Data Coordinator

Sarah Cannon Research Institute • Orlando, FL

1d

About The Position

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. The Data Coordinator provides support to Study Coordinator 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. You will support the Study Coordinator to meet industry trial data deadlines You will obtain source documentation for patients enrolled into clinical trial You will assist the Study Coordinator with case report form completion and query resolution You will assist in Serious Adverse Event (SAE) reporting and tracking You will create and maintain patient visit tracking spreadsheets for the Study Coordinator You will maintain and archive study administrative files You will be assigned special procedural projects to enhance the functioning of Drug Development Data Operations Throughout the conduct of the clinical trial you will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines

Requirements

• Knowledge of scientific, medical, and regulatory terms
• Knowledge of GCP and Good Manufacturing Practice (GMP)
• Detail-oriented
• Excellent English written and oral skills

Nice To Haves

• Bachelor Degree preferred
• Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred

Responsibilities

• support to Study Coordinator 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
• support the Study Coordinator to meet industry trial data deadlines
• obtain source documentation for patients enrolled into clinical trial
• assist the Study Coordinator with case report form completion and query resolution
• assist in Serious Adverse Event (SAE) reporting and tracking
• create and maintain patient visit tracking spreadsheets for the Study Coordinator
• maintain and archive study administrative files
• assigned special procedural projects to enhance the functioning of Drug Development Data Operations
• assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 501-1,000 employees