What are the responsibilities and job description for the Data Coordinator position at swipejobs?
Job Description:
Are you a detail-oriented and organized Data Coordinator located near Brentwood, TN? Do you have at least 1 year of experience in healthcare, research, or other science related field?
Apply today to join a team where your growth, well-being, and success are our top priority!
Details:
$ 24.00/hr
HV23
#HV23
Are you a detail-oriented and organized Data Coordinator located near Brentwood, TN? Do you have at least 1 year of experience in healthcare, research, or other science related field?
Apply today to join a team where your growth, well-being, and success are our top priority!
Details:
- $24 per hour pay rate
- Full Time
- Contract
- Onsite in Brentwood, TN
- Schedule: 8am - 4pm M-F
- Health, Dental, Vision insurance offered
- 401k options
- Work with a great team!
- High School Diploma - Required
- Bachelor's Degree - Preferred
- 1 years of experience in healthcare, research, or other science related field - Required
- Knowledge of scientific, medical, and regulatory terms
- Must have an understanding of clinical research process
- Knowledge of GCP and GMP
- Professional writing and communicating skills required
- Organizational and prioritization skills required
- Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel
- High computer literacy and ability to learn new software if required
- Support data entry activities to meet study data needs and deadlines
- Data abstraction from diverse sources
- Obtain source documentation for patients enrolled into clinical trials and data registry
- Maintain Data Registry as directed
- Assist with data validation, conflict resolution, and quality assurance
- Support Clinical Project Manager to meet industry trial data deadlines
- Obtain source documentation for patients enrolled into clinical trial
- Assist Clinical Project Manager with case report form completion
- Assist Clinical Project Manager with query resolution
- Assist in SAE reporting and tracking
- Create and maintain patient visit tracking spreadsheets
- Maintain and archive study documents
- Meet with clinical study sponsor representatives as requested
- Develop and maintain file management and collaboration systems
- Maintain calendar
- Initiate improvements, tools, processes, and forms to enhance the efficiency and quality of work
- Attend meetings as assigned and report on actions
- Participate in educational activities and programs
- Maintain strictest confidentiality
- Work closely and effectively with all other department colleagues
- Assist other staff as requested and perform other related work as needed
- Throughout the conduct of the clinical trial, assess adherence to HRI SOPs, Good Clinical Practice (GCP), and ICH regulations and guidelines
$ 24.00/hr
HV23
#HV23
Salary : $24