Data Coordinator

McKesson; Denver (CO); On-site; USD 32,000 - 37,000; Full time

Benefits offered by this job

Total Rewards package

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Data Coordinator to support Study Coordinators, ensure SOP/GCP/ICH compliance, and manage trial data processes at SCRI’s Denver-area site.

You will handle source documentation, CRF completion, SAE reporting, and data-tracking tasks while helping maintain study files and participate in special projects to improve data operations.

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's degree preferred.
• Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred.

Responsibilities

• Support Study Coordinators to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled into clinical trial.
• Assist Study Coordinators 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 Study Coordinators.
• Maintain and archive study administrative files.
• Contribute to special procedural projects to enhance Drug Development Data Operations.
• Assess adherence to SCRI SOPs, GCP, and ICH regulations during trials.

Skills

GCP knowledge

GMP knowledge

Detail-oriented

English proficiency

Education

Bachelor's degree preferred

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 Coordinators 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 Study Coordinators to meet industry trial data deadlines


• You will obtain source documentation for patients enrolled into clinical trial


• You will assist Study Coordinators 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 Study Coordinators


• 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.

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's degree preferred.


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

Pay range $23/hr - $27/hr

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.

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.

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.