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Senior Clinical Research Associate - CNS/Cardiovascular

  • Job type Posted on: Jul 17, 2026
  • Experience level Piper Companies
  • Employment type Orlando, Florida
  • Remote status Salary: $115,000 per year
  • Employment type Onsite
  • Salary Full-time

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Job Title :

Senior Clinical Research Associate - CNS/Cardiovascular

Job Type :

Full-time

Job Location :

Orlando Florida United States

Remote :

No

Jobcon Logo Job Description :

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. Qualifications for the Senior Clinical Research Associate include: 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. Compensation for the Senior Clinical Research Associate includes: 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-Ljbffr

Jobcon Logo Position Details

Posted:

Jul 17, 2026

Reference Number:

14660_9AFD6817D827DDB5C97A3110937AF60B

Employment:

Full-time

Salary:

Not Available

City:

Orlando

Job Origin:

APPCAST_CPC

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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. Qualifications for the Senior Clinical Research Associate include: 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. Compensation for the Senior Clinical Research Associate includes: 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-Ljbffr

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