Senior Clinical Research Coordinator

Position Summary/

Department Summary:

Under minimal guidance responsible for oversight of a portfolio of research projects. Leads the development, and implementation of clinical research projects by collaborating with Principal Investigator and/or designees to ensure targets are met on time. Develops and implements enrollment strategies and study documents including protocol, and study manuals. Provides analytical, data management, and methodological support in the development of clinical research protocols and data management tools.

Assists 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 of studies for submission.

Key Responsibilities:

* 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.

* Works with Principal Investigators and lab members to plan analyses, clean and verify data and facilitate preparation of datasets for analyses.

* May assist in writing grants. Prepare new applications for research funding and in implementation and managing ancillary study grants.

Minimum Qualifications

Education:

* A Bachelor's degree is required, Master's Degree is preferred.

Experience:

* A Bachelor's degree with 4 years of work experience is required, or an MS with 2 years of work experience

The posted pay range is Boston Children's reasonable and good-faith expectation for this pay at the time of posting.

Any base pay offer provided depends on skills, experience, education, certifications, and a variety of other job-related factors. Base pay is one part of a comprehensive benefits package that includes 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 and discounted rates on T-passes.

Experience the benefits of passion and teamwork.