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Senior Clinical Research Associate - CNS/Cardiovascular
Job in
Pembroke Pines, Broward County, Florida, 33028, USA
Listed on 2026-07-08
Listing for:
Piper Companies
Full Time
position Listed on 2026-07-08
Job specializations:
-
Research/Development
Clinical Research
Job Description & How to Apply Below
Piper Companies is seeking an experienced Senior Clinical Research Associate (CRA) to support CNS and Cardiovascular clinical studies in a dynamic, sponsor‑facing environment. This role will be responsible for overseeing site performance, ensuring regulatory compliance, and driving successful trial execution through strong site relationships and hands‑on monitoring activities. This is a full time opportunity that requires regional travel and can be located anywhere in the U.S.
Responsibilities for the Senior Clinical Research Associate include:- Independently monitoring Phase II–III CNS and Cardiovascular clinical trials to ensure compliance with study protocols, ICH‑GCP guidelines, and regulatory requirements.
- Conducting site initiation, routine monitoring, and closeout visits while maintaining high‑quality oversight of investigative sites.
- Performing source data review (SDR), source data verification (SDV), and case report form (CRF) review to ensure accurate and inspection‑ready study data.
- Building strong partnerships with investigative sites to support enrollment goals, protocol adherence, and overall study success.
- Collaborating directly with sponsors, study teams, and site personnel while providing regular updates on site performance and trial progress.
- 1+ years of Clinical Research Associate experience, including significant experience independently monitoring CNS and/or Cardiovascular clinical trials.
- Strong knowledge of ICH‑GCP guidelines, FDA regulations, clinical trial operations, and site management best practices.
- Experience supporting Phase II and Phase III studies with responsibility for site oversight, monitoring, and issue resolution.
- Proven ability to conduct site initiation, interim monitoring, and closeout visits independently.
- Strong sponsor‑facing communication skills and experience working directly with biotechnology or pharmaceutical clients.
- Ability to manage multiple investigative sites, prioritize competing demands, and work effectively with minimal supervision.
- Must be located within reasonable distance of a major airport and willing to travel regionally as required.
- Salary range: $100,000 - $115,000.
- Comprehensive benefits package including Medical, Dental, Vision, 401k, PTO, holidays, and sick leave as required by law.
This job is open for applications on 7/1/2026 and will remain open for at least 30 days from the posting date.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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