Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Clinical Data Entry Specialist
Job
Orange County Research Center
Lake Forest, CA (In Person)
Full-Time
Review key factors to help you decide if the role fits your goals.
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
37
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Orange County Research Center in Lake Forest is seeking a meticulous and detail-oriented Data Entry Specialist to join our team which is focused on clinical trials and medical office research. The ideal candidates will have a comprehensive understanding of medical terminology, be a quick learner, and demonstrate the ability to adhere to Good Clinical Practice (GCP) guidelines. This position offers the opportunity to contribute to cutting-edge medical research in a dynamic and fast-paced environment.
Duties :
- Accurate entry, updating and management of data throughout various electronic data capture (EDC) systems.
- Verification of both accuracy and completeness of data entries by cross-referencing the source documents.
- Ensuring data entered meets the study protocols and GCP guidelines.
- Preparation and maintenance of detailed records of data entered.
- Working closely and communicating effectively with study staff (Coordinators, Investigator, etc.) to remain apprised of updates or changes, as appropriate, including queries, missing information, etc.
- Participate in team meetings and contribute to discussions on data management best practices.
- Stay updated on GCP guidelines and other relevant regulatory requirements.
- Attending training sessions and workshops, as needed, to enhance data entry skills and knowledge.
Requirements :
- High school diploma or equivalent; Associate degree or higher preferred, but not required.
- Proven experience in data entry, preferably in a clinical research setting.
- Familiarity with medical terminology and clinical research processes.
- Proficiency in using EDC systems and other data management tools or proven history of using and/or learning them quickly.
- Excellent attention to detail and accuracy.
- Strong organizational and time management skills.
- Ability to learn quickly and adapt to new procedures and systems.
- Knowledge of GCP guidelines and regulatory requirements a plus.
- Strong written and verbal communication skills.