Clinical Research Assistant II

McLean Hospital; Belmont (MA); On-site; USD 67,653,000 - 101,120,000; Full time

Job summary

McLean Hospital seeks a Clinical Research Coordinator to support sponsored clinical studies. You will coordinate participant screening, recruitment, data management, and protocol development under the guidance of the Principal Investigator.

You will maintain study databases, ensure data validation and quality control, assist with analyses, train new staff, and may supervise a small team as needed. Onsite position at 115 Mill Street.

Qualifications

• Bachelor's degree required.
• Minimum of 1 year of directly related clinical research experience.

Responsibilities

• Coordinate implementation of sponsored clinical research studies.
• Initiate and maintain contact with study participants.
• Screen applicants for eligibility and determine suitability.
• Develop and implement patient recruitment strategies with PI input.
• Develop, organize, and maintain the study database.
• Perform data validation and quality control.
• Assist with preliminary analyses and liaise with statistical consultant.
• Contribute to protocol development and IRB submissions.
• Train and orient new staff; may supervise a small team.

Skills

Computer literacy

Independent work

Interpersonal skills

Communication skills

Analytical skills

Clinical research protocols

Organizational skills

Respect for subjects

Teamwork

Education

Bachelor's Degree

Job description

Site: The McLean Hospital Corporation

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.

Job Summary

Summary
Working independently and under very general supervision, provides support to clinical research studies. May be responsible for the following activities: making independent judgment of suitability of potential participants for clinical trials, developing and implementing patient recruitment strategies, recommending changes to protocols, managing existing datasets, and overseeing the work of more entry level staff.

Does this position require Patient Care?
No

Essential Functions

• Coordinates the implementation, both internally and externally, of sponsored clinical research studies.
• Initiates and maintains contact with study participants.
• Responsible for screening applicants, ensuring they meet appropriate criteria, and makes independent judgment as to the suitability of their participation.
• Working in concern with the Principal Investigator, develops and implements patient recruitment strategies.
• Develops, organizes, and/or maintains the study database.
• Responsible for data validation and quality control.
• May also conduct preliminary analyses and assist the lab's statistical consultant.
• In conjunction with the Principal Investigator, develops and implements new research protocols including design, data collection systems and institutional review board approval.
• Recommends changes to research protocols.
• Performs literature searches to support protocol development for new studies and the interpretation of existing datasets.
• Assists Principal Investigator with preparation for presentation and written published articles.
• Trains and orients new staff.
• May serve as a team leader or in a supervisory capacity in a smaller area.
• Assists Principal Investigator in screening subjects for IRB approved protocols and coordinating study visits.

Qualifications

Education
Bachelor's Degree required

Can this role accept experience in lieu of a degree?
No

Licenses and Credentials

Experience
Must have at least one year of directly related clinical research experience, and have demonstrated competence in research techniques and methodologies. 1-2 years required

Knowledge, Skills and Abilities

• High degree of computer literacy; knowledge of data management programs.
• Ability to work independently.
• Excellent interpersonal skills are required for working with the study participants.
• Good oral and written communication skills; careful attention to detail.
• Analytical skills and the ability to resolve technical or research problems and issues and to interpret the acceptability of data results.
• Knowledge of clinical research protocols.
• Excellent organizational skills and ability to prioritize a variety of tasks.
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs.
• Must be able to consistently demonstrate McLean Values of integrity, compassion and respect, diversity and teamwork, excellence and innovation in their work activities and interactions.
• Must have demonstrated an ability to work independently.

Additional Job Details (if applicable)

Remote Type

Onsite

Work Location

115 Mill Street

Scheduled Weekly Hours

20

Employee Type

Regular

Work Shift

Day (United States of America)

Pay Range

$23.61 - $35.29/Hourly

Grade

MRA501At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth.

EEO Statement:

1600 The McLean Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.

At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.