Data Coordinator

Sarah Cannon Research Institute; Orlando (FL); On-site; USD 52,000 - 76,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization enabling community-based clinical trials across the United States. The Data Coordinator role supports the Study Coordinator to meet trial data deadlines, collect source documentation, complete case report forms, and track SAE reporting and visit logs.

SCRI emphasizes regulatory compliance (GCP/ICH) and SOP adherence while offering opportunities to contribute to drug development data operations and broader cancer

Qualifications

• Knowledge of scientific, medical, and regulatory terms.
• Knowledge of GCP and GMP.
• Detail-oriented.
• Excellent English written and oral skills.
• Bachelor Degree preferred.
• Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred.

Responsibilities

• 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 assistthe Study Coordinator with case report form completion and query resolution.
• You willassistin Serious Adverse Event (SAE) reporting and tracking.
• You will create andmaintainpatient visit tracking spreadsheets for the Study Coordinator.
• You willmaintainand 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 clinicaltrialyou will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.

Education

Bachelor degree

Job description

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 dailybasis,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 willassistthe Study Coordinator with case report form completion and query resolution
• You willassistin Serious Adverse Event (SAE) reporting and tracking
• You will create andmaintainpatient visit tracking spreadsheets for the Study Coordinator
• You willmaintainand 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 clinicaltrialyou will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines

What you should have for this role:

• Knowledge of scientific, medical, and regulatory terms
• Knowledge of GCP and Good Manufacturing Practice (GMP)
• Detail-oriented
• Excellent English written and oral skills.
• Bachelor Degreepreferred.
• Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings.

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That's why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

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.