JOB SUMMARY
The Associate Project Manager, Research Data is responsible for ensuring the integrity and quality of clinical research data in the Wake Forest Alzheimer's Disease Research Center.
Under general supervision, this position is a key contributor to ensuring the accuracy and completeness of clinical research data, actively contributing to the enhancement and maintenance of Electronic Data Capture (EDC) systems, and fostering data quality improvements.
This position will work as part of a team of coordinators overseeing study activities and data management for the Alzheimer’s Disease Research Center (ADRC), which is home to a large portfolio of research studies and clinical trials.
The ADRC focuses on research, education, and potential treatments aimed at treating and preventing Alzheimer’s disease and cognitive decline.
The ADRC work environment prioritizes diversity in perspective, inclusion of staff and study participants with different backgrounds, and teamwork.
The candidate for this position must also be committed to upholding these values.
The candidate should be a strong team player, thorough attention to detail, and strong analytical skills.
EDUCATION/EXPERIENCE
Bachelor’s degree in Computer Science, Psychology, or other relevant discipline with two years of experience performing data and systems-oriented duties in a research setting; or, an equivalent combination of education and experience.
Experience two years survey research experience including interviewing, supervision of data collection procedures, and training preferred.
SKILLS/QUALIFICATIONS
Strong oral, written, and interpersonal communication skills.
Demonstrates teamwork and professionalism.
Demonstrates strong analytical and problem-solving skills.
Demonstrated cultural competency and sensitivity.
Ability/temperament to adapt to changing conditions and diverse job tasks.
Strong initiative and ability to work independently.
Knowledge of computer systems and applications, including Excel software.
ESSENTIAL FUNCTIONS
Conduct routine audits of data entry to verify completeness, correctness, and consistency.
Collaborate with clinical research teams to identify data discrepancies, anomalies, and inconsistencies, and work towards their resolution.
Actively participate in the development and implementation of strategies to improve data quality across clinical trials.
Provide suggestions for process improvements to streamline data collection and management.
Administer cognitive measures as per clinical trial protocols.
Audit cognitive measure charts, ensuring accurate and consistent scoring; provide guidance, training, and support to other cognitive raters to maintain uniformity in test administration and scoring.
Collaborate with the clinical research team to contribute to the creation and refinement of comprehensive Standard Operating Procedures (SOPs) for EDC data entry and usage.
Work with study team members to update and maintain EDC systems, including REDCap.
Provide training and assistance to research staff on EDC usage and troubleshoot issues as they arise.
Monitor and troubleshoot website issues, ensuring its functionality and responsiveness.
Performs other related duties incidental to the work described herein.
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