Jennifer Kuhl
Big Bend
Summary
Dynamic clinical research leader with extensive experience at Allergy, Asthma & Sinus Center, S.C., excelling in managing over 150 trials. Proven ability to implement innovative technologies and enhance team productivity. Strong knowledge of regulations combined with excellent organizational skills ensures high-quality outcomes in respiratory trials. Committed to ethical research practices and team collaboration.
Overview
26
26
years of professional experience
1
1
Certification
Work History
Director of Clinical Research
Allergy, Asthma & Sinus Center, S.C.
09.2009 - Current
- Responsible for the day-to-day management and coordination of clinical trials, ensuring they are conducted ethically and accordance with ICH GCPs.
- Oversight of clinical research coordinators, regulatory coordinator and recruitment coordinator.
- Selection of appropriate Sponsor-initiated clinical trials and oversight from site selection to close out.
- Negotiate contract and budget and budget reconciliation.
- Creation and editing of site standard operating procedures (SOPs) and responsible for ensuring all staff are adequately trained and follow SOPs.
- Implemented new electronic technology to streamline daily processes such as e-Regulatory, e-Source and e-Consent without compromising quality or safety standards.
Certified Clinical Research Coordinator
Allergy, Asthma & Sinus Center, S.C.
05.2006 - Current
- Coordinate and manage clinical trials in compliance with applicable regulations and standard operating procedures (SOPs)
- Ensure the timely completion of study tasks and met project timelines
- Screen, recruit, and consent participants for clinical trials and maintain their study records
- Conduct and document study visits and procedures, including informed consent, vital signs, detailed medical history, ECGs, PFTs, and medication review
- Collaborate with investigators, sponsors, and other team members to ensure the study's success
- Prepare and maintain regulatory documents and submissions, such as IRB applications, progress reports, and safety reports
- Collect and enter study data into electronic data systems (EDC, ePROs)
- Train and mentor new clinical research staff members
Operation and Orientation Supervisor
UPS
08.1999 - 09.2006
- Oversaw daily operations of the department, ensuring smooth workflow and timely completion of tasks.
- Applied strong leadership talents and problem-solving skills to maintain team efficiency and organize workflows.
- Increased team productivity by implementing efficient workflows and setting clear expectations for staff members.
- Responsible for holding employees accountable for safety, attendance and quality service.
Education
Kinesiology
University of Wisconsin-Milwaukee
Milwaukee05-2004
Skills
- Strong knowledge of clinical research regulations, guidelines, and processes
- Proficient in Microsoft Office Suite and electronic data capture (EDC) systems
- Excellent organizational, communication, and interpersonal skills
- Ability to work independently and collaboratively in a team environment
- Detail-oriented and committed to producing high-quality work
- Extensive experience in respiratory trials
Accomplishments
Strengthened the Allergy, Asthma & Sinus Center clinical research department over the past 19 years from 1 employee to 6, while providing quality data and meeting enrollment goals.
Affiliations
Association of Clinical Research Professionals (ACRP)
Society for Clinical Research Sites (SCRS)
Certification
- Certified Clinical Research Coordinator (CCRC), Association of Clinical Research Professionals - 2008-current
- IATA, Saf-T-Pak, 2006-current
- GCP, CITI Program, 2006-current
Languages
English
Timeline
Director of Clinical Research
Allergy, Asthma & Sinus Center, S.C.
09.2009 - Current
Certified Clinical Research Coordinator
Allergy, Asthma & Sinus Center, S.C.
05.2006 - Current
Operation and Orientation Supervisor
UPS
08.1999 - 09.2006
Kinesiology
University of Wisconsin-Milwaukee
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