job summary: This role is for a Pharmaceuticals developing first-in-class therapies designed to reprogram the immune system to achieve antigen-specific tolerance for immune-mediated disease Standard Medical Monitor responsibilities (evaluating AEs/SAEs, responding to safety questions from the site, f/u with PIs, data review). Expectation for this individual is to help with traveling to sites and key conferences across Neuro, GI, Endocrine to meet PIs in person 3 month contract to start (likely will extend beyond that) PR - 125-140/hr, Remote location: Evanston, Illinois job type: Contract salary: $125 - 140 per hour work hours: 9 to 5 education: Doctorate responsibilities: The focus of the Medical Monitor role is to support safety review for all assigned clinical trials, from responding to site questions, providing safety training and guidance to clinical trial sites, to mentoring study teams, reviewing of participant enrollment packets, safety data line listing and participant profile review as applicable, safety information review in documents and processes, safety monitoring at local sites and engaging Key Opinion Leaders and Clinical Investigators. RESPONSIBILITIES: Experience in medical practice and fully trained in all aspects of clinical trials, GCP, and evaluation of adverse events Setting up Data Monitoring Committees (DMCs), participating and presenting Managing their safety vendor, interpreting AEs Site interactions: implementing the protocol, interpreting inclusion/exclusion criteria with sites, facilitating enrollment, working with ClinOps to manage questions/issues from site around logistics Answer specific inclusion/exclusion criteria questionsRespond to safety questions from the sitePerform AE review Review and assess causality on SAEsFollow-up with the Investigator/site for additional information or clarifications as needed Traveling to sites and key conferences across Neuro, GI, Endocrine to meet PIs in person Expected amount of travel (25-30%). qualifications: Qualifications: Must have: MD, 1-5 years' exp, experience working for small biotech. Rare disease or autoimmune experience would be a plus. Will consider candidates with experience in other therapeutic areas. No req. board certifications. #LI-CV1 skills: Clinical research, Medical Information, Medical Plan Development, QC Review Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.