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Essential Job Duties:Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes . The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.

<h3>Description</h3><br/><div>Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, SC, TX, VA, and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow. <br/><br/>The <strong>Principal Investigator </strong>conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.</div><br/><h3>Key Responsibilities</h3><br/><div><strong>Essential Job Duties:</strong></div><ul><li>Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes </li><li>Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance</li><li>Evaluates and assesses participants to ensure only eligible participants enroll into the trials.</li><li>Participates and engages in successful delivery and retention of study participants.</li><li>Interacts positively and collaboratively with sponsors, clients and team members.</li><li>Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.</li><li>Actively involved in protocol training for staff.</li><li>Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.</li><li>Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.</li></ul><div><br/></div><br/><h3>Skills, Knowledge and Expertise</h3><br/><div><strong>Minimum Qualifications:</strong>  MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required.  Clinical Research experience is a plus. Board certification in area of specialty is required. CPR required / ACLS preferred.<br/><br/></div><div><strong>Required Skills: </strong></div><ul><li>Clinical skills and clinical procedures based in area of specialty. </li><li>Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm). </li><li>Must possess strong organizational skills, attention to detail, and math proficiency.</li><li>Well-developed written and verbal communication skills.  Bi-lingual (English / Spanish) proficiency is highly preferred.</li><li>Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.  </li><li>Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.</li><li>Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.</li><li>Must possess a high degree of urgency, self-motivation, integrity and dependability.</li><li>Ability to work independently to identify problems and implement solutions. </li><li>Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.</li></ul><div><br/></div><br/><h3>Benefits</h3><br/><ul><li>Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. </li><li>Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.</li></ul>

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Clinical Research Physician - (Bilingual required - English/Spanish) Alcanza Clinical Research

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