Senior Medical Director, Medical Affairs

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 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 Worldwide We 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 us! What the Senior Medical Director, Medical Affairs does at Worldwide Clinical Trials The Senior Medical Director, Medical Affairs will provide medical management and professional medical support for clinical research projects at Worldwide Clinical Trials as the assigned Medical Monitor (MM). This role assists in activities requiring medical and scientific support, including but not limited to assistance with feasibility assessments, medical training, and provision of medical/clinical input to the design of study protocols and/or clinical development programs, as well as assistance with business development activities, as directed by the department head. What you will do Medically manages clinical trials to which they are assigned as MM Serves as Global Lead MM (GLMM) for pan-regional and/or global trials to which they are assigned Collaborates with other members of the Medical & Safety project team to process Serious Adverse Events (SAEs) Provides therapeutic and protocol-specific training to the project teams Contributes medical input into the design of clinical development programs, study protocols, research papers, client-focused white papers, etc. Provides after-hours medical support for projects to which they are assigned Independently 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 management Reviews and/or assists in the preparation of final study reports (CSRs) or other study documentation (protocols, ISS/ISEs, etc.) as directed by senior management Maintains 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 meetings, etc.), reviewing relevant therapeutic/clinical literature, and attending conferences and meetings Interacts with staff in other functional areas within the company to ensure the highest level of client satisfaction through the successful execution of projects Identifies, documents, and appropriately resolves out-of-scope work as directed by senior management Assists in the annual attainment of departmental revenue targets and any other activities as directed by senior management Maintains working knowledge of Good Clinical Practices (GCPs) and regulatory requirements relating to clinical development and safety to assure compliance with ethical, legal, and regulatory standards Mentors 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 company Maintains clinical/therapeutic acumen in medical subspecialty through online and/or in-person scholarly programs/lectures Demonstrates competence with the execution of SAE-related medical review in Worldwide Clinical Trials' electronic safety database Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. What you will bring to the role Excellent computer skills (Word, Excel, Access) Excellent spoken and written English skills Excellent organizational and time management skills Excellent communication skills Excellent presentation skills Your experience Medical degree from an accredited institution of medical education 6-8 years in the Contract Research Organization (CRO), pharmaceutical, or biotechnology industry in a medical monitoring or study physician role Valid passport and ability to travel if required Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit 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. This is who we are. We're a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we're here, you'll get a different answer. And that's what makes us special. Not finding the right fit? Let us know you're interested in a future opportunity by clicking Get Started below or create an account by clicking 'Sign In' at the top of the page to set up email alerts as new job postings become available that meet your interest!