Remote Site Monitor I/II PPD is a leading global contract research

organization. At PPD we are passionate, deliberate, and drive by our purpose to improve health. Remote Site Monitoring and Management (RSMM) blends on and off-site monitoring functions, providing efficiency to our clients. The RSMM group provides global time zone coverage and optimizes technology. Working in the RSMM group, you will contribute directly to PPD's strategy to bend the time and cost curve of drug development by providing adaptive and intelligent monitoring services to our clients. As a Remote Site Monitor (RSM), you will use a variety of tools and technologies to review study data. You will interact with study sites via phone, supporting the site teams and monitoring subject enrollment for the study. As a RSM you embody ethical research and business conduct, ensuring we never compromise quality or patient safety. Grow within the RSM career path as a Senior or Principal RSM, develop into a Clinical Research Associate, or move into other roles or departments within Global Clinical development. At PPD we hire the best, develop ourselves and each other, and recognize the power of being one team. It's not just talk - our award winning training programs speak for themselves. Join PPD in our relentless pursuit of excellence - apply now! Education and Experience: * Bachelors Degree in a life science-related field or relevant/equivalent combination of education, training and experience that provides the individual with the required knowledge, skills, and abilities. * Prior clinical research experience 0-1 year as well as knowledge of clinical monitoring through classwork/training that provides the required knowledge skills and abilities. In some cases, previous experience in a clinical environment where experience is gained in clinical trials, data management, medical terminology, medical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered. * Prefer individuals who aspire to advance into a CRA role. Knowledge, Skills and Abilities: * Basic medical/therapeutic area knowledge and understanding of medical terminology * Ability to attain and maintain a working knowledge of FDA and/or local regulation and guidelines, ICH GCPs and PPD procedural documents * Ability to successfully complete PPDs Clinical Foundation Training Program (CFP) * Ability to evaluate medical research data * Ability to advise, counsel, and motivate investigational sites * Effective oral and written communication skills with the ability to communicate effectively with medical personnel * Excellent interpersonal and customer service skills

• Good organizational and time management skills * Proven flexibility and adaptability * Strong attention to detail * Ability to work in a team or independently, as required· * Good computer skills with good knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn appropriate software * Ability to extract pertinent information from all study documents, such as protocols, electronic study data systems, CTMS and dashboard * Excellent English language and grammar skills Physical Requirements: * Ability to work in an upright and/or stationary position for 6-8 hours per day. * Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. * Frequent mobility required. * Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. * Occasional light lifting and/or carrying of objects with a maximum lift of 5-15lbs.(2-6kgs.) * Ability to access and use a variety of computer software developed both in-house and off-the-shelf. * Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. * Frequently interacts with others to obtain or relate information to diverse groups. * Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task. * Regular and consistent attendance. Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and/or local law. **Primary Location: **North America-United States-North Carolina-Wilmington **Work Locations: ** **Job: **Clinical Management **Organization: **Pharmaceutical Product Development, LLC.