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Clinical Research Coordinator - St. Lawrence Health System

Rochester Regional Health

City of Rochester (NY)

On-site

USD 47,000 - 64,000

Full time

6 days ago

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Job summary

Rochester Regional Health is seeking a Clinical Research Coordinator for its St. Lawrence Health System. The role involves conducting clinical trials, managing data integrity, and ensuring compliance with protocols. Ideal candidates will have an Associate Degree and relevant certification, with a passion for improving community health through research.

Qualifications

Must have an Associate Degree or equivalent experience.
ACRP or SOCRA certification required within one year.
1-3 years of healthcare or related science experience preferred.

Responsibilities

Conducts clinical research trials and assists physicians.
Manages data collection and adheres to study protocols.
Obtains informed consent and coordinates subject visits.

Skills

Data Management

Informed Consent

Statistical Analysis

Education

Associates Degree

Bachelor’s Degree in Biology or Healthcare

Clinical Research Coordinator - St. Lawrence Health System

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Clinical Research Coordinator - St. Lawrence Health System

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Job Title: Clinical Research Coordinator

Department: Research

Location: Potsdam, NY

Hours Per Week: 40 scheduled weekly hours

Schedule: 8 hour shift, 8a-4:30p, once a month on call responsibility

Summary

Conducts and assists in the System physician and staff’s clinical research trials and projects. Obtains informed consent, collects, maintains, and processes study information and research data in strict accordance with specified research and clinical protocol.

Responsibilities

Data Management Duties As applicable for both industry trials and investigator initiated projects: o Collects, processes, and assists in the compilation and verification of research data, following strict protocol and detail instructions. o Enters data into Electronic Data Capture (EDC) and responds to queries in a timely manner o Assists with routine data analysis and interpretation, as specifically assigned; may utilize statistical data analysis programs and software; assists with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol.
Protocol-Specific Activities Contacts potential subjects to introduce and explain study objectives and protocol over the phone or in person
Obtains informed consent from patients interested in a research study
Coordinates and conducts clinical research subject visits, including processing and packaging any associated laboratory samples for shipment.
Performs subject recruitment, screening and retention activities as well as subject scheduling for identified clinical trials.
Follows up with subjects according to study protocol, and adheres to safety reporting regulations
Interfaces with sponsor representatives both in person and remotely to coordinate site visits, and ensure compliance with the study protocol
Research Start-Up Activities Assists in literature search, protocol writing, case report form design, and IRB submission for new System’s industry and investigator-initiated studies
Coordinates the review, submission, and execution of community partners’ IRB submissions

Required Qualifications

Associates Degree or equivalent related experience in lieu of degree
ACRP or SOCRA certification within one year of becoming eligible

Preferred Qualifications

Bachelor’s Degree in biology or healthcare related field
ACRP or SOCRA certification
1-3 years of experience in healthcare or related science field, with knowledge of medical terminology preferred.

Education

LICENSES / CERTIFICATIONS:

Physical Requirements

M - Medium Work - Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects; Requires frequent walking, standing or squatting.

For disease specific care programs refer to the program specific requirements of the department for further specifications on experience and educational expectations, including continuing education requirements.

Any physical requirements reported by a prospective employee and/or employee’s physician or delegate will be considered for accommodations.

Pay Range

$47,590.00 - $63,900.00

City

Potsdam

Postal Code

13676

The listed base pay range is a good faith representation of current potential base pay for a successful full time applicant. It may be modified in the future and eligible for additional pay components. Pay is determined by factors including experience, relevant qualifications, specialty, internal equity, location, and contracts.

Rochester Regional Health is an Equal Opportunity/Affirmative Action Employer.

Minority/Female/Disability/Veterans by a prospective employee and/or employee’s Physician or delegate will be considered for accommodations.

Seniority level

Seniority level
Entry level

Employment type

Employment type
Full-time

Job function

Job function
Research, Analyst, and Information Technology
Industries
Hospitals and Health Care

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