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, VA, SC, TN, 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. is responsible for processing clinical research feasibilities for all sites and supporting the needs of the Business Development team. Complete feasibility in accordance with set timelines per sponsor/Clinical Research Organization (CRO) requirements.

Identify the potential investigators at sites who will be conducting the clinical research trial in conjunction with Business Development Team. Contact potential investigators/clinical site leaders to discuss study details and protocol in order to assess the feasibility of the proposed study. Maintain documentation as to sites capabilities, including lists of equipment specific to FQs (i.e.: MRI, PET, CSF, etc.).

File filled questionnaires and relevant documents into CRM. Input PI information into Sponsor, CRO and like databases on a regular basis. Assist in the management of the upcoming research trials pipeline.

Attend and successfully complete all company training programs; Maintain confidentiality of patients, customers, and company information. A high school diploma or equivalent AND 2+ years of administrative, sales support, or similar experience, OR an equivalent combination of education and experience, is required. 1+ years of clinical research experience is required. Prior experience with the feasibility process in a clinical research setting is highly preferred.

Bi-lingual (English / Spanish) proficiency is a plus. Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications,



and the ability to type proficiently (40+ wpm); Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers. Ability to work under minimal supervision, identify problems and implement solutions.

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. 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.

Alcanza Clinical

Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all. We conduct research on dozens of conditions in several therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work is important to the patients who participate, the scientists who develop these current therapies, and the entire medical community.

Because all approved medications require clinical trials, the impact of your work is exponential, reaching many thousands of future patients and improving their quality of life.

Alcanza Clinical

Research is an Equal Opportunity Employer It is the policy of the company to recruit, hire, train and promote persons in all job titles 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 category protected by law. We recognize that diversity and inclusion is a driving force in the success of our company. #

📌 Clinical Research Coordinator - Full Time (Burlington)
🏢 ActivMed Practices u0026 Research
📍 Burlington