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, and overseeing the work of more entry level staff.

Principal Duties and Responsibilities

• 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.May be required to perform clinical tests such as phlebotomy, EKGs, etc.
• 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.
• 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, as appropriate.
• 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 an smaller area.
• Assists Principal Investigator in screening subjects for IRB approved protocols and coordinating study visits.
• All other duties as assigned.

Skills/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 professionalism and respect for subjects' rights and individual needs.

BA or BS Degree.Must have at least one year of directly related clinical research experience, and have demonstrated competence in research techniques and methodologies.Must have demonstrated an ability to work independently.

McLean is an Affirmative Action Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. 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.