Clinical Research Coordinator – St. Lawrence Health System Position Available In Monroe, New York

Job Title:

Clinical Research CoordinatorDepartment:

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.