Clinical Research Coordinator - Medical Assistant (Unblinded)

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    "html_title": "CLEAR CHOICE DERMATOLOGY LLC - Clinical Research Coordinator - Medical Assistant (Unblinded)",
    "description_html": "<p>We are seeking a dedicated and detail-oriented Clinical Research Coordinator with a Medical Assistant background to join our dynamic research team. This role offers an exciting opportunity to contribute to cutting-edge clinical trials, ensuring the integrity of drug accountability and proper dispensing of blinded medications to participants. The ideal candidate will be committed to maintaining high standards of accuracy, compliance, and participant safety in a fast-paced research environment. &nbsp;</p><p><br></p><p>Key Responsibilities &nbsp;</p><p>- Perform drug accountability activities, including inventory management, documentation, and reconciliation of study medications. &nbsp;</p><p>- Dispense blinded study drugs to clinical trial participants in accordance with protocol guidelines. &nbsp;</p><p>- Maintain accurate records of drug dispensation, returns, and wastage, ensuring compliance with regulatory standards. &nbsp;</p><p>- Assist with participant visits, including preparation of study materials and collection of relevant data. &nbsp;</p><p>- Support the research team in adhering to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. &nbsp;</p><p>- Communicate effectively with participants, staff, and sponsors regarding medication procedures and study updates. &nbsp;</p><p>- Ensure proper storage, handling, and documentation of investigational products. &nbsp;</p><p><br></p><p>This position can be part time or full time. For part time about 10 hours every 2 weeks or Medical Assistant 30h per week.&nbsp;</p><p>The position is about 20% Clinical Coordinator tasks and 80% Medical Assistant tasks- This is a new position with growing opportunity. &nbsp;</p>",
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      "title": "Clinical Research Coordinator - Medical Assistant (Unblinded)",
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      "description": "<p>Description</p><p>We are seeking a dedicated and detail-oriented Clinical Research Coordinator with a Medical Assistant background to join our dynamic research team. This role offers an exciting opportunity to contribute to cutting-edge clinical trials, ensuring the integrity of drug accountability and proper dispensing of blinded medications to participants. The ideal candidate will be committed to maintaining high standards of accuracy, compliance, and participant safety in a fast-paced research environment.  </p><p><br/></p><p>Key Responsibilities  </p><p>- Perform drug accountability activities, including inventory management, documentation, and reconciliation of study medications.  </p><p>- Dispense blinded study drugs to clinical trial participants in accordance with protocol guidelines.  </p><p>- Maintain accurate records of drug dispensation, returns, and wastage, ensuring compliance with regulatory standards.  </p><p>- Assist with participant visits, including preparation of study materials and collection of relevant data.  </p><p>- Support the research team in adhering to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.  </p><p>- Communicate effectively with participants, staff, and sponsors regarding medication procedures and study updates.  </p><p>- Ensure proper storage, handling, and documentation of investigational products.  </p><p><br/></p><p>This position can be part time or full time. For part time about 10 hours every 2 weeks or Medical Assistant 30h per week. </p><p>The position is about 20% Clinical Coordinator tasks and 80% Medical Assistant tasks- This is a new position with growing opportunity.  </p><p>Requirements</p><p><strong>Qualifications</strong></p><p> </p><p>Skills and Qualifications  </p><p>- Certified Medical Assistant or equivalent healthcare certification.  </p><p>- Prior experience in clinical research, preferably with drug dispensing and accountability.  </p><p>- Knowledge of clinical trial protocols, GCP, and regulatory requirements.  </p><p>- GCP certified or able to become certified</p><p>- Familiar with SOP</p><p>- Strong organizational skills and attention to detail.  </p><p>- Excellent communication and interpersonal skills.  </p><p>- Ability to work independently and as part of a multidisciplinary team.  </p><p>- Proficiency in electronic data capture systems and Microsoft Office Suite.  </p><p>Join our innovative team committed to advancing medical research and improving patient outcomes. We offer a collaborative work environment, opportunities for professional growth, and comprehensive benefits to support your career development.</p>",
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