Data Coordinator at HCA Healthcare in Nashville, Tennessee

Posted in Other 21 days ago.





Job Description:

Description

SHIFT: No Weekends
SCHEDULE: Full-time


Sarah Cannonis the research arm of HCA's global cancer enterprise. Focused on advancing therapies for patients, it is one of the world's leading clinical research organizations conducting community-based clinical trials in oncology, cardiology and orthopedics through affiliations with a network of more than 1,000 physicians across the United States and United Kingdom.



We believe our success is dependent on a healthy work environment where staff members are the core of advancing therapies for patients and accelerating drug development. We apply the same compassion and commitment we have for our patients to our co-workers and colleagues and promote an entrepreneurial culture.

Benefits:


  • Tuition Reimbursement/Assistance Programs

  • Student Loan Repayment

  • Paid Personal Leave

  • 401k (100% annual match - 3%-9% of pay based on years of service)

  • Identity Theft Protection discounts

  • Auto, Home, and Life Insurance options

  • Adoption Assistance

  • Employee Stock Purchase Program (ESPP)

The Data Coordinator provides support to Clinical Trial Specialist (CTS) 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 supports CTS to meet industry trial data deadlines

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

  • You will assist CTS 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 CTS

  • 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.

Qualifications

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 Degree preferred.

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

Do you want to be on a team fighting cancer together? Apply today!

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.

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