Data Coordinator

About the role

The Data Coordinator provides support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis, ensuring all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines.

Responsibilities

• Supports CRC to meet industry trial data deadlines
• Obtains source documentation for patients enrolled onto clinical trials
• Aids CRC in case report form completion and query resolution
• Aids in Serious Adverse Event (SAE) reporting and tracking
• Creates and maintains patient visit tracking spreadsheets for CTS
• Maintains and archives study administrative files
• Maintains and archives regulatory files
• Assigns special procedural projects to enhance the functioning of the research program
• Affirms adherence to SCRI SOPs, GCP, and ICH regulations and guidelines throughout the clinical trial conduct

Requirements

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

Qualifications

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

Skills

• Strong organizational and time management skills
• Ability to work independently and as part of a team
• Attention to detail and accuracy in data entry and documentation
• Proficiency in Microsoft Office Suite

Benefits

Compensation range for this position is $24/hr - $27/hr. For more information regarding benefits through our parent company, McKesson, please click here.

Pay

The compensation range for this position is $24/hr - $27/hr.

Schedule

N/A

Benefits

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. For more information regarding benefits through our parent company, McKesson, please click here.

Company Information

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.

Equal Opportunity Employer

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.