Central monitor ii - experience in risk-based monitoring and clinical data management - mexico home based join to apply for the central monitor ii - experience in risk-based monitoring and clinical data management - mexico home based role at syneos health. Syneos health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our clinical development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make syneos health easier to work with, but to make us easier to work for. 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 accelerate the delivery of therapies because we are passionate to change lives. Work here matters everywhere we are passionate about developing our people through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our total self culture – where you can authentically be yourself. Our total self culture unites us globally and we are dedicated to caring for our people. We are continuously building the company we all want to work for and our customers want to work with. When we bring together diversity of thoughts, backgrounds, cultures, and perspectives, we create a place where everyone feels they belong. Job responsibilities bachelor’s degree in a related field, may include life sciences or risk‑based discipline. Minimum of 2 years of clinically related or data‑trend analysis experience; 1 year preferable in clinical research monitoring. Experience working in an rbqm model or similar risk‑based environment preferred. Demonstrated in‑depth knowledge or willingness to learn of appropriate therapeutic indications, regulations, and ich/gcp guidelines as they relate to conducting clinical trials (study management, data management, and regulatory operations). Therapeutic area experience preferred in neuroscience, oncology, immunology, eye care, medical aesthetics, women’s healthcare, or gi. Additional information tasks, duties, and responsibilities as listed in this job description are not exhaustive. The company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education may also be considered, so qualifications of incumbents may differ from those listed in the job description. The company will determine what constitutes equivalent to the qualifications described above. Nothing herein constitutes an employment contract. Language contained herein is intended to fully comply with obligations imposed by the legislation of each country in which it operates, including the implementation of the eu equality directive, in relation to recruitment and employment of its employees. The company commits to compliance with the americans with disabilities act, providing reasonable accommodations when appropriate, to assist employees or applicants in performing essential functions of the job. Seniority level entry level employment type full‑time job function other referrals increase your chances of interviewing at syneos health by 2x mexico city metropolitan area – 2 months ago we’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of ai. J-18808-ljbffr