Job Description

Exciting CRC Opportunity with large SMO! Job Duties: + Coordinate all aspects of patient involvement from study initiation until study completion. + Assist in the creation of thorough and accurate source documents during study start-up activities. + Collaborate with internal departments, sponsors, and investigators to ensure protocols are understood and assist in training staff members. + Participate in Inclusion Management (IM) and Site Initiation Visits (SIVs), communicating with sponsors and representatives. + Ensure site receives accurate information and supplies from sponsors. + Assist in reviewing participant history and confirm information with potential participants and study physicians during screening and enrolling activities. + Educate potential participants and caregivers on protocol-specific details and expectations. + Work with the physician to address questions and concerns related to the trial and informed consent process. + Maintain thorough knowledge of study-specific inclusion/exclusion criteria. + Coordinate scheduled visits, adhering to protocol visit windows and timelines. + Perform safety and efficacy assessments per protocol, including vital signs, EKGs, blood draws, and other assessments as assigned. + Collaborate with the research pharmacist to perform drug accountability and compliance at each visit and educate subjects on proper dosing regimen. + Ensure accurate and timely completion of source documents recording subject's participation in the study. + Communicate closely with all departments to ensure study visits are coordinated in compliance with protocol and GCP guidelines. + Assist investigators in the collection of information from study subjects regarding Adverse Events (AEs), concomitant medications, and other changes throughout participation. + Report study status, study-related issues, and study events to appropriate management, internal departments, and other outside agencies in a timely manner. + Responsible for subject scheduling and follow subjects through study completion, creating a follow-up care plan with the physician, study subject, and primary care provider. + Prepare and facilitate all study monitoring visits and promptly follow up with monitor follow-up letters. + Maintain professional and appropriate interactions with study subjects, caregivers, sponsors, and all other study-related personnel and staff members. + Assume other duties and responsibilities as assigned. Essential Skills + Bilingual in English and Spanish. + Proficiency in Microsoft Word and Excel. + Knowledge of medical terminology. + Effective verbal and written communication skills. Additional Skills & Qualifications + Phlebotomy skills are a plus. + Experience with interventional clinical trials. + Understanding of EKG and patient visit protocols. + Experience with PI/monitor interaction. Work Environment + The role is fully on-site from Monday to Friday, following traditional business hours from 8:00 AM to 4:30 PM. Job Type & Location This is a Permanent position based out of Hollywood, FL. Pay and Benefits The pay range for this position is $58240.00 - $76960.00/yr. Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas. Workplace Type This is a fully onsite position in Hollywood,FL. Application Deadline This position is anticipated to close on Nov 26, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Job Tags

Permanent employment, Monday to Friday,

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