Data Coordinator
Sarah Cannon Research Institute
Nashville, Tunisia · ਪੂਰਾ ਸਮਾਂ
ਅਰਜ਼ੀ ਦੇਣ ਵਾਲੇ ਪਹਿਲੇ ਵਿਅਕਤੀ ਬਣੋ
- ਅਨੁਭਵ
- ਕੋਈ ਵੀ
- ਤਨਖਾਹ
- —
- ਖੁੱਲ੍ਹਣ ਵਾਲੀਆਂ ਥਾਵਾਂ
- 1
- ਪੋਸਟ ਕੀਤਾ ਗਿਆ
- 20 ਘੰਟੇ ਪਹਿਲਾਂ
- ਕੰਮ ਮੋਡ
- ਦਫ਼ਤਰ ਵਿੱਚ
- ਸਿੱਖਿਆ
- Bachelor’s degree preferred
- ਰੈਜ਼ਿਊਮੇ
- ਅਰਜ਼ੀ ਦੇਣ ਲਈ ਲੋੜੀਂਦਾ ਹੈ
ਤੁਸੀਂ ਕਿੱਥੇ ਕੰਮ ਕਰੋਗੇ
ਕੰਮ ਦਾ ਵੇਰਵਾ
Overview
Join Sarah Cannon Research Institute (SCRI), a leading community-based oncology research organization dedicated to advancing cancer treatments and improving patient outcomes globally. As part of McKesson, SCRI offers an opportunity to contribute to groundbreaking clinical trials and cancer care innovations.
Role Description
The Data Coordinator works closely with the Study Coordinator to provide essential support for clinical trials ensuring compliance with SOPs, Good Clinical Practice (GCP), and International Council for Harmonisation (ICH) guidelines. This role is critical for accurate data management and regulatory adherence throughout the trial process.
Key Responsibilities
- Assist the Study Coordinator in meeting clinical trial data submission deadlines.
- Collect and manage source documentation for trial-enrolled patients.
- Support case report form completion and resolve data queries efficiently.
- Assist with the reporting and tracking of Serious Adverse Events (SAEs).
- Maintain patient visit tracking spreadsheets and study administrative files.
- Undertake special procedural projects to optimize drug development data operations.
- Continuously evaluate clinical trial adherence to SCRI SOPs, GCP, and ICH regulations.
Required Qualifications and Skills
- Understanding of scientific, medical, and regulatory terminology.
- Familiarity with Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP) standards.
- Strong attention to detail and organizational skills.
- Excellent proficiency in written and spoken English.
- Bachelor’s degree is preferred.
- Previous experience in healthcare, clinical trials support, or the pharmaceutical industry is advantageous.
About Sarah Cannon Research Institute
SCRI is a premier oncology research network conducting community-based clinical trials. Since inception, SCRI has led in drug development with over 850 first-in-human trials and collaborations involving more than 1,300 physicians across 200+ sites in 20+ U.S. states. SCRI’s commitment is to transform cancer care by integrating clinical excellence with innovative research.
Total Rewards and Benefits
SCRI offers a comprehensive Total Rewards program including competitive pay, performance-based bonuses, long-term incentives, and extensive benefits supporting the well-being of employees. Benefits cover physical, mental, and financial health through McKesson’s offerings, reflecting tailored support for our diverse workforce.
Important Notes on Recruiting
Applicants should be cautious of fraudulent recruitment attempts impersonating McKesson or its affiliates. Official communications will never request money or sensitive financial information, nor will they operate through informal email domains or chatrooms. Official job postings are available solely on the McKesson career site.
Diversity and Inclusion
Sarah Cannon Research Institute is an equal opportunity employer, fostering diversity and inclusivity regardless of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability.