Adams Clinical
Clinical Research Assistant
Boston, Massachusetts, United States
Sponsorship not specifiedDetected 8 days ago
GCPClinical TrialsClinical ResearchResearchCommunicationCollaboration
About the role
- Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions, supporting both inpatient and outpatient studies.
- Adams Clinical Site Network has locations in Watertown, MA
- Adams Clinical Site Network has locations in Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; and Dallas, TX.
Responsibilities
- Support study start-up activities, including supply inventory, document preparation, and site initiation readiness.
- Serve as a participant liaison-confirm appointments, coordinate transportation, and maintain ongoing communication.
- perform vital signs, ECGs, and specimen collection/processing as trained.
- Perform data entry into EDC systems and assist with query resolution.
- Maintain study binders, charts, and logs
- support supply management.
- Ensure accurate capture and upload of paper source documents into eSource systems in accordance with site processes and regulatory requirements, supporting long-term retention and audit readiness.
- Support CRCs during monitoring visits and assist with preparing documentation and materials to ensure audit and inspection readiness.
Requirements
- Proficiency in Microsoft Office.
- Minimum requirement of a high school diploma or GED equivalent
- training will be provided. Basic understanding of clinical research principles is a plus.
- Strong attention to detail, organization, and communication skills.
- Willingness to perform phlebotomy and clinical procedures as trained.
- Pay: $24.00 - $26.92 per hour
- Benefits:
- 401(k) matching
- Medical, Dental, & Vision insurance
- Employee assistance program
- Flexible spending account
Nice to have
- A culture of respect, transparency, and continuous improvement
- A team dedicated to improving lives through innovation and integrity
- Schedule and prepare for participant visits, including source prep, lab kits, and CRFs.
- Complete accurate, ALCOA+-compliant source documentation for delegated procedures.
- Develop proficiency in site SOPs, institutional policies, and GCP requirements to build foundational knowledge in compliant research practices.
- Assist in collecting and entering study data into trackers, logs, and EDC systems, focusing on accurate and timely data collection.
- of a high school diploma or GED equivalent
- Bachelor's degree preferred.
Compensation
- $24.00 - $26.92 per hour
Benefits
- Health savings account
- Life insurance
- Parental leave
- Obtain, track, and manage medical releases, as well as medical and pharmacy records from external providers as needed, in accordance with site SOPs and protocol requirements.
Company info
- deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare.
- Our vision is to set the gold standard for clinical trial excellence.
- We believe our people make the difference.
- Guided by our core values-Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration-we create an environment where meaningful work drives meaningful change.
- We are seeking entry-level applicants for the Clinical Research Assistant role at our Boston location.
Equal opportunity
- equal opportunity and affirmative action employer.
Visa & Work Authorization
- entation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected
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