Description
POSITION SUMMARY
The Clinical Evidence Specialist is a key member of the Clinical Affairs team and drives clinical evidence development, key opinion leader development, continuing education program development and other special projects.
This position develops, documents, and executes pre-market and post-market clinical evidence studies across Agiliti-manufactured product platforms / families.
PRIMARY OBJECTIVES AND RESPONSIBILITIES
Clinical Evidence Specialists are responsible for :
- Collaborating with customers to develop pre- and post-market clinical evidence on the clinical use of Agiliti-manufactured product and clinical outcomes, in the forms of posters, publications, and white papers
- Supports product development teams on issues relating to pre-market and post-market clinical evidence needs and studies
- Collaborating with the Commercial and Clinical team to identify and develop key opinion leaders that will present on clinical outcomes of product at customer and potential customer engagements
- Gathering and analyzing clinical data, including web analytics, statistics, and trends
- Provide consultative services, and act as a liaison with cross-functional work teams, key stakeholders, and subject matter experts
- Identify and collaborate with partner clinical research / outcomes sites
- Identify and develop customer references
QUALIFICATIONS
- Four-year degree required in medical, nursing, biological, physical, or engineering disciplines.
- Experience in creating conference posters, white papers, and publications, and jointly with clinical research sites
- Experience in gathering and interpreting qualitative and quantitative clinical outcomes data
- Experience in acute care hospital setting required; beds and support surfaces highly preferred
- Knowledge of regulatory requirements relative to clinical investigations in at least one of the following regions : U.
S. FDA regulations, the Medical Devices Directive, and ISO 14155 Clinical Investigations standard
- Experienced in searching medical literature and databases for clinical and technical information
- Ability to read, analyze, and interpret clinical literature, regulations, guidance documents, clinical and medical terminology, technical product information and complex documents.
- Effective written and verbal communication skills in the area of technical / clinical applications
- Working knowledge of statistics and their application to clinical studies.
- Ability to create and maintain strong customer relations
- Strong project management skills with the ability to work independently
- Proven experience working with multidisciplinary, cross-functional teams
- Exceptional written and oral communication skills, including the ability to effectively communicate with clinical, legal, R&D, quality, marketing, and sales audiences
- Self-motivated, self-directing, strong attention to detail and excellent time management skills
- Project management skills
- High level of flexibility, creativity, dependability, and professionalism
- Excellent presentation skills are essential
- Demonstrated computer skills preferably spreadsheets, word processing, internet research and other applicable software programs.
- Travel up to 75%
DISCLAIMER
This job description in no way states or implies that these are the only duties to be performed by the employee in this position.
It is not intended to give all details or a step-by-step account of the way each procedure or task is performed. The incumbent is expected to perform other duties necessary for the effective operation of the department and the company.
Primary Job Location :
Houston District
Additional Locations (if applicable) :
Baltimore District, Boston District, Cleveland District, Philadelphia District
Job Title :
Clinical Evidence Specialist
Company : Agiliti
Agiliti
Location City : Houston
Houston
Location State : Texas
Texas
Pay Range for All Remote Locations :
$85,726.90-$160,999.30