Patient Recruitment Specialist
2 days ago
We are seeking an experienced Patient Recruitment Specialist to join our clinical research team at Research by Design, LLC. As a key member of our staff, you will develop and implement strategies to identify and recruit potential participants for our studies.
Key Responsibilities- Develop and implement effective recruitment strategies to attract potential participants for our clinical trials.
- Screen and evaluate potential participants to ensure they meet the study criteria and protocols.
- Build and maintain relationships with local healthcare providers, community organizations, and patient advocacy groups to increase awareness of our studies.
- Maintain accurate and up-to-date records of potential participants, recruitment activities, and screening outcomes using study-specific databases and electronic health records (EHR).
- Assist in obtaining informed consent from participants, ensuring they understand the study's purpose, risks, and benefits.
- Work closely with clinical study coordinators, principal investigators, and research teams to meet enrollment targets and timelines.
- Provide regular updates on recruitment progress, including metrics such as the number of screened, eligible, and enrolled participants.
- Ensure that recruitment activities comply with ethical guidelines, Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and all applicable regulations.
$65,000 - $85,000 per year, depending on experience, plus comprehensive benefits package, including medical, dental, and vision insurance, 401(k) matching, and generous paid time off.
Essential Skills- A strong understanding of clinical trial processes and ethical considerations in recruitment is required.
- Excellent communication and interpersonal skills, with the ability to interact with diverse populations, are essential.
- Ability to work independently and as part of a team in a fast-paced, dynamic environment is crucial.
- Proficiency in using electronic medical records (EMR) systems, clinical trial management systems (CTMS), and basic office software (Microsoft Office Suite) is necessary.
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