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Medical Director

Company: TriWorth
Location: Deerfield
Posted on: September 14, 2022

Job Description:

**This is a work from home position that can be worked remotely from anywhere in the United States***The Medical Director is responsible for delivery of medical monitoring services, including, but not limited to, working with clinical project teams to monitor the safety of ongoing studies, and support database locks. The MD will work with the clinical teams to review the safety data including review of MedWatch/CIOMS forms. This individual must have the ability to work and communicate efficiently with internal and external partners. The MD must be a licensed Medical Doctor (MD) or Doctor of Osteopathy (DO) preferably with experience in Oncology. A minimum of five (5) years of industry experience and in depth knowledge of, and experience as, a medical monitor for clinical trials (Phase I - III) is necessary. This individual must possess strong verbal and written communication competencies as well as interpersonal skills with experience participating on project teams, coordinating safety activities and adhering to tight timelines. The MD will attend regularly scheduled meetings as required and respond to site, sponsor and Health Authority questions. He/she will attend and present at Investigator meetings, review CRFs, present study updates as needed, train in-house staff and project teams, design and implement safety monitoring plans, conduct data base listings (DBL) final reviews, review blinded tables, listing & figures (TLFs), review protocol deviations, and participate in all DBL meetings as assigned. The MM will review final TLFs, work with the medical writer(s) to review & revise Clinical Study Report (CSR) documents, review discussion and conclusions, and participate in comment resolution meetings. The MD may present topline results to Sponsors or Competent Authorities. Other tasks may be required as determined by the project. The position is preferably based in the Chicago, IL, area but working remotely with occasional face to face meetings is acceptable depending on business needs. He/she will need to be present in the Deerfield, IL, office for initial onboarding/training.Advanced Clinical is a global clinical development organization that provides CRO, FSP, Quality & Validation, and Strategic Resourcing services for biopharmaceutical and medical device organizations. Our mission is to deliver a better clinical experience for our clients. With global experience in over 50 countries, we are committed to improving all lives touched by clinical research. We understand the complex nature of the clinical research industry and approach each opportunity with compassion. Together, we answer the hopes of patients and healthcare professionals with industry-leading services in global life-sciences. As part of the Advanced Group family of companies, Advanced Clinical employees provide the support, structure, and professional background and experience for better clinical trials and research. They are the foundation of our energetic and collaborative environment, where constant learning and service to others take top priority. We seek dynamic, hard-working team members who are inspired to work amongst diverse backgrounds and perspectives. From our altruistic mission to outstanding career development opportunities, there's no better place to grow your career than Advanced Clinical.Assist with RFP/RFI completion and attend sales meetings as requested by Business DevelopmentOversees the management of medical monitoring during the course of clinical trials and projectsOversees medical review of key clinical documents, individual case safety reports, and medical or safety-related regulatory documentsProvides support and input into the planning, design, preparation, initiation, and execution of study protocols and other required documentation in compliance with project plans, federal regulations, GCP, and good medical practice. May participate in the evaluation and selection of investigators and study sites as well as analysis of medical activitiesEnsures delivery of medical/clinical direction to investigative sites per contract deliverablesPrepares medical and safety plans for clinical trials/servicesOversees collection, review, guidance and manages overall safety case processing as dictated by client contracts Oversees reviews and directs medical and safety sections of regulatory document submissionsMay participate in Investigator meetingsDevelops and assists other staff in the development of processes, timelines, planning, and strategyFacilitates collaboration and communication with medical/scientific personnel and ensures that the most current research information is accessible for reviewThis individual requires an excellent understanding of the clinical/pharmaceutical process so as to effectively communicate and create required deliverables. Possesses advanced knowledge of, and ability to, apply ICH GCP and all applicable FDA and international pharmacovigilance regulations and guidelines. Possesses exceptional leadership skills and proven industry vision. Requires effective negotiation and interpersonal communication skills to interact with a variety of peers and constituents. Must have the ability to understand complex clinical and statistical data and issues from an analytic standpoint. Education: Medical Doctor (MD) or Doctor of Osteopathy (DO) from an accredited university. Specialty in oncology preferred. Certification: Preferably board certified in the US.Experience: Minimum of five (5) years of clinical research and medical/safety management experience in the pharmaceutical industryAt Advanced Group, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. A diverse staff allows us to effectively draw on different perspectives and enhance our efficiency and effectiveness. Diversity thereby strengthens the legitimacy and relevance of Advanced Group in delivering services to our clients.We seek talented, creative individuals from a variety of backgrounds and cultures to work with us. It is our priority that our workplace be inclusive, welcoming of diverse ideas and appreciative of valuable experience.Equal Employment OpportunityIt is Advanced Group's practice not to discriminate against any Employee or applicant because of sex, race, color, age, national origin, religion, gender, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, physical or mental disability, medical condition, military or veteran status, or any other basis protected by applicable federal, state, or local law.This practice applies to all terms and conditions of employment including, but not limited to, hiring, training, compensation, benefits, promotions, transfers, layoff, Company-sponsored education, social and recreational programs, and treatment on the job. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your Recruiter so that we can meet to discuss the appropriate alternatives available.#LI-MF2

Keywords: TriWorth, Arlington Heights , Medical Director, Executive , Deerfield, Illinois

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