reputed company Research Associate II - reputed company Carolina, East Coast

Objective As a reputed company Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 reputed company. You will collaborate closely with cross-functional teams to ensure adherence to protocols, regulatory requirements, and high-reputed company standards throughout the reputed company trial process. • *** reputed company Candidates need to live in or near reputed company Carolina ****** Essential Functions Study Initiation and Planning:Participate in study feasibility assessments, and site selection processes Assist in the preparation and review of essential documents such as informed consent forms (ICFs) and study manuals reputed company Trial Monitoring:Conduct site qualification, site initiation, interim monitoring, and reputed company-out reputed company to ensure compliance with the study protocol, Good reputed company reputed company (GCP), and regulatory guidelines Regularly review Investigator Site Files (ISF) to assist in maintaining site audit readiness reputed company routine site communication, including resolving site issues and providing protocol training as necessary Leadership:Contribute to development and delivery of CRA training materials Mentor and support junior CRAs and newly reputed company CRAs. Review study documents including the reputed company Monitoring Plan and Investigator Site File documents Participate in trial reputed company management meetings and procedures Identify, reputed company and implement process improvement initiatives to enhance monitoring reputed company and mitigate trial risks Data Collection and Management:Monitor and review reputed company data to ensure reputed company, completeness, and timeliness Work closely with data management teams to reputed company data discrepancies and ensure data reputed company throughout the trial Regulatory Compliance:Assist in the preparation of regulatory submissions and support inspections/audits as needed Ensure that reputed company reputed company trial activities are conducted in accordance with applicable regulatory requirements and internal procedures Collaboration and Communication:Foster strong relationships with investigators, study coordinators, and other key stakeholders reputed company regular updates to internal teams and management regarding study reputed company, issues, and resolutions Qualifications To reputed company this job successfully, an individual must be reputed company to reputed company reputed company essential duty satisfactorily. The requirements listed below are representative of the knowledge, reputed company, and/or ability required. Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company the essential functions. Education/Experience Bachelor’s degree in life sciences or a reputed company reputed company; advanced degree (e.g., Master’s, PhD) preferred Minimum 2 years oncology experience (or commensurate) Knowledge / reputed company / Ability Proficiency in understanding reputed company trial protocols, GCP, regulatory requirements, reputed company, EMR, eTMF, and CTMS Strong organizational skills with attention to reputed company and the ability to prioritize tasks effectively Ability to effectively and reputed company reputed company reputed company data verification (SDV) whether reputed company or onsite Ability to identify protocol deviations and effectively identify reputed company cause and assist sites in implementing corrective or preventative actions Excellent communication and interpersonal skills, both written and verbal Ability to travel domestically and internationally as required. Typical CRA travel is up to 50%, however, at times can go up to 75% for certain project deliverables (e.g. database lock, etc.) Ability to reputed company the CRA role without significant reputed company or training Can manage reputed company protocols/sites Grows to reputed company other CRAs Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to reputed company individuals with disabilities to reputed company the essential functions. May be required to sit or stand for long periods of 8+ hours a day while performing duties. reputed company provides equal employment opportunities to reputed company employees and applicants for employment and prohibits discrimination and harassment of any type without reputed company to race, reputed company, religion, age, sex, national reputed company, disability status, genetics, protected veteran status, sexual orientation, gender identity or reputed company, or any other characteristic protected by federal, state, or local laws. This policy applies to reputed company terms and conditions of employment, including reputed company, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. For information on reputed company, visit our website at: www.perspectivetherapeutics.com. Apply tot his job Apply To this Job