Assistant Clinical Research Coordinator

Qualifications:

•    Meticulous, responsible, detail-oriented, able to multi-task, and solution-oriented.
•    Prior experience with consent/assenting and interviewing research subjects is a plus.
•    Have the necessary patience and resourcefulness to interact well with individuals and their families.
•    Comfortable interacting with patients/participants.
•    Able to organize and balance multiple projects at one time.

EDUCATION & EXPERIENCE (REQUIRED): 
Two years of a college degree, two years of related work experience, a bachelor’s degree in a related field, or an equivalent combination of related education and relevant experience. 

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED): 

•    Strong interpersonal skills.
•    Strong oral and written communication skills.
•    This is an onsite position.
•    Attention to detail and ability to multi-task.
•    Proficiency in technology, including Zoom, Microsoft Word, Excel, and PowerPoint.
•    Experience with research protocols and regulatory or governing bodies, which include HIPAA regulations, Institutional Review Board requirements, and Good Clinical Practices.
•    Knowledge of medical terminology.
•    Experience with RedCAP database.
•    Manual dexterity and ability to perform effectively under pressure.
•    Fluency in Spanish (optional).

CERTIFICATIONS & LICENSES: 

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred. 

PHYSICAL REQUIREMENTS*: 

•    Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
•    Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
•    Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.