Clinical Research Methodology Fellow (US/Remote) in Raleigh, NC in Worldwide Clinical Trials

Job title: Clinical Research Methodology Fellow (US/Remote) Company: Worldwide Clinical Trials Job description: 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 3,000 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. What a Clinical Research Methodology Fellow does at Worldwide Clinical Trials This role is therapeutically agnostic and will place a premium upon demonstrating mastery of clinical trial methodology encompassing observational and interventional clinical research. Expertise will be developed through applied clinical research experience, complemented by a didactic program of instruction by various content experts within the Worldwide organization. Assignments can cover any therapeutic area, or any phase of research, and may include drugs, biologics, Advanced Therapy Medicinal Products as well as devices. The position requires training within basic science in an applied scientific discipline as a foundation for competency in clinical research activities. RESPONSIBILITIES: Tasks may include but are not limited to: • Develop articles or other publications in collaboration with other individuals within WCT in order to enhance the image of WCT as a medically minded and scientifically driven organization. • Preparation of articles, white papers, and webinars as well as assistance and protocol and program design. Early Phase: • Development of study concepts for translation into observational or interventional clinical protocols under the direction of the Chief Medical and Scientific Officer, Worldwide. • Independent exploration of the background and implications of