CrawlJobs Logo

Clinical Research Assistant

childrenshospital.org Logo

Boston Children's Hospital

Location Icon

Location:
United States , Brookline

Category Icon
Category:
Research and Development

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

41246.40 - 61339.20 USD / Year
Save Job
Save Icon
Apply Position

Job Description:

The Biobehavioral Research Laboratory in the Department of Psychiatry is currently conducting a longitudinal study to understand risk factors for the development of anxiety and other challenges in youth. This longitudinal project involves assessments from infancy through early adolescence on neural, physiological, environmental, and behavioral predictors and markers of anxiety in typically developing children. Current study activities focus on follow-up assessments of participants at ages 11 and 13 years of age.

Job Responsibility:

  • Consent and schedule participants for research studies through written communication and video conferencing platforms
  • Provide detailed background information regarding the study to families, communicate all policies and procedures, and respond to all inquiries
  • Execute in-person study visits with participants following established research protocols
  • Measures include eye tracking, electroencephalography (EEG), physiology, and questionnaires
  • Work with a team of coordinators and RAs on data collection, data entry, and informed consent procedures, and participate in quality control efforts
  • Conduct database maintenance, data processing, and analyses
  • Assist Principal Investigator in planning and implementing research studies and perform other miscellaneous administrative duties as assigned or required

Requirements:

  • Bachelor’s Degree in psychology, child development, cognitive science, neuroscience, or related field required
  • Experience working with youth in a research setting, preferably using physiological, behavioral, and/or neuroimaging measures, such as eye tracking, heart rate, EEG, or ERP
  • Flexible schedule, including some evenings and weekends
  • Excellent written and verbal communication skills
  • High attention to detail and organizational skills, ability to multitask, and analytical skills to gather and interpret data
  • Well-developed interpersonal skills in order to interact with participants and families and work collaboratively on a team

Nice to have:

Advanced computer skills, such as knowledge of SPSS/R/Python or similar programs

What we offer:
  • flexible schedules
  • affordable health, vision and dental insurance
  • child care and student loan subsidies
  • generous levels of time off
  • 403(b) Retirement Savings plan
  • Pension
  • Tuition and certain License and Certification Reimbursement
  • cell phone plan discounts
  • discounted rates on T-passes

Additional Information:

Job Posted:
May 05, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
Icon
Boston Children's Hospital - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Clinical Research Assistant

Senior Clinical Research Coordinator

The Computational Health Informatics Program (CHIP) is seeking an experienced, h...
Location
Location
United States , Boston
Salary
Salary:
58676.80 - 93901.60 USD / Year
childrenshospital.org Logo
Boston Children's Hospital
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree
  • Master’s preferred
  • Bachelor’s degree and 4 years of relevant work experience OR Master’s degree and 2 years of relevant work experience
  • Analytical skills to gather and interpret data in which the information or problems are moderately complex to complex
  • Well-developed communication skills to provide critical information to patients, effectively deal with conflicting views or issues, and the ability to mediate fair solutions
  • Ability to effectively engage with and influence others
  • build working relationships and can work independently and as a team member, leads others when needed
  • Act as a resource and must be knowledgeable and compliant in all hospital, State, and Federal regulatory requirements, including hospital policy and procedures
Job Responsibility
Job Responsibility
  • In conjunction with the Principal Investigator and/or designees designs, develops, and implement clinical research projects such as enrollment strategies, study materials, and study documents
  • Responsible for daily operations of the study
  • Develops and implements processes and procedures to meet study goals and protocol requirements
  • Participate in training and prepare study related training materials
  • Plans and prioritizes the work of administrative and support personnel on all clinical study activities
  • Consents and enrolls patients for research studies by providing detailed information on the Clinical Study to patients and families
  • Communicates all policies and procedures and responds to all inquiries
  • Evaluate the suitability of prospective study candidates and make selections based on clinical knowledge of each study
  • Provide input for updates of SOPs and drafting of new quality documentation
  • Assist with developing and implementing best practice guidelines for conducting various clinical research protocols
What we offer
What we offer
  • flexible schedules
  • affordable health, vision and dental insurance
  • child care and student loan subsidies
  • generous levels of time off
  • 403(b) Retirement Savings plan
  • Pension
  • Tuition and certain License and Certification Reimbursement
  • cell phone plan discounts
  • discounted rates on T-passes
  • Fulltime
Read More
Arrow Right

