Clinical Research Nurse needed in Suffolk, VA! This is a Monday to Friday opportunity. No weekends or holidays! Must have experience doing injections ! Open to non - clinical research experience! Job Description We are seeking a dedicated and professional Clinical Research Nurse to manage clinical trials in accordance with study protocols, GCP, ICH Guidelines, and SOPs. The ideal candidate will coordinate clinical trials, ensure patient safety, and maintain data integrity while adhering to regulatory requirements. Responsibilities + Coordinate assigned clinical trials including start-up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring timely data entry and query resolution, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, and providing all close-out reports. + Implement research and administrative strategies to successfully manage assigned protocols. + Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors. + Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems and resolving queries. + Maintain confidentiality of patient protected health information, sponsor confidential information, and company confidential information. + Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and SOPs. + Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner. + Ensure staff are delegated and trained appropriately and documented. + Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements. + Evaluate potential subjects for participation in clinical trials including phone and in-person pre-screens. + Execute recruitment strategies defined by the team. + Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol. + Perform clinical duties (e.g., drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope. Additional Skills & Qualifications + Bachelor’s degree and 2 years relevant experience in the life science industry OR + Associate’s degree with 4 years relevant experience in the life science industry OR + High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience + RN or LPN with an infusion certification + Phlebotomy certification if applicable and required by state law Work Environment This position is site-based and involves working in an office environment. Pay and Benefits The pay range for this position is $34.00 - $40.00 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Suffolk,VA. Application Deadline This position will be accepting applications until Jan 17, 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. 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.