Hospital Corporation of America

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Data Coordinator

at Hospital Corporation of America

Posted: 3/1/2019
Job Status: Full Time
Job Reference #: 03058-5640
Keywords:

Job Description

Sarah Cannon at HealthONE is determined to make a difference in our patients' lives. As a member of Sarah Cannon, we are a part of a network that has conducted community-based clinical trials for more than 20 years and has administered more than 225 first-in-man clinical trials to date. Sarah Cannon Research Institute has been a clinical trial leader in more than 2/3 of approved cancer therapies over the last 10 years and partners with hundreds of cancer experts engaged in clinical research across the United States and United Kingdom.

Please visit our website at: SarahCannonResearch.com/Denver

Benefits:

We offer you a generous compensation package including:paid time off, 401k, medical, dental vision and life insurance




Sarah Cannon Research Institute at HealthONE is an outpatient clinic located on the campus of Presbyterian/ St. Luke's Medical Center (P/SL).

Summary of Key Responsibilities: Provides support to clinical trial specialist (CTS) on a daily basis, ensures all activities are conducted according to company SOPs and all applicable GCP and ICH regulations and guidelines.

Duties and Responsibilities:
  • Supports CTS to meet industry trial data deadlines
  • Obtain source documentation for patients enrolled into clinical trial
  • Assist CTS with case report form completion
  • Assist CTS with query resolution
  • Assist in SAE reporting and tracking
  • Create and maintain patient visit tracking spreadsheets for CTS
  • Maintains and archives study administrative file
  • Maintains and archives regulatory files
  • Assist in ensuring Site Visit Outlines are accurate
  • Attends meetings as assigned and reports on actions.
  • Participates in educational activities and programs.
  • Maintains strictest confidentiality.
  • Works closely and effectively with all other department colleagues.
  • Assists other staff as requested and performs other related work as needed.
  • Assigned special procedural projects to enhance the functioning of Drug Development Data operations
  • Throughout the conduct of the clinical trial, assesses adherence to Sarah Cannon SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.


Qualifications

Knowledge: 
  • Knowledge of scientific, medical, and regulatory terms
  • Knowledge of GCP and GMP

Skills:

  • Proficient in Microsoft Office software, including Word, Excel, and Access; high computer literacy and ability to learn new software if required
Abilities: 
  • Detail-oriented
  • Ability to multi-task in fast paced environment is essential.
  • Interpersonal, communication, and organizational skills.
  • Ability to manage, organizes, and makes decisions.
Education:
High School Diploma required; Bachelor Degree preferred

Experience:
One year of healthcare experience preferred

Do you want to be a part of a team working together to fightcancer?


We are so excited to speak with you about this phenomenalopportunity. Apply to hear more.

 

 

We are an equal opportunity employer and value diversity atour company. We do not discriminate on the basis of race, religion, color,national origin, gender, sexual orientation, age, marital status, veteranstatus, or disability status.