Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR (openings in various states as well : (MD, VA, GA, IN, TX) Required: 2+ years of experience as a Clinical Research Coordinator Experience with oncology protocols preferred Responsibilities: Responsible for the overall successful implementation and ongoing site management of the research studies. Actively recruits and screens eligible patients for research protocols as assigned. Assists and conducts Informed Consent process. Coordinates and implements enrollment and follow-up procedures to collect, data from patient charts, medical records, questionnaires, and other sources. Performs all study lab processing and shipping as assigned. Completes Case Report Forms/Source Templates and pertinent study-related forms accurately and within specified time limits. Maintains contact with study patients to facilitate study retention and their care, including communication regarding study requirements, coordinates drug dispensing, and other procedures, treatment, etc. Benefits: Medical, Dental & Vision Plans 401k Paid Holiday & Vacations Employee Assistance Program Corporate discounts and much more. Contact Us: Please email a copy of your resume and 2-3 professional references to 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. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people 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 process due to a disability, please email for other accommodation options.