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Clinical Studies Recruiter


This is a Contract position in Anaheim, CA posted June 6, 2022.

Description:The Clinical Research Recruiter is responsible for all activities related to recruitment of trial subjects:
• Database development and maintenance, preselection of suitable study candidates, organize recruitment related activities pre-, per
– and post study.
• Support clinical trials by drafting/using different recruitment related documents, perform administrative activities and act as primary contact person towards the clinical trial volunteers.
• Ensure compliance of regulatory requirements related to the protection of volunteer’s confidential data.Database Development and Maintenance:
• Responsible for development and maintenance of the NH PCRU subject recruitment capabilities to conduct a broad range of studies.
• Identify, explore and implement new methods for subject recruitment.
• Coordinate the implementation of recruitment campaigns, including the design, drafting & publication of advertisements in various media.
• Assure internal and external approvals.
• Maintain accuracy, accessibility, and confidentiality of volunteer records and reports.Recruitment and Screening Activities:
• Responsible for recruiting and orienting research activities conducted; assists in scheduling and ensuring compensation of subjects with recruitment coordinator.
• Recruit required number of subjects for studies.
• Create letters, handle text messaging, mailings or other communication methods towards subjects.
• Helps to manage subject phone calls and visits on site (as applicable).
• Responsible for the collection and documentation of electronic and written data.
• Ensure that quality, follow-up and time schedules are met.
• Respond upon all queries specific to subject data collection.
• Write and update recruitment related documents for subject use as appropriate.
• Communicate protocol requirements to study subjects and contribute to compliance.
• Demonstrate positive attitude to the subject population to ensure subject’s trust in clinical research.Skills:medical record, medical terminology, service, Customer service, edc, phlebotomy, laboratory, regulatory affairs, medical, data entry, regulatory, medical billing, medical insurance, front desk, clinical research, health care, claim, filing, microsoft office, patient records, microsoft, clinical studies, administrative supportAdditional Skills & Qualifications:At least 2 year college degree (associates) and 1 year of relevant experience, or equivalent combinationKnowledge of medical terminologyEDC (Electronic Data Capture) experience preferredFamiliarity with chart review and tracking data from charts Experience in a clinical research environment is preferred.
• Excellent written and verbal communication skills.
• Strong computer skills including competency with MS word, excel, power point.
• Ability to learn different operating systems (i.e.

• Exceptional customer service and professionalism.
• Able to demonstrate business acumen.
• Previous experience in functions involving a large element of people contact.
• Prior experience in administration and/or in healthcare environmentExperience Level:Entry Level About Actalent: Actalent connects passion with purpose.

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Actalent is an operating company of Allegis Group, the global leader in talent solutions.The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.