Medical Director (Contract)

Medical Director (Contract) Siterois an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation. Job Title: Medical Director Location: United StatesRemote Function: Clinical Services Education: MD or PhD in Gastroenterology & Hepatology or related background Therapeutic Area: Gastro and Hepatology DESCRIPTION: The Medical Director will provide strategic input into current and potential clinical projects, support site investigators and manage the medical monitoring inmanaging all medical aspects of clinical trials. The Medical Director is responsible for strategic input on potential projects that support proposal writing and bid-defense meetings including a deep understanding of therapeutic area’s current clinical research landscape. Support of data review and medical writing for protocols and study specific reports (regulatory annual reports, clinical study report (CSR)). Has experience in FDA interactions examples, all IND support (Pre- submission, Type A, B and C, and IDE support, Pre-Sub, Informal and Submission meetings). The Medical Director will also be responsible for review and addressing site and CRA queries for inclusion/exclusion criteria. The Medical Director will be responsible for preparing listings of protocol deviations and adverse events for regular meetings, performing initial review for coding and reconciling coding based on the inputs of the clinical and medical teams. ESSENTIAL DUTIES ANDRESPONSIBILITIES: Proven track record of Strategy development for FDA submission Protocol development Medical writing support for Protocol, and study reports Experience with FDA interactions Prepare and review protocol deviation listing Codeprotocoldeviationsperprotocoldeviationguidance Prepare drafts of appropriate study plans Prepare adverse event listings Assist the medical monitoring in management ofclinical trials EDUCATION AND EXPERIENCE REQUIRED: Licensed MD or PhD. 2 years of experience workingin clinical trials as a medical monitoring associate or equivalent relevant experience Gastrology; Hepatology Metabolic trial experience (preferred) PREFERREDSKILLS: Strong communication Medical Writing Independent worker Excel CTMS COMPENSATION & BENEFITS: Siteroproudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits. EMPLOYMENT TYPE: Contract; Part time, Hourly COMMITMENTS: Hourly as project requires Willing to work in shifts as and when needed. DISCLAIMER: Siterois an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discriminationon the basis ofrace,color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law. #J-18808-Ljbffr Sitero