Clinical Research Coordinator
Company: Alcanza Clinical Research
Location: Roslindale
Posted on: February 17, 2026
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Job Description:
Job Description Job Description Description 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. The Clinical Research Coordinator (CRC)
works to ensure the execution of assigned studies in compliance
with GCP, ICH, HIPAA, FDA Regulations and SOPs. Key
Responsibilities Essential Job Duties: In collaboration with other
members of the clinical research site team, works to ensure the
execution of assigned studies. Responsibilities may include but are
not limited to: Screening of patients for study enrollment; Patient
consents; Patient follow-up visits; Documenting in source clinic
charts; Entering data in EDC and answers queries; Obtaining vital
signs and ECGs; May perform basic lab procedures per protocol, such
as: blood specimen collection, centrifuge operation, storing and
shipping of lab specimens, accountability of specimens and
notification of courier for specimen pick-up; Requesting and
tracking medical record requests; Updating and maintaining logs,
chart filings; Maintaining & ordering study specific supplies;]
Scheduling subjects for study visits and conducts appointment
reminders; Building/updating source as needed; Conducting
monitoring visits and resolves 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 timely
manner; Maintaining positive and effective communication with
clients and team members; Always practicing ALCOAC principles with
all documentation; May assist with study recruitment, patient
enrollment, and tracking as needed; Maintaining confidentiality of
patients, customers and company information, and; Performing all
other duties as requested or assigned. Complete all needed
activities for study start-up, including completing required
training, uploading / printing certificates to file in ISF, etc.;
Prepare and attend site initiation visits (SIV’s) and Investigator
Meetings (IMs), as needed; May set up, train and maintain all
technology needed for studies. Skills, Knowledge and Expertise
Minimum Qualifications : 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 performing basic clinical procedures such as (blood pressure,
vitals, EKGs, phlebotomy, etc.) is highly preferred. Bi-lingual
(English / Spanish) proficiency is a plus. Required Skills:
Proficiency with computer applications such as Microsoft
applications, email, electronic health records, web applications,
and the ability to type proficiently (40 wpm); Performing basic
clinical procedures such as blood pressure, vitals, EKGs,
phlebotomy, etc Strong organizational skills and attention to
detail. Well-developed written and verbal communication skills.
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 effectively handle
multiple tasks, and adapt to changes in workloads and priorities.
Must be professional, respectful of others, self-motivated, and
have a strong work ethic. Must possess a 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. Benefits 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.
Keywords: Alcanza Clinical Research, Brockton , Clinical Research Coordinator, Healthcare , Roslindale, Massachusetts
