Data Coordinator

It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. Our Mission People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting‑edge research, SCRI is redefining cancer care around the world. Data Coordinator The Data Coordinator provides support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis, ensures all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines. Responsibilities You will support CRC to meet industry trial data deadlines You will obtain source documentation for patients enrolled onto clinical trials You will assist CRC with case report form completion and with query resolution You will assist in Serious Adverse Event (SAE) reporting and tracking You will create and maintain patient visit tracking spreadsheets for CTS You will maintain and archive study administrative files You will maintain and archive regulatory files You will assist in ensuring source document templates are accurate. You will be assigned special procedural projects to enhance the functioning of the research program Throughout the conduct of the clinical trial you will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines. Qualifications Knowledge of scientific, medical, and regulatory terms; Knowledge of GCP and Good Manufacturing Practice (GMP) Detail-oriented Excellent English written and oral skills Bachelor Degree preferred Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred The compensation range for this position is $24/hr - $27/hr. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. #J-18808-Ljbffr McKesson