Call Center Agent – Clinical Research

A confidential clinical research organization is urgently hiring a Call Center A...
Location
Location
United States , Baltimore
Salary
Salary:
22.00 - 26.00 USD / Hour
revelstaffing.com Logo
Revel Staffing
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High School Diploma or GED required
  • Bachelor’s degree preferred
  • Minimum 2 years of call center, customer service, or clinical research–related work experience
  • MediClear Certification (or equivalent healthcare compliance credential) required
  • Strong written and verbal communication skills, with the ability to manage a fast-paced call queue
  • Proficiency with computer systems, call distribution tools (such as Cisco Enterprise Contact Center), and data entry software
  • Demonstrated ability to stay organized and maintain accuracy in a high-volume, metric-driven environment
Job Responsibility
Job Responsibility
  • Volunteer Recruitment & Coordination: Handle high-volume inbound and outbound calls and emails to recruit participants for clinical research studies
  • Follow study-specific telephone scripts to pre-screen potential volunteers and explain eligibility requirements
  • Schedule screening appointments and accurately enter participant data into the volunteer database (ClinBase™ or equivalent)
  • Track and report recruitment progress, escalating efforts as needed to meet enrollment goals
  • Compliance & Documentation: Review clinical trial protocols and assist in creating recruitment documents (scripts, study fact sheets, call strategies)
  • Maintain strict confidentiality of participant information in alignment with HIPAA, and Good Clinical Practices (GCP)
  • Accurately log all communications and update participant records in real time
  • Team Collaboration: Participate in daily team meetings to provide updates on recruitment status
  • Communicate openly with screening teams and management to coordinate appointment times and recruitment strategies
  • Assist in performance reviews and contribute to a positive, results-oriented team environment
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...
Location
Location
United States
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent attention to detail
  • Good written and verbal communication skills
  • Good collaboration and interpersonal skills
  • Good negotiation skills
  • Proficient in written and spoken English language required
  • Fluency in local language(s) required
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
  • Good knowledge of relevant local regulations
  • Good medical knowledge and ability to learn relevant Client Therapeutic Areas
  • Basic understanding of the drug development process
Job Responsibility
Job Responsibility
  • Contributes to the selection of potential investigators
  • In some countries, as required, accountable for study start-up and regulatory maintenance
  • Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles
  • Confirms that site staff have completed and documented the required training appropriately
  • Actively participates in Local Study Team (LST) meetings
  • Contributes to National Investigators meetings, as applicable
  • Initiates, monitors, and closes study sites in compliance with Client Procedural Documents
  • Shares information on patient recruitment and study site progress
  • Drives performance at the sites
  • Proactively identifies and ensures timely resolution to study-related issues
What we offer
What we offer
  • Patient-focused in everything we do
  • Supportive and inclusive environment
  • Career growth and development
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Campus Director, Clinical Education - Physician Assistant

The Campus Director of Clinical Education, Physician Assistant is a key member o...
Location
Location
United States , Ontario
Salary
Salary:
138230.12 - 200406.07 USD / Year
americancareercollege.edu Logo
American Career College
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • For PA and Physician Candidates: Minimum of three (3) years of teaching, research, or clinical experience in a PA program/Medical School, or equivalent*** experience in health professions education, healthcare delivery, or related fields that directly support PA student learning and curricular outcomes.
  • For Non-Clinician Scientist candidates: Minimum of one (1) year of full-time experience in PA education, academic support, or curriculum development in alignment with program needs.
  • Demonstrated the ability to develop clinical and didactic curriculum, program evaluation and student assessment.
  • Leadership knowledge in the program field to cultivate a learner-centered environment and to foster excellence.
  • Knowledge and evidence of strong supervisory and management skills as applicable to specialized program area.
  • Knowledge of state, federal and local laws/regulations relating to programs, governmental compliance and other regulatory standards such as Title IV, WSCUC, and ARC-PA and other accreditation standards.
  • Physician Assistant/Associate (PA) Candidates: Graduation from an ARC-PA accredited PA program.
  • Master’s degree in education or a related health- or social-science discipline.
  • Current National Commission on Certification of Physician Assistants (NCCPA) certification or eligibility* to sit for the PANCE (initial certification) or PANRE (recertification) at the time of hire.
  • State PA licensure or eligibility* for licensure in state of campus location.
Job Responsibility
Job Responsibility
  • Collaborate as a member of the programmatic leadership team, which may consist of the MPA Dean/Program Director, Medical Director, Director of Academic Education, and Director of Student Success to achieve a shared vision for the program.
  • Collaborate with the MPA Dean/Program Director, Medical Director, and the WCU Clinical Operations team to develop, evaluate, and maintain clinical sites and preceptors sufficient in number and quality to meet ARC-PA Standards.
  • Communicate with MPA Dean/Program Director ongoing new site development and needed support to facilitate Program/Preceptor relationships, including support from the Medical Director.
  • Contacts, develops new and maintains established clinical affiliations, assuring all clinical sites meet the program’s prescribed learning outcomes, and securing appropriate contact and specific contractual agreement information including identified preceptors, number and types of placements, renewals, insurance and liability matters, and other pertinent issues important to seamless transition of students to clinical sites.
  • Prepares and submits to MPA Dean/Program Director annual program clinical calendar, individual student clinical placement schedule, and oversees preparation and formal distribution of student clinical placement assignments with detailed site, setting, and discipline-related information on timeline set by MPA Dean/Program Director.
  • Provide leadership, oversight, and performance evaluation for the clinical phase team, as assigned.
  • Develops, maintains, and conducts a schedule for clinical site visitation and presents a written copy to the MPA Dean/Program Director at a specified time each year with updated list of new and renewed affiliation agreements.
  • Develops, implements, stores, and updates as needed Clinical Site Visit Forms to ensure rapid retrieval and MPA Dean/Program Director and faculty access to documented site visits and/or phone calls.
  • Conduct clinical site visits and monitor student performance in Supervised Clinical Practice Experiences (SCPEs).
  • Lead the design, development, implementation, coordination and ongoing evaluation of an innovative clinical curriculum to ensure alignment with ARC-PA Standards, PAEA’s End-of-Rotation Exams, the NCCPA blueprint, and degree requirements.
What we offer
What we offer
  • medical
  • dental
  • vision
  • flexible spending accounts
  • 401(k) match
  • paid time off
  • holidays
  • parental leave
  • tuition reimbursement
  • adoption assistance
  • Fulltime
Read More
Arrow Right

Medical Research Associate

Medical Research Associate (Phlebotomist/Medical Assistant)- ICON San Antonio TX...
Location
Location
United States , San Antonio
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High School Diploma or equivalency with medical assistant training/certification or other allied health certification
  • Medical Assistant, Phlebotomy Technician, Paramedic, EMT, OR LVN preferably with two years of experience
  • Strong organizational and time management skills, with attention to detail in data collection and documentation
  • Proficiency with research software and tools for data entry, analysis, and reporting
  • Excellent communication and teamwork skills, with the ability to work collaboratively with researchers and other stakeholders
Job Responsibility
Job Responsibility
  • Assisting in the planning and execution of clinical trials and research studies, including data collection and management
  • Supporting the research team with literature reviews, data entry, and analysis to inform study protocols and findings
  • Maintaining accurate and organized research documentation, ensuring compliance with regulatory and ethical standards
  • Collaborating with cross-functional teams to ensure timely completion of research tasks and adherence to study timelines
  • Assisting with the preparation of research reports, manuscripts, and presentations for internal and external stakeholders
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Parttime
Read More
Arrow Right

Clinical Research Coordinator II-OB/GYN

Under minimal supervision, coordinates the clinical assessments of the study sub...
Location
Location
United States , New York
Salary
Salary:
63653.84 - 85000.06 USD / Year
mountsinai.org Logo
Mount Sinai Health System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelors degree in sciences or related field
  • 2 years of clinical research
Job Responsibility
Job Responsibility
  • Analyzes moderately complex clinical research data
  • Assists in interpreting clinical research data
  • Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects
  • Prepares and ensures grant applications, IRB/GCO documents are submitted
  • Ensures accurate and complete compilation of subject data through chart reviews
  • Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials
  • Obtains informed consent under supervision of the Principal Investigator, Clinical Research Manager, or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects, and for studies involving genetic tests
  • Independently obtains informed consent for other clinical studies
  • Mentors Clinical Research Coordinators in training
  • Performs other related duties
Read More
Arrow Right

Clinical Trial Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
South Korea , Seoul
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or healthcare-related field
  • Prior experience or strong interest in clinical research
  • Knowledge of clinical trial processes, regulations, and guidelines
  • Excellent organizational and communication skills
  • Ability to work collaboratively in a fast-paced environment with attention to detail
  • Customs Clearance : Mandatory requirement
Job Responsibility
Job Responsibility
  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements
  • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions
  • Support the preparation of study-related materials, such as informed consent forms and case report forms
  • Work with cross-functional teams to facilitate communication and ensure smooth trial execution
  • Contribute to the tracking and reporting of clinical trial metrics and milestones
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Pharmacovigilance Assistant

We are currently seeking an Administrative Assistant to join our diverse and dyn...
Location
Location
Poland; Bulgaria , Warsaw; Sofia
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in life sciences, pharmacy, or a related field or equivalent experience in an administrative role (any industry)
  • Basic understanding of pharmacovigilance principles and regulatory requirements is advantageous but not essential
  • Strong attention to detail and organizational skills, with the ability to manage multiple tasks efficiently
  • Effective communication and collaboration skills, with a focus on maintaining accuracy in documentation and reporting
  • Ability to work in a fast-paced, regulated environment, ensuring compliance with safety guidelines and protocols
  • Excellent computer skills (Microsoft Word, Excel, Outlook, PowerPoint)
  • Fluent in written and verbal English
  • Ability to work effectively independently and within a team environment and across global teams
Job Responsibility
Job Responsibility
  • Complete all departmental project activities accurately in accordance with ICON SOPs, Project Specific Procedures, regulatory requirements, and Sponsors processes
  • Provide administrative support to project teams as required
  • Distribute reports to Sponsors, sites, and applicable ICON personnel
  • Coordinate setup of required systems and mailboxes during study startup
  • File all documents within allotted timeframes, including maintenance of project mailboxes and maintenance of TMF and E-TMF
  • Maintain data entry for safety event and miscellaneous tracking logs for all current projects
  • Assist with organization and planning of meetings
  • Daily entry into, and maintenance of, appropriate tracking systems
  • Maintain project training records for all assigned project team members
  • Handle Safety Reporting courier submissions to Competent Authorities and Ethics Committees
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme, LifeWorks
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments
  • Fulltime
Read More
Arrow Right