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Clinical Research Study Jobs in Rochester, NY (NOW HIRING)

Lancesoft INC

Nurse Practitioner

Rochester, NY · Remote

$40 - $44.44/hr

Experience working on academic or federally funded research studies. * Experience with clinical research and/or human subject's research. * Experience reviewing laboratory and medical history data ...

Neko Health

Breast Sonographer

Farmington, NY · On-site

Role Purpose We are looking for an experienced Breast Ultrasound Sonographer to join our clinical team in New York City and perform breast ultrasounds as part of a clinical research study. This role ...

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All JobsClinical Research Study JobsClinical Research Study Jobs in Rochester, NY

Clinical Research Study information

See Rochester, NY salary details

$13

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How much do clinical research study jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for clinical research study in Rochester, NY is $23.77, according to ZipRecruiter salary data. Most workers in this role earn between $19.90 and $24.42 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in clinical research studies, and why are they important?

To thrive in clinical research studies, you need a background in life sciences or healthcare, strong analytical skills, and knowledge of research methodologies, often supported by a degree in a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing protocols, collaborating with teams, and maintaining regulatory compliance. These competencies ensure the integrity of research data, patient safety, and the successful execution of clinical trials.

What qualifications do you need to be a clinical research study?

A clinical research study is not a job but a type of research; however, professionals involved typically need a relevant degree in healthcare, life sciences, or a related field, along with knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements. Skills in data collection, patient interaction, and familiarity with clinical trial protocols are also important. Certification such as Certified Clinical Research Professional (CCRP) can enhance qualifications.

What are some common challenges faced by professionals working in clinical research studies, and how can they be addressed?

Professionals involved in clinical research studies often face challenges such as patient recruitment, maintaining regulatory compliance, and ensuring accurate data collection. Recruitment can be difficult due to strict inclusion criteria or participant hesitancy, but building partnerships with healthcare providers and clear communication can help. Staying updated on regulatory requirements and utilizing electronic data capture systems can streamline compliance and data accuracy. Effective teamwork and regular communication with investigators, coordinators, and sponsors are essential for addressing these challenges and ensuring study success.

What is a clinical research study?

A clinical research study is a scientific investigation involving human participants, designed to evaluate medical, surgical, or behavioral interventions. These studies help determine the safety and effectiveness of new treatments, drugs, medical devices, or procedures. Clinical research can include clinical trials, observational studies, and longitudinal studies. Participation is usually voluntary, and studies are conducted under strict ethical guidelines to protect participants' rights and safety.

What is the difference between Clinical Research Study and Clinical Research Coordinator?

AspectClinical Research StudyClinical Research Coordinator
RoleParticipates in designing, conducting, and analyzing clinical trialsManages daily trial operations, patient recruitment, and data collection
Required CredentialsOften requires clinical research training, degrees in health sciences, or related certificationsTypically requires similar certifications, with additional experience in patient interaction
Work EnvironmentResearch labs, hospitals, or clinical trial sitesClinical trial sites, hospitals, or research facilities
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, research organizations, pharmaceutical companies

While a Clinical Research Study involves designing and analyzing trials, a Clinical Research Coordinator focuses on managing trial operations and patient interactions. Both roles require similar credentials and work in related environments, but their responsibilities differ significantly.

What can I do with a clinical research study degree?

A degree related to clinical research studies prepares individuals for roles such as clinical research coordinator, data manager, or regulatory specialist. These positions involve managing clinical trials, ensuring compliance with protocols, and working with research teams using tools like electronic data capture systems. Opportunities exist in pharmaceutical companies, research institutions, and healthcare organizations.
What are the most commonly searched types of Clinical Research Study jobs in Rochester, NY? The most popular types of Clinical Research Study jobs in Rochester, NY are:
Clinical Research Study jobs near you
Infographic showing various Clinical Research Study job openings in Rochester, 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 $49,440 per year, or $23.8 per hour.

Nurse Practitioner

Lancesoft INC

Rochester, NY • Remote

$40 - $44.44/hr

Contractor

Posted 27 days ago

Job description

Title: Nurse Practitioner – Remote Research Study Reviewer

Position: Remote - Part Time

Work Hours:

  • Anticipate up to 10 participants per week
  • Each participant review is anticipated to require approximately 30 minutes to 1 hour
  • Flexible remote schedule, in coordination with research staff and participant schedules


Pay range: $40.00/hr. - $44.44 /hr.

Job Description:

Position Summary:

The individual will remotely review participant eligibility, assess inclusion and exclusion criteria, and assist with protocol-directed clinical oversight for research participants.

This position is ideal for a clinician with experience in clinical research, protocol compliance, and telemedicine-based participant interactions.

Primary Responsibilities:

  • Review participant medical information to determine eligibility based on study inclusion and exclusion criteria.
  • Conduct remote/telemedicine-based participant assessments as required by study protocols.
  • Review and authorize serial blood draws according to protocol requirements.
  • Coordinate or assist with ordering medical and research-related supplies.
  • Document eligibility determinations and protocol reviews in accordance with institutional and regulatory requirements.
  • Communicate with study coordinators and research staff regarding participant eligibility and protocol compliance.
  • Ensure adherence to human subject’s research regulations and institutional policies.

Required Qualifications:

  • Current licensure as a Nurse Practitioner in New York.
  • Strong clinical judgment and attention to detail.
  • Ability to work independently in a remote environment.
  • Excellent written and verbal communication skills.

Required Training

  • Current CITI Human Subjects Research Training certification required prior to study participation.

 

Preferred Qualifications

  • Experience with telemedicine platforms.
  • Experience working on academic or federally funded research studies.
  • Experience with clinical research and/or human subject’s research.
  • Experience reviewing laboratory and medical history data for study eligibility.
  • Experience with IRB-regulated clinical research environments.
  • Experience or familiarity with research protocols and inclusion/exclusion review processes.
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About LanceSoft

Sourced by ZipRecruiter

Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Herndon, VA, US

Year founded

2000

Social media

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