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Clinical Research Associate Jobs in Rensselaer, NY

Research Associate, NYS PEF

Albany, NY · On-site

$70K - $100K/yr

NYS Public Employees Federation Research Associate Albany, NY Public Employees Federation (PEF) is a diverse New York State labor union representing over 55,000 professional, scientific, and ...

... clinical research standards. Responsibilities : * Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files ...

Logistics Associate - Nassau

Nassau, NY · On-site

$23.49 - $32.46/hr

... clinical research that is driving a revolution in our understanding of cancer as a disease and ... Apply now to join our team as a Logistics Associate at our Nassau location and kick start your ...

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Clinical Research Associate information

See Rensselaer, NY salary details

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How much do clinical research associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical research associate in Rensselaer, NY is $40.83, according to ZipRecruiter salary data. Most workers in this role earn between $28.65 and $52.26 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

What is the difference between Clinical Research Associate vs Clinical Trial Coordinator?

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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Infographic showing various Clinical Research Associate job openings in Rensselaer, NY as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $84,930 per year, or $40.8 per hour.

Advanced Practice Provider (Research)

Capital Cardio Associates

Albany, NY

Full-time

Medical, Dental, Retirement, PTO

Re-posted 27 days ago


Key responsibilities

  • Manage complex investigational medication protocols, perform advanced clinical assessments, and ensure patient safety across cardiovascular trials.

  • Serve as an official Sub-Investigator, perform clinical physical examinations, review medical histories, and assess patient eligibility for trial enrollment.

  • Collaborate with Principal Investigators, Clinical Research Coordinators, and external partners to maintain research standards, regulatory compliance, and study workflows.


Job description

Capital Cardiology Associates is currently seeking a highly motivated Research Advanced Practice Provider to support and expand the clinical research initiatives within our cardiology program.

The ideal candidate will have strong clinical experience, excellent coordination skills, and a keen interest in research. Our team is committed to providing the necessary training and support to facilitate professional development in this role. Moving beyond standard trial coordination, this provider will utilize their clinical scope of practice to manage complex investigational medication protocols, perform advanced clinical assessments, and ensure patient safety across our Phase II-IV cardiovascular trials.

The successful candidate will work closely with our Principal Investigators (PIs), Clinical Research Coordinators (CRCs), and clinical staff to maintain the highest standards of research operations and regulatory compliance.

Key Responsibilities:

Clinical Oversight and Sub-Investigator Duties:

  • Serve as an official Sub-Investigator (Sub-I) across multiple high-acuity cardiovascular trials.
  • Perform comprehensive clinical physical examinations, review medical histories, and determine patient eligibility for trial enrollment.
  • Formally assess, grade, and medically manage Adverse Events (AEs) and Serious Adverse Events (SAEs) in real-time.
  • Manage complex investigational medication dosing, titrations, and study drug protocols in accordance with NYS regulations and sponsor guidelines.
  • Manage study workflows, timelines, documentation, and regulatory requirements.
  • Ensure compliance with Good Clinical Practice (GCP) standards and human subject protection regulations.

Patient Care & Protocol Management:

  • Facilitate the informed consent process, ensuring patients fully understand complex clinical trial protocols, risks, and benefits
  • Review and interpret diagnostic results, including lab work and ECGs to ensure patient safety and protocol compliance
  • Provide immediate, on-site clinical guidance and support to the Clinical Research Coordinator (CRC) team during daily patient visits

Strategic Leadership & Collaboration:

  • Work directly with physician Principal Investigators (PIs) to triage clinical decisions
  • Partner with the Research Manager to evaluate incoming study pipelines, serving as the primary clinical point of contact to evaluate new trial protocols for medical feasibility, patient safety, and operational alignment.
  • Serve as a primary clinical liaison for pharmaceutical sponsors, Medical Monitors, and external partners during active study execution.
  • Provide clinical expertise and representation during internal reviews, sponsor-initiated monitoring visits, and FDA audits.

Regulatory & Quality Assurance:

  • Maintain accurate regulatory files (IRB submissions, amendments, safety reports).
  • Uphold clinical research compliance with institutional policies and federal guidelines.

Qualifications:

Required:

  • NYS NP or PA license and board certification.
  • Experience in clinical research coordination, preferably in cardiology or cardiovascular studies though new graduates are encouraged to apply.
  • Good Clinical Practice (GCP) certification (prior or must obtain upon hire).
  • Strong understanding of clinical trial operations and regulatory standards.
  • Excellent organizational, communication, and interpersonal skills.

Preferred:

  • Experience leading clinical research projects or supervising research staff.
  • Knowledge of electronic data capture systems (EDC) or clinical trial management systems (CTMS).
  • Certification such as CCRC, CCRP, or similar.

Skills:

  • Ability to manage multiple trials and deadlines concurrently.
  • High attention to detail and strong problem-solving skills.
  • Effective collaborator with clinicians, coordinators, and research partners.

Compensation:

  • $ 105,000-$ 115,000 based on experience and qualifications.

What We Offer:

  • Paid Sick and Vacation Accruals
  • Health, Dental, and FSA plans available
  • Voluntary Supplemental Benefits options
  • Generous 401k Contributions
  • Tuition Reimbursement opportunities

Equal Opportunity Employer Statement:

Capital Cardiology Associates is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state or local protected class.

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