Clinical Trial Site Marketing and Sales
Chicago, ILFull-time
23–30 an hour
Behavioral Health Market Context
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Job Description
ate and up-to-date records of potential participants, recruitment activities, and screening outcomes using study-specific databases and electronic health records (EHR).
• Informed Consent: Assist in obtaining informed consent from participants, ensuring they understand the study's purpose, risks, and benefits.
• Collaboration: Work closely with clinical study coordinators, principal investigators, and research teams to meet enrollment targets and timelines.
• Reporting: Provide regular updates on recruitment progress, including metrics such as the number of screened, eligible, and enrolled participants.
• Compliance: Ensure that recruitment activities comply with ethical guidelines, Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and all applicable regulations.
• Education & Advocacy: Educate potential participants about the importance of clinical trials and how they contribute to advancements in medical research.
• Marketing & Communication: Assist in the development of recruitment materials such as brochures, advertisements, and online campaigns to attract participants.
Qualifications:
• Previous experience in clinical research, patient recruitment, or a related healthcare role is preferred.
• Strong understanding of clinical trial processes and ethical considerations in recruitment.
• Excellent communication and interpersonal skills, with the ability to interact with diverse populations.
• Ability to work independently and as part of a team in a fast-paced, dynamic environment.
• Proficiency in using electronic medical records (EMR) systems, clinical trial management systems (CTMS), and basic office software (Microsoft Office Suite).
• Ability to drive to health fairs and patient advocacy events.
Company DescriptionWe offer a supportive work environment, opportunities for professional growth, and a competitive salary. Research by Design is a female and minority owned company that focuses upon all phases of clinical research.
• Informed Consent: Assist in obtaining informed consent from participants, ensuring they understand the study's purpose, risks, and benefits.
• Collaboration: Work closely with clinical study coordinators, principal investigators, and research teams to meet enrollment targets and timelines.
• Reporting: Provide regular updates on recruitment progress, including metrics such as the number of screened, eligible, and enrolled participants.
• Compliance: Ensure that recruitment activities comply with ethical guidelines, Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and all applicable regulations.
• Education & Advocacy: Educate potential participants about the importance of clinical trials and how they contribute to advancements in medical research.
• Marketing & Communication: Assist in the development of recruitment materials such as brochures, advertisements, and online campaigns to attract participants.
Qualifications:
• Previous experience in clinical research, patient recruitment, or a related healthcare role is preferred.
• Strong understanding of clinical trial processes and ethical considerations in recruitment.
• Excellent communication and interpersonal skills, with the ability to interact with diverse populations.
• Ability to work independently and as part of a team in a fast-paced, dynamic environment.
• Proficiency in using electronic medical records (EMR) systems, clinical trial management systems (CTMS), and basic office software (Microsoft Office Suite).
• Ability to drive to health fairs and patient advocacy events.
Company DescriptionWe offer a supportive work environment, opportunities for professional growth, and a competitive salary. Research by Design is a female and minority owned company that focuses upon all phases of clinical research.
Qualifications
- •Strong understanding of clinical trial processes and ethical considerations in recruitment
- •Excellent communication and interpersonal skills, with the ability to interact with diverse populations
- •Ability to work independently and as part of a team in a fast-paced, dynamic environment
- •Proficiency in using electronic medical records (EMR) systems, clinical trial management systems (CTMS), and basic office software (Microsoft Office Suite)
- •Ability to drive to health fairs and patient advocacy events
Benefits
- •Company DescriptionWe offer a supportive work environment, opportunities for professional growth, and a competitive salary
Responsibilities
- •Participant Recruitment: Develop and implement outreach strategies to identify and recruit potential participants for clinical research studies
- •Outreach & Engagement: Build and maintain relationships with local healthcare providers, community organizations, and patient advocacy groups to increase awareness of ongoing clinical trials
- •Database Management: Maintain accurate and up-to-date records of potential participants, recruitment activities, and screening outcomes using study-specific databases and electronic health records (EHR)
- •Informed Consent: Assist in obtaining informed consent from participants, ensuring they understand the study's purpose, risks, and benefits
- •Collaboration: Work closely with clinical study coordinators, principal investigators, and research teams to meet enrollment targets and timelines
- •Reporting: Provide regular updates on recruitment progress, including metrics such as the number of screened, eligible, and enrolled participants
- •Compliance: Ensure that recruitment activities comply with ethical guidelines, Good Clinical Practice (GCP), Institutional Review Board (IRB) requirements, and all applicable regulations
- •Education & Advocacy: Educate potential participants about the importance of clinical trials and how they contribute to advancements in medical research
- •Marketing & Communication: Assist in the development of recruitment materials such as brochures, advertisements, and online campaigns to attract participants
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