Clinical Research Coordinator

Astera Cancer Care; Nashville (TN); On-site; USD 52,000 - 76,000; Full time

Job summary

Tennessee Oncology in Nashville seeks a Clinical Research Coordinator to join the research team and support a range of clinical trials and observational studies. You will learn and assist with screening, consent, data collection, and biospecimen handling to support quality research.

Ideal candidates have a bachelor’s degree and at least one year of related experience, strong communication, organization, and the ability to work in a fast-paced environment alongside clinicians and researchers.

Qualifications

• Bachelor’s Degree or equivalent combination of education and experience.
• One year of relevant experience or work in a medical and/or laboratory facility.

Responsibilities

• Screens potential subjects for eligibility against trial criteria.
• Assists with recruitment of subjects to trials.
• Maintains informed consent records for the duration of a study.
• Procures, processes, and ships biospecimens per protocol.

Skills

Verbal communication

Written communication

Organization

Prioritization

Clinical trials

Team collaboration

MS Office

Bilingual EN/ES

Education

Bachelor’s Degree or equivalent

Job description

Tennessee Oncology, one of the nation’s largest, community-based cancer care specialists, is home to one of the leading clinical trial networks in the country. Established 1976 in Nashville, Tennessee Oncology’s mission remains unchanged: To provide access to high-quality cancer care and the expertise of clinical research for all patients, at convenient locations within their community and close to their home. Our growing network of physicians and locations is based on this mission. Tennessee Oncology is committed to advancing both the science of detection and targeted treatments, and to making these advances available to every patient. We believe caring for cancer patients is a privilege.

Why Join Us?

We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.

Job Description

This position works closely with the research team to learn and assist with a variety of clinical research activities.

ESSENTIAL FUNCTIONS

• Screens potential subjects for eligibility to prospective/observational trials through a careful review of the patient’s past medical history and a review of current findings against inclusion and exclusion criteria specific to a trial
• Assists with recruitment of subjects to prospective/observational trials through a variety of methods
• Maintains informed consents records of each patient for the duration of a study
• Procures, processes, and ships biospecimens per sponsor protocol and regulations
• Protects the rights, safety, and welfare of patients
• Strives to maintain harmonious relationships with clinic personnel, administrative staff, patients, their caregivers, and the public
• Reviews newly activated protocols, amendments, notices, suspensions, and terminations
• Responsible for maintaining current knowledge of the Code of Federal Regulations and International Council for Harmonization Guidelines
• Maintains required certification in Good Clinical Practice, Human Subjects Protections, and biological shipping training
• Serves as a liaison to multiple Tennessee Oncology departments, providers, and other personnel regarding research protocols and regulatory compliance
• Maintains a professional approach respecting the dignity and confidentiality of patients
• Maintains a good attendance record and reports to work on time
• Maintains a professional attitude and appearance
• Maintain Tennessee licensure as applicable
• Performs other duties as assigned

KNOWLEDGE, SKILLS & ABILITIES

• Excellent verbal and written communication skills
• Excellent organization and follow-up skills
• Ability to handle multiple priorities in a fast-paced environment
• Ability to understand complex clinical trials protocols
• Ability to function in multi-functional teams
• Microsoft Office product knowledge (Word, Excel, PowerPoint, etc.)
• Bilingual (English/Spanish) a plus

EDUCATION & EXPERIENCE

• Bachelor’s Degree or equivalent combination of education and experience required
• One year of relevant experience or work in a medical and/or laboratory facility required

Thank you for your interest in Tennessee Oncology. People like yourself have helped us grow into one of the largest and most influential oncology practices in the country. Our front line heroes are beloved by our patients and their families. Caring for cancer patients is a privilege.