Jobs · Analyst · Massachusetts

Clinical Research Coordinator

ActivMed Practices & Research, LLC. · Boston, Massachusetts, United States · 3 wk ago
AnalystFull-time

About the role

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations across AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX, and Puerto Rico. We conduct Phase I-IV studies in therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. As a Clinical Research Coordinator (CRC), you will ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.

Responsibilities

  • Screen patients for study enrollment and obtain patient consents.
  • Conduct patient follow-up visits and document in source clinic charts.
  • Enter data in EDC and respond to queries.
  • Obtain vital signs and ECGs; perform basic lab procedures per protocol (e.g., blood specimen collection, centrifuge operation, storing/shipping lab specimens, specimen accountability, and courier notification).
  • Request and track medical records; update and maintain logs and chart filings.
  • Maintain and order study-specific supplies.
  • Schedule subjects for study visits and conduct appointment reminders.
  • Build/update source documents as needed.
  • Conduct monitoring visits and resolve issues in a timely manner.
  • Ensure study-related reports and patient results are reviewed by the investigator promptly.
  • File SAE/Deviation reports to Sponsor and IRB as needed.
  • Document and report adverse events and non-compliance to appropriate staff.
  • Maintain positive and effective communication with clients and team members.
  • Adhere to ALCOAC principles in all documentation.
  • Assist with study recruitment, patient enrollment, and tracking as needed.
  • Maintain confidentiality of patients, customers, and company information.
  • Complete all activities for study start-up, including required training and uploading/printing certificates to file in ISF.
  • Prepare for and attend site initiation visits (SIVs) and Investigator Meetings (IMs) as needed.
  • Set up, train, and maintain all technology needed for studies.
  • Perform all other duties as requested or assigned.

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, is required. Proficiency with basic clinical procedures (e.g., blood pressure, vitals, EKGs, phlebotomy) is highly preferred. Bilingual (English/Spanish) proficiency is a plus.

Skills

  • Proficiency with computer applications (Microsoft Office, email, electronic health records, web applications) and typing (40+ WPM).
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Strong interpersonal and listening skills; ability to work independently and collaboratively.
  • Ability to handle multiple tasks, adapt to changing workloads, and prioritize effectively.
  • Professional, respectful, self-motivated, and 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 confidentially and in compliance with HIPAA guidelines.

Benefits

Full-time employees (30+ hours/week) are eligible for benefits starting the first day of the month following hire. Benefits include:

  • Medical, dental, and vision insurance.
  • Life insurance and short/long-term disability insurance.
  • Health savings accounts and supplemental insurances.
  • 401k plan with a safe harbor match.

About Alcanza

Alcanza Clinical Research is a national, collaborative network of clinical research sites focused on accelerating the development of new therapies by reducing barriers to participation. We conduct research on dozens of conditions across therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work impacts patients, scientists, and the broader medical community, as all approved medications require clinical trials.

Alcanza is a culturally competent organization that values diversity, inclusion, and respect. We strive to create an environment where all individuals feel welcome, heard, and respected. Our core values include being Inclusive, Impactful, Compassionate, and Determined.

Alcanza is an Equal Opportunity Employer that recruits, hires, trains, and promotes individuals without regard to race, color, religion, sex, age, national origin, marital status, veteran status, disability, sexual orientation, gender identity or expression, genetic information, or any other protected category.

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