Clinical Research Coordinator

Alcanza Clinical Research • Farmington Hills, MI

276d

About The Position

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX 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. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

Requirements

• A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and experience.
• Proficiency with performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc.
• BLS certified/preferred.
• Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).
• Strong organizational skills and attention to detail.
• Well-developed written and verbal communication skills.
• Well-developed interpersonal and listening skills.
• Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
• Professional, respectful of others, self-motivated, and have a strong work ethic.
• High degree of integrity and dependability.
• Ability to work under minimal supervision, identify problems and implement solutions.
• Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Nice To Haves

• Bi-lingual (English / Spanish) proficiency is a plus.

Responsibilities

• In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies.
• Screening of patients for study enrollment.
• Patient consents.
• Patient follow-up visits.
• Documenting in source clinic charts.
• Entering data in EDC and answering queries.
• Obtaining vital signs and ECGs.
• Performing basic lab procedures per protocol, such as blood specimen collection, centrifuge operation, storing and shipping of lab specimens.
• Requesting and tracking medical record requests.
• Updating and maintaining logs, chart filings.
• Maintaining & ordering study specific supplies.
• Scheduling subjects for study visits and conducting appointment reminders.
• Building/updating source as needed.
• Conducting monitoring visits and resolving issues as needed in a timely manner.
• Ensuring study related reports and patient results are reviewed by investigator in a timely manner.
• Filing SAE/Deviation reports to Sponsor and IRB as needed.
• Documenting and reporting adverse events.
• Reporting non-compliance to appropriate staff in a timely manner.
• Maintaining positive and effective communication with clients and team members.
• Practicing ALCOAC principles with all documentation.
• Assisting with study recruitment, patient enrollment, and tracking as needed.
• Maintaining confidentiality of patients, customers and company information.
• Performing all other duties as requested or assigned.
• Completing all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF.
• Preparing and attending site initiation visits (SIV's) and Investigator Meetings (IMs), as needed.
• Setting up, training and maintaining all technology needed for studies.

Benefits

• Medical, dental, vision, life insurance.
• Short and long-term disability insurance.
• Health savings accounts.
• Supplemental insurances.
• 401k plan with a safe harbor match.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree