cross-functional efforts to improve clinical development initiatives
Assist with preparation and execution of Investigator meetings
Present information and data at investigator and team meetings
Assist with preparation of Ethics Committee submissions and notifications/submissions to federal and state regulatory authorities
Participate in project team meetings and provides clinical representation
Provide clinical support in working with the FDA
Follow company policies, procedures and standard operating procedures
Perform other duties as directed by the Supervisor