Clinical Research Assistant Position Available In Palm Beach, Florida
Tallo's Job Summary: The Research Assistant position at Headlands Research in Lake Worth, FL, offers a full-time role with an estimated salary range of $35.4K - $41.8K a year. The role involves assisting in clinical research protocols by collecting clinical data, setting up ediaries, screening and enrolling study subjects, and verifying study documents. Qualifications include clinical research and laboratory experience, knowledge of medical terminology, and proficiency in Microsoft Office, particularly Excel.
Job Description
Clinical Research Assistant Headlands Research – 2.3
Lake Worth, FL Job Details Full-time Estimated:
$35.4K – $41.8K a year 10 hours ago Qualifications Microsoft Excel Clinical research Laboratory experience Microsoft Office Clinical trials Medical terminology Documentation review Communication skills Entry level
Full Job Description Overview:
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. This Research Assistant role is full-time and will be based onsite in Lake Worth, FL. You can read more about us at headlandsresearch.com . The Role JEM Research Institute, a Headlands Research site, is looking for a Research Assistant to assist coordinators in clinical research protocols. This individual will work directly with the coordinators, investigators, and other research staff to ensure protocol visits are being completed in accordance with protocol guidelines.
Responsibilities:
To assist research coordinators in conducting clinical trials. Responsibilities include but are not limited to: Collect clinical data: vital signs, telephone calls and entering data into electronic data system, setting up ediaries and training subjects on completion of ediaries, monitor subject diary entries and follow up to ensure completion, posting subject payments, Screening and enrolling study subjects based on inclusion/exclusion criteria Verifying study documents
Qualifications:
Clinical research experience preferred Knowledge in medical terminology and laboratory skills preferred Knowledge with Microsoft office required (especially Excel) Excellent interpersonal and communication skills—interact effectively with professional, administrative staff, sponsor and regulatory representatives, patients, potential subjects, and referral sources Accuracy, attention to detail and ability to set priorities and meet deadlines Be Proactive/Think outside the Box
