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GENERAL SUMMARY OF POSITION:
Under the supervision of the Principal Investigator or designee, the Clinical Research Assistant is responsible for performing delegated tasks and procedures involving human subjects in support of clinical research protocols.
MAJOR RESPONSIBILITIES:
Assist PI in development of protocol-specific tools to aid in study documentationAssess eligibility of research subjects in accordance with the approved protocol and all applicable regulations including HIPAAObtain patient consent and Human Subject Committee approvals for minimal-risk studies as delegated by IRB-approved protocolCollect, record, evaluate, update, and store/transport pertinent data and samples in relation to protocolTrack study enrollment and completion of milestonesSummarize research findings and prepare presentationsPerform literature searchesSchedule patient tests and/or interviewsConduct patient telephone follow upStock, inventory, store, and order samples/supplies as needed to maintain appropriate operationsReview medical records and medical record abstractions for consistency and completenessComply with established policies, health and safety regulations and requirements, procedures, and department objectivesMaintain patient and study subject confidentialityPerform other duties as required.REQUIRED QUALIFICATIONS:
Bachelor’s degree in a scientific or health care field, or related experienceExperience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)Oral and written communication skillsExcellent organizational and interpersonal skills required.UMass Medical School RetweetedExcited to be presenting my work using to assess cost of behavioral health care in Pedi EDs at and this year. Proud to representing and
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UMass Medical School Core Competencies demonstrating the capabilities that are central across all UMMS positions that collectively contribute to UMMS success.
Freqently Asked Questions
Candidates with degrees in biology, healthcare, or related scientific fields often excel as Clinical Research Assistants in Worcester, MA. These disciplines provide foundational knowledge essential for protocol compliance, patient eligibility assessment, and accurate data handling within clinical studies.
Unlike broader research roles, Clinical Research Assistants focus on direct support to clinical trials, including enrolling patients, managing study documentation, and ensuring protocol adherence. Their tasks blend patient interaction with meticulous regulatory compliance, distinguishing them within healthcare research.
Yes, Clinical Research Assistants in Massachusetts can progress towards Clinical Research Coordinator or Associate roles by gaining hands-on experience, mastering regulatory requirements, and developing strong organizational skills, thus opening pathways to leadership in research projects.
Working at UMass Medical School entails strict adherence to HIPAA and IRB protocols, balancing meticulous data collection with patient confidentiality. The dynamic academic environment demands adaptability to evolving research priorities and interdisciplinary collaboration.
UMass Medical School offers targeted training emphasizing ethical standards, protocol compliance, and data management to ensure Clinical Research Assistants are proficient in handling human subject research with integrity and accuracy.
Clinical Research Assistants in Worcester, MA generally earn between $45,000 and $60,000 annually, reflecting regional demand, healthcare sector standards, and the specialized nature of clinical trial support roles.
Worcester's growing biotech and medical research community heightens competition for Clinical Research roles. Employers prioritize candidates with solid scientific backgrounds, regulatory knowledge, and experience with clinical protocols to meet rigorous study demands.
Public transit, carpooling, and biking are common among Worcester-based Clinical Research Assistants. The campus's accessibility supports diverse commuting choices, accommodating those balancing urban and suburban living preferences.
Strong organizational abilities, effective communication, and proficiency with data tools like Excel and Access are critical. Additionally, understanding patient consent processes and regulatory compliance elevates performance in clinical research settings.
Clinical Research Assistants at UMass collaborate closely with principal investigators, coordinators, and healthcare professionals to ensure smooth study execution, data integrity, and adherence to ethical standards, fostering a cohesive research environment.
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