Job Summary:
The Clinical Research Assistant II, under the supervision of the Principal Investigator and/or senior study staff collects, processes, and enters research data in support of specified research projects. Following established protocols and procedures, they will carry out study activities and recruit and follow research subjects, as appropriate to the study objectives.
Duties and Responsibilities:
1. Collects data by review of medical records, interviews, or other means.
2. Performs coding, entry, and verification of data collected into both paper and electronic databases.
3. As appropriate to the specified position, recruits subjects into research studies and conducts follow up interviews per study protocol.
4. Assists in the processing and storage of biological specimens as needed, under supervision.
5. Observes all relevant risk management and infection control policies and procedures and any applicable quality improvement activities.
6. Collects and reviews scientific articles. Enters references into a database.
7. Prepares drafts of written documents relating to study procedures.
8. Performs general office duties including typing, photocopying, inventory, and ordering.
9. Performs other related duties as assigned.
10. Assists in preparation of IRB submissions.
11. Works evening hours and/or weekend hours as required in support of specified studies.
12. Respects and safeguards the rights of human subjects, including confidentiality of information gathered.
13. Observes all general hospital policies, guiding principles, rules, and regulations, and consistently adheres to the Care New England service standards.
Requirements:
Bachelor's degree required
Basic computer skills, e.g. familiarity with Microsoft software, completing spreadsheet/data entry.
Ability to work with diverse populations and support an inclusive, culturally responsive environment.
Additional Information:
EEOC Statement: Care New England is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Freqently Asked Questions
North Smithfield's medical research sector is growing, but Clinical Research Assistant II positions remain moderately competitive due to a limited number of specialized healthcare institutions. Candidates with hands-on experience in data collection and protocol adherence often have an advantage in this Rhode Island locale.
While a bachelor's degree is essential, familiarity with IRB submissions and proficiency in Microsoft Office suites can boost employability in Rhode Island. Employers like Care New England value candidates who can navigate clinical databases and maintain compliance with local research regulations.
Mastering accurate data entry, ethical handling of human subject information, and understanding biological specimen processing are key. Strengthening communication skills for subject recruitment and follow-up interviews also enhances effectiveness in this role.
Absolutely, starting as a Clinical Research Assistant II offers valuable exposure to study protocols and data management, laying groundwork for promotions into Clinical Research Coordinator or Associate roles, especially with continued education and certification.
Daily duties include reviewing patient records, entering and verifying research data, assisting with specimen handling, and preparing documentation for study protocols. Flexibility for evening or weekend hours is often required to support ongoing trials.
Care New England emphasizes adherence to strict service standards and inclusivity, fostering a culturally responsive environment. Their research assistants often engage in broader tasks, including IRB submissions and quality improvement initiatives, reflecting a comprehensive support structure.
Salaries typically range from $45,000 to $55,000 annually, reflecting local healthcare market trends and role responsibilities. Experience with data management and protocol compliance can influence compensation levels within this bracket.
Care New England supports skill development through supervised training under principal investigators and senior staff, ensuring assistants gain practical knowledge in research protocols, data handling, and regulatory compliance within a supportive environment.
By meticulously collecting and verifying data, facilitating subject recruitment, and assisting with specimen processing, this role ensures high-quality inputs that are critical for reliable study outcomes and advancements in clinical research.
Balancing rigorous protocol adherence with diverse patient populations in a smaller community presents challenges. The role demands cultural sensitivity and adaptability, especially during off-hours work supporting various study schedules.
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