Clinical Research Coordinator II - Lowell General Hospital, Cancer Center - On-Site

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* Hours:

** 32 hours weekly, 4 days. Flexible with schedule of 7am-330pm or 830am-5pm during weekdays.
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* Location:

** Lowell General Hospital - Main Campus. On-site.
** Job Profile Summary
** In addition, this role focuses on performing the following Research Programs and Projects duties:
Supports the development of new products and innovation.  Includes Clinical roles focused on research projects.  Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. A professional individual contributor role that may direct the work of other lower level professionals or manage processes and programs.  The majority of time is spent overseeing the design, implementation or delivery of processes, programs and policies using specialized knowledge and skills typically acquired through advanced education.
An entry level role that applies broad theoretical job knowledge typically obtained through advanced education.  May require the following proficiency:  work is closely supervised, problems faced are not typically difficult or complex, and explains facts, policies and practices related to job area. This role focuses on performing work related to research and development of new products, innovation, and improvement of products and processes.  

This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned.
** Job Description
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* Minimum Qualifications:

** 1. Bachelor’s degree OR High School Diploma or equivalent
** AND
* * Four (4) years of related experience.
2. Basic Life Support (BLS) certification may be required based on specific role requirements.
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* Preferred Qualifications:

** 2. Previous experience in clinical trials.
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* Duties and Responsibilities:

** The duties and responsibilities listed below are intended to describe the general nature of work and are not intended to be an all-inclusive list.  Other duties and responsibilities may be assigned.
6. Responsible for assisting with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review, adverse event reporting and annual reviews.
8. Maintains patient confidentiality per HIPAA regulations and keeps study information in a safe and secure location. Adheres to FDA Good Clinical Practice Guidelines.
10. Arranges necessary tests and procedures in accordance with protocol requirements and reports results to the investigator.
14. Assesses potential patients and eligibility for inclusion in a particular protocol based on protocol requirements.
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* Physical Requirements:

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* ** Skills & Abilities:
** 1. High degree of organizational talents, data collection and analysis skills.
3. Excellent computer skills including word processing.
4. Ability to prioritize quickly and appropriately.
5. Excellent communication and interpersonal skills.

Tufts Medicine is a leading integrated health system bringing together the best of academic and community health care to deliver exceptional, connected and accessible care experiences to consumers across Massachusetts. Comprised of Tufts Medical Center, Lowell General Hospital, Melrose Wakefield Healthcare, an expansive home care network and a large clinically integrated physician network, Tufts Medicine has more than 15,000 dedicated employees and caregivers.

The health system came together in 2014 to leverage the experience of its member organizations and integrate their missions to together transform the ways that consumers engage with and experience their care.
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