CrawlJobs Logo

Senior Clinical Research Coordinator

United States, Brookline 58676.80 - 93901.60 USD / Year · Job Posted January 29, 2026
Apply Position
Job Link Share

Job Description

At Boston Children’s Hospital, the quality of our care – and our inclusive hospital working environment – lies in the diversity of our people. With patients from local communities and 160 countries around the world, we’re committed to reflecting the spectrum of their cultures, while opening doors of opportunity for our team. Here, different talents pursue common goals. Voices are heard and ideas are shared. Join us, and discover how your unique contributions can change lives. Yours included. The Rosamund Stone Zander and Hansjoerg Wyss Translational Neuroscience Center (TNC) is seeking a dynamic and innovative Senior Clinical Research Coordinator to join our team. The TNC strives to improve the lives of all children with neurodevelopmental disorders by fostering timely and efficient translational research. The Sr. Clinical Research Coordinator will collaborate with Principal Investigators and study stakeholders to manage the daily operations of research studies and will develop and oversee the implementation of best practice guidelines for conducting various research protocols. The Sr. Clinical Research Coordinator will contribute to the development of budgets and monitor study finances, oversee maintenance of research equipment, and ensure compliance with hospital and governmental regulations. The Sr. Clinical Research Coordinator will identify and manage operational, logistical, and regulatory challenges related to the conduct of clinical trials and act as a leader in overseeing their resolution. The Sr. Clinical Research Coordinator will manage and train research staff and conduct the Performance Management process.

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
  • Presents and prepares training materials as part of the sponsored educational efforts
  • Provides analytical, data management, and methodological support to Principal Investigator and/or designees in the development of clinical research protocols and data management tools
  • Manages data for single and/or multi-institutional investigations
  • Develops study-specific data management and quality assurance procedures and monitors their implementation at site visits and/or periodic review of study data management reports

Requirements

  • BA/BS degree in health, psychology or a related field is required
  • Master’s Degree is preferred
  • Bachelor’s Degree with 4 years of relevant work experience
  • OR Master’s Degree and 2 years of relevant work experience
  • Knowledge of clinical research processes and best practices
  • Exceptional organizational skills and multi-tasking abilities, with good attention to detail
  • The ability to take initiative and work with minimal direct supervision
  • Ability to work collaboratively with multi-disciplinary project teams
  • Ability to communicate effectively both orally and in writing

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

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Senior Clinical Research Coordinator

8 matching positions

Senior Clinical Research Coordinator

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...
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 required, Master's preferred
  • Bachelor's Degree with 4 years of relevant work experience required OR Master's Degree and 2 years of relevant work experience required
  • Prior clinical trial coordination experience required
Job Responsibility
Job Responsibility
  • Oversee daily study operations
  • Manage regulatory compliance
  • Coordinate team tasks
  • Coordinate budgets and invoicing
  • Consent patients
  • Schedule trial visits and coordinate participant travel
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

Senior Clinical Research Coordinator

At Boston Children’s Hospital, the quality of our care – and our inclusive hospi...
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 is required
  • Master’s or a higher level degree is preferred
  • Bachelor’s with 4 years of relevant work experience
  • OR Master’s level degree and 2 years of relevant work experience is required
  • Applicants with medical degrees are strongly encouraged to apply
  • Experience in advanced analytics or programming (R, Python) is preferred, though not required
  • Strong writing skills to assist with grants and manuscripts
Job Responsibility
Job Responsibility
  • Oversight of a portfolio of research projects
  • Lead the development and implementation of clinical research projects
  • Develop and implement enrollment strategies and study documents including protocol, and study manuals
  • Provide analytical, data management, and methodological support in the development of clinical research protocols and data management tools
  • Assist with the development and implementation of best practice guidelines for conducting various clinical research protocols
  • May train lab staff members and assist in writing articles and papers for submission
  • In conjunction with the PIs and/or designees designs, develops, and implement clinical research projects such as enrollment strategies, study materials, and study documents
  • Assist in writing grants
  • Prepare new applications for research funding and implementing and managing ancillary study grants
  • Responsible for daily operations of the study
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

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

Senior Clinical Research Associate

Location
Location
Canada , Alberta; Vancouver; Burlington
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
  • Excellent written and verbal communication in English
  • Experience monitoring Oncology studies
  • Good social skills enabling you to deal with queries in a timely manner
  • Willingness to travel as required (approximately 60%)
Job Responsibility
Job Responsibility
  • Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
  • Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
  • you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
  • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
  • Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements
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
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

Senior Clinical Research Associate - Home-Based (CANADA). ICON plc is a world-le...
Location
Location
Canada , Montreal; Toronto; Vancouver; Burlington; British Columbia; New Brunswick; Quebec
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
  • 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role
  • 3+ years is required for a level 3
  • Ability to travel 70%
  • Knowledge of ICH and local regulatory authority regulations regarding drug trials
  • Applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status
Job Responsibility
Job Responsibility
  • Monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements
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
  • Fulltime
Read More
Arrow Right

Contract Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
United States , Los Angeles
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
  • Minimum of 3 years independent monitoring
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication skills, with attention to detail
  • Ability to work independently and collaboratively in a fast-paced environment
  • Ability to travel at least 80% of the time (international and domestic - fly and drive) and should possess a valid driver's license
Job Responsibility
Job Responsibility
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
  • Collaborating with investigators and site staff to facilitate smooth study conduct
  • Performing data review and resolution of queries to maintain high-quality clinical data
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports
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
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

Senior Clinical Research Associate - France - Remote. ICON plc is a world-leadin...
Location
Location
France , Paris; Lyon; Montpellier
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum 3 years' experience independent external monitoring of commercial studies within CRO or Pharma/Biotech companies
  • Minimum 3 years' experience as a CRA within the pharmaceutical/Biotech companies or a CRO
  • Excellent organization skills
  • Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
  • Strong IT skills
  • Strong communication with the ability to multitask and work effectively under pressure
  • Fluency in French and professional proficiency in English
Job Responsibility
Job Responsibility
  • Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
  • Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
  • Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
  • Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
  • Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines
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
  • Fulltime
Read More
Arrow Right

Senior Clinical Research Associate

Clinical Research Associate. ICON plc is a world-leading healthcare intelligence...
Location
Location
Norway
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • University degree in medicine, science, or equivalent
  • Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
  • Excellent written and verbal communication in Norwegian and English
  • Good social skills enabling you to deal with queries in a timely manner
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
  • Located in the Greater Oslo region
Job Responsibility
Job Responsibility
  • Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
  • Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
  • you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
  • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
  • Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements
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