CRA II - Sponsor Dedicated (Home-Based - FL / GA)

CRA II - Sponsor Dedicated (Home-Based - FL / GA) Updated: Yesterday Location: USA-GA-Remote Job ID: 25108402 Description Syneos Health® is a leading fully‑integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. Job Responsibilities Perform site qualification, site initiation, interim monitoring, site management activities and close‑out visits (on‑site or remotely) ensuring regulatory, ICH‑GCP, Good Pharmacoepidemiology Practice or protocol compliance and evaluate overall site performance to recommend site‑specific actions. Verify informed consent procedures and protect subject confidentiality, assess safety and integrity issues at sites, and communicate or elevate serious issues to the project team. Conduct source document review, verify CRF data accuracy, resolve queries, and drive query resolution to closure within agreed timelines using electronic data capture tools. Perform investigational product inventory, reconciliation, storage and security reviews and ensure appropriate dispensing and administration according to protocol. Maintain investigator site file accuracy and reconcile with the trial master file, ensuring compliance with local archival regulations. Document activities via letters, reports and logs, support recruitment and retention strategies, and enter data into tracking systems. Manage site‑level activities, budgets and timelines, adapt to changing priorities, and ensure project deliverables are met. Act as primary liaison with study site personnel and collaborate with central monitoring associates to ensure training and compliance. Participate in investigator meetings, sponsor meetings, and global monitoring/project staff meetings, and attend required clinical training sessions. Assist in audit readiness, prepare for audits and manage follow‑up actions. Maintain working knowledge of regulatory guidance, complete required training, and serve as a Site Management Associate II for Real World Late Phase studies. Qualifications Bachelor’s degree, RN or equivalent education, training and experience. Knowledge of Good Clinical Practice, ICH guidelines and applicable regulatory requirements. Proficient computer skills and ability to adopt new technologies. Excellent communication, presentation and interpersonal skills. Capacity for travel up to 75% of the time. Compliance with US residency, privacy, and site access policies. Benefits Company car or car allowance, health benefits (medical, dental, vision), 401(k) match, employee stock purchase plan, commission/bonus eligibility, flexible paid time off and sick time, and other statutory benefits. Salary Range $70,100.00 – $126,100.00. The base salary range represents the anticipated low and high of the Syneos Health range for this position. Equal Employment Opportunity Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender identity, sexual orientation, veteran status, disability or any other legally protected status. #J-18808-Ljbffr Syneos Health, Inc.