Data Coordinator job in Brentwood, TN
Vacancy has expired
Brentwood, TN CorTech LLC
| Job Ref: | 368874 |
| Employer: |
CorTech LLC |
| Job Type: | Contract |
| Salary and Benefits: | 24.00/Per Hour |
| Remote: | No |
Location |
|
| City: | Brentwood, TN |
| Post Code: | 37027 |
| Map: |
|
Description |
|
|
JobsRUs.com is seeking to hire a Data Coordinator for our client in Brentwood, TN! Benefits Available! Weekly Pay! Pay Rate - $24/hr 1st Shift: 8am-4pm Job Description The Data Coordinator is responsible for EMR data abstraction, EDC data capture, assisting with AE/SAE reporting and study queries. Ensures all activities are conducted according to company SOPs, and all applicable GCP and ICH regulations and guidelines. Major Responsibilities: Duties include but are not limited to: x Support data entry activities to meet study data needs and deadlines x Data abstraction from diverse sources x Obtain source documentation for patients enrolled into clinical trials and data registry x Maintain Data Registry as directed x Assist with Data validation, conflict resolution and quality assurance x Supports Clinical Project Manager to meet industry trial data deadlines x Obtain source documentation for patients enrolled into clinical trial x Assist Clinical Project Manager with case report form completion x Assist Clinical Project Manager with query resolution x Assist in SAE reporting and tracking x Create and maintain patient visit tracking spreadsheets x Maintain and archive study documents x Meet with clinical study sponsor representatives as requested x Develop and maintain file management and collaboration systems x Maintain calendar x Initiate improvements, tools, processes, and forms to enhance the efficiency and quality of work x Attend meetings as assigned and report on actions x Participate in educational activities and programs x Maintain strictest confidentiality x Work closely and effectively with all other department colleagues x Assist other staff as requested and performing other related work as needed. x Throughout the conduct of the clinical trial assesses adherence to HRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines x All other duties as assigned Education & Experience: x High school diploma or equivalent is required. x Bachelor?s Degree is preferred. x 1+ years of experience in healthcare, research, or other science related field Knowledge, Skills, Abilities, Behaviors: Knowledge: x Knowledge of scientific, medical, and regulatory terms x Must have an understanding of clinical research process x Knowledge of GCP and GMP Skills: The proficiency to perform a certain task x Professional writing and communicating skills required x Organizational and prioritization skills required x Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel x High computer literacy and ability to learn new software if required Abilities: An underlying, enduring trait useful for performing duties x Ability to work both collaboratively and independently x Interpersonal skills, detail oriented, and meticulous x Ability to multi-task in fast paced environment is essential. x Ability to manage, organizes, and makes decisions | |
ref: (368874)
137 days ago
Back to search results