Clinical Data Associate Job Description Template
Our company is looking for a Clinical Data Associate to join our team.
Responsibilities:
- Conduct data quality checks and data reviews;
- Work in a team environment to support eCRF design and end user testing;
- Support data abstraction and data entry of assigned studies, gather and enter data in accordance with SOPs and protocol specific processes;
- Participate in cross-functional process initiatives and clinical research team meetings;
- Adhere to NIH Clinical Data Management project timelines on multiple complex protocols;
- Develop protocol specific data management plans ensuring alignment with protocol and data quality standards;
- Abstract and grade adverse events based on the protocol specifications and SOPs;
- Other duties as assigned.
Requirements:
- Knowledge of Veeva Trial Master File or other document repository experience;
- Associate or B.S. in Nursing or other clinical science;
- Excellent verbal and written skills;
- Able and willing to work on call rotational shift as needed, which may include weekends and holidays;
- Proficient with Microsoft Office Applications (Word, Excel, PowerPoint);
- Fluency in other languages is a plus;
- Minimum of one (1) year wound care experience in a private, public, government, or military environment;
- Would like someone who has some expereince with Unit Acceptance Testing (UAT);
- Associate’s Degree/Technical Diploma or higher (completed and verified prior to start) from an accredited institution;
- Active/unrestricted/unencumbered LVN or RN license to practice nursing in any state;
- Good communication skills;
- Experience with clinical trial databases and electronic data capture (EDC);
- Experience with clinical/medical terminology;
- Bachelor’s degree in life sciences or related field;
- Knowledge of Federal information technology, the Biotech or Pharmaceutical Industry, or equivalent comparable background.