Location: Longport,NJ, USA
Job Title: Sr. Clinical Research CoordinatorJob Description+ 5-10 years of experience coordinating Clinical Research trials+ Working to help enroll patients in clinical trials via pharmacy locations 5 days on-site.+ Must have phlebotomy proficiency+ Must have knowledge of regulatory affairs--able to work independently as the primary/sole Clinical Research professional onsite+ Excellent patient/customer service skillsManages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants).• Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol.• Creates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulations.• Contributes to the training of clinical trial staff and accountable for compliance with the operational requirements of the clinical trial.• Function as participants' primary point of contact, keeping them informed on the study progress, and facilitate involvement of other study team members, as needed (e.g., notify Principal Investigator of safety events).• Manage participant visit scheduling and technical troubleshooting, escalating issues to the appropriate individual(s).• Solicit and record information regarding safety events and preparing safety event documentation for review by the Principal Investigator.• Provides accurate and timely data collection, documentation, entry, and reporting in both Sponsor and Walgreens databases.• Supports the regulatory staff in the maintenance of regulatory documents in accordance with SOPs and applicable regulations.• Communicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participants.Hard Skills+ Clinical Research Coordinator+ Phlebotomy+ VaccineJob TypeThis is a contract position with a duration of 12 Month(s)Possibility for extension or moreAbout 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 peopleThe 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 ...@actalentservices.com ( ...@actalentservices.com) for other accommodation options.