Senior Medical Director, Medical Affairs, Neurology
1 week ago
Senior Medical Director, Medical Affairs, Neurology - U.S. - RemoteJoin to apply for the Senior Medical Director, Medical Affairs, Neurology - U.S. - Remote role at Worldwide Clinical TrialsWho We AreWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.Why WorldwideWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join usWhat a Senior Medical Director, Neurology does at Worldwide Clinical TrialsMedical Affairs plays a pivotal role throughout the entire life cycle of a clinical investigation, exerting its influence from the initial stages of Business Development to the final Regulatory Submissions. Within this multifaceted domain, the dedicated members of the Medical Affairs team provide essential support to the broader project team, contributing to the cultivation of the scientific and medical principles that define Worldwide's philosophy.Collaboration is a cornerstone of Medical Affairs, as you work closely with other functional groups within the Worldwide organization.Within Medical Affairs, you will discover a diverse range of roles, including direct interactions with pharmaceutical companies, protocol preparation, feasibility assessments, training of site staff, medical monitoring, pharmacovigilance, and medical writing. These roles present ample opportunities for you to excel and contribute your unique talents to our mission to impact millions of patients' lives around the globeWhat You Will DoCollaborates with other members of the Medical & Safety project teams to process Serious Adverse Events (SAEs)Contributes medical input into the design of clinical development programs, study protocols, research papers, client-focused white papers, etcAs directed supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior managementReviews and/or assists in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc) as directed by senior managementMaintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc), review of relevant therapeutic/clinical literature, and attendance in conferences and meetingsAssists in the mentoring of other medical staff as directed by Senior Management and by consistently displaying exemplary work ethics, compassion, and integrity, supports Senior Management’s leadership of both the department and the companyWhat You Will Bring To The RoleExcellent computer skills (Word, Excel, Access)Excellent spoken and written English skillsExcellent organizational and time management skillsExcellent presentation skillsYour ExperienceMedical Degree from an accredited institution of Medical Education with a Neurology focusAt least 2-4 years of medical monitoring in a CROValid passport and ability to travel as requiredSeniority levelMid-Senior levelEmployment typeFull-timeJob functionHealth Care ProviderIndustriesResearch ServicesTo view our other roles, check out our careers page at www.Worldwide.com or connect with us on LinkedIn.Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. #J-18808-Ljbffr
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Québec City, Canada Worldwide Clinical Trials Full timeA global clinical research organization is seeking a Senior Medical Director for Neurology to lead medical affairs and collaborate with project teams. The ideal candidate will have a Medical Degree with a focus in Neurology and 2-4 years of experience in medical monitoring. Responsibilities include processing Serious Adverse Events, contributing to study...
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Québec City, Canada Worldwide Clinical Trials Full timeMedical Director, Medical Affairs, Psychiatry - U.S. - Remote 4 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it...
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