Research Coordinator-Anesthesia
About The Position
This role is responsible for developing a sustainable research infrastructure and personnel team in collaboration with the Director of Pain Medicine, Vice Chair of Research, and Chair of Anesthesia. The position involves aiding in IRB protocol development and submissions, recruiting and consenting patients from various Endeavor sites, and maintaining organized study records. The Research Coordinator will also assist in recruiting personnel, performing data entry and quality control, and handling regulatory tasks for clinical trial startup and closeout. This role serves as a connection to CRAs and PIs, trains other team members, and develops into a clinical trials subject matter expert. Responsibilities include analyzing and summarizing data, presenting findings, performing scientific literature searches, and participating in abstract, poster, and manuscript preparation.
Requirements
- High school diploma required
- Experience leading projects and teams
- A commitment to producing high-quality work
- Basic understanding of the research process
- Strong communication, interpersonal and organizational skills
- Ability to work both independently and in teams
- Ability and willingness to learn new techniques to deploy on current and future studies
Nice To Haves
- Bachelor’s degree preferred
- SOCRA or ACRP preferred, but not required.
- Previous clinical or health services research experience
- Clinical Trials experience
- experience in perioperative and pain management clinical research suggested.
Responsibilities
- Work with the Director of Pain Medicine, Vice Chair of Research and Chair of Anesthesia to develop a sustainable research infrastructure and personnel team.
- Aid in IRB protocol development, submissions, inclusive of HIT review requests.
- Recruit and consent patients from a variety of Endeavor sites.
- Maintain organized and detailed study records.
- Aid in recruiting other personnel that are required to build a sustainable program.
- Perform data entry, quality control, and cleaning tasks in order to prepare data for statistical analyses.
- Regulatory work for clinical trial startup and closeout.
- Serve as connection to CRAs and PI.
- Train other team members.
- Develop into a clinical trials subject matter expert.
- Analyze and summarize data and present it in a variety of ways including power point presentations.
- Perform scientific literature searches as required.
- Participate in abstract, poster and manuscript preparation.
Benefits
- Premium pay such as shift, on call, holiday and more based on an employee’s job (For eligible positions)
- Incentive pay for select positions
- Opportunity for annual increases based on performance
- Career Pathways to Promote Professional Growth and Development
- Various Medical, Dental, Pet and Vision options
- Tuition Reimbursement
- Free Parking
- Wellness Program
- Savings Plan
- Health Savings Account Options
- Retirement Options with Company Match
- Paid Time Off and Holiday Pay
- Community Involvement Opportunities
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
