Clinical Research Coordinator

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is hiring a Clinical Research Coordinator for its blood cancer and bone marrow transplant research program. The role oversees clinical operations, including patient enrollment, regulatory and quality activities, study data and documentation, and coordination with site staff and study teams.

Responsibilities

You will support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements

You will review the study design and inclusion/exclusion criteria with physicians and patients

You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements

You will collect, complete, and enter data into study specific case report forms (CRFs) or electronic data capture systems within study required timelines

You will ensure the integrity of the data submitted on case report forms or other data collection tools by careful source document review and monitoring data for missing or implausible data

You will create study specific tools for source documentation when not provided by sponsor

You will generate and track drug shipments, lab kits, and other supplies

You will be responsible for accurate and complete documentation of protocol requirements according to site work instructions and standard operating procedures (SOPs)

You will track and report adverse events, serious adverse events, protocol waivers, and deviations

You will maintain accurate and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications

You will coordinate regular site research meetings

You will attend study-specific on-site meetings/visits, investigator meetings, conference calls, and other coordinator meetings, as required and you will work closely with monitors, study teams and site staff to ensure quality study data

You will communicate site status through a weekly activity report to appropriate site/management colleagues

Preferred

preferably a Bachelor's Degree

preferably in hematology/oncology and/or transplant

At least one year of experience managing blood cancer and/or BMT clinical trials

Research certification (ACRP or CCRP)

RN or LPN

Bachelor’s degree

Hematology/oncology

Transplant expertise

Clinical trial management

Blood cancer trials

BMT clinical trials

ACRP certification

CCRP certification

RN

LPN

Benefits

Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being

Annual bonus or long-term incentive opportunities may be offered

Company

Healthcare products, services, and insights for providers and pharmacies

Irving, Texas, USA

http://www.mckesson.com/

Founded in 1833

10001+ employees

Qualifications

An Associate's Degree

Knowledge of medical and research terminology

Knowledge of FDA Code of Federal Regulations and GCP

Knowledge of the clinical research processes

Public presentation skills

The ability to manage multiple ongoing priorities and projects with a diverse team of professionals

At least one year of oncology experience

At least one year of experience in a clinical research setting

Preferably a Bachelor's Degree

Preferably in hematology/oncology and/or transplant

At least one year of experience managing blood cancer and/or BMT clinical trials

Research certification (ACRP or CCRP)

RN or LPN

Required skills

Clinical Research, Oncology, Hematology/Oncology, Bone Marrow Transplant (BMT), FDA Code of Federal Regulations, Clinical Practice (GCP), ACRP Certification, CCRP Certification, Registered Nursing (RN), Licensed Practical Nursing (LPN), Medical and Research Terminology

Preferred skills

preferably a Bachelor's Degree, preferably in hematology/oncology and/or transplant, Research certification (ACRP or CCRP), RN or LPN

Experience

1+ years