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Clinical Research Assistant
2 months ago
We are seeking a detail-oriented and motivated Clinical Research Assistant to join our team. This role will primarily focus on data entry and patient recruitment for our dermatology trials. The successful candidate will play a key role in supporting our clinical research team by ensuring accurate data management and helping to recruit and enroll participants in ongoing studies.
Key Responsibilities:
Data Entry
- Accurately enter clinical trial data into electronic data capture (EDC) systems in accordance with study protocols and GCP guidelines.
- Maintain up-to-date and accurate records of all data entry activities, ensuring data integrity and compliance with regulatory requirements.
- Perform regular quality checks on entered data to identify and correct any discrepancies or errors.
- Assist in the preparation and maintenance of source documents, case report forms (CRFs), and other study-related documentation.
- Collaborate with the clinical research team to resolve data-related queries and discrepancies promptly.
Patient Recruitment:
- Assist in identifying and screening potential study participants based on eligibility criteria outlined in study protocols.
- Conduct outreach activities to recruit participants, including phone calls, emails, and community engagement efforts.
- Schedule and coordinate participant visits, ensuring they are informed of study procedures, risks, and benefits.
- Support the informed consent process by providing potential participants with clear and accurate information about the study.
- Maintain a database of recruited participants and track their progress throughout the study, ensuring timely follow-up and retention.
- Work closely with the Clinical Research Coordinator to develop and implement effective recruitment strategies to meet study enrollment targets.
Qualifications:
Education:
- An associate’s or bachelor’s degree in a related field (e.g., life sciences, health sciences, public health) is preferred.
Experience:
- Previous experience in a clinical research or healthcare setting is preferred.
- Familiarity with data entry procedures and electronic data capture systems.
- Experience in patient recruitment and community outreach is an asset.
Skills:
- Strong attention to detail and accuracy in data entry.
- Excellent organizational and time management skills.
- Effective communication and interpersonal skills, with the ability to interact professionally with patients, study participants, and team members.
- Ability to maintain confidentiality and handle sensitive information in accordance with regulatory and ethical guidelines.
- Proficiency in Microsoft Office Suite (Word, Excel, Outlook) and experience with clinical trial management software (CTMS) or EDC systems is a plus.
Additional Requirements:
- Ability to work in a fast-paced environment and manage multiple tasks simultaneously.
- Willingness to learn and adapt to new processes and technologies related to clinical research.
- Availability to work flexible hours, including occasional evenings or weekends, depending on study requirements.
Physical Requirements:
- Ability to sit for extended periods while performing data entry tasks.
- Ability to travel locally for recruitment and outreach activities as needed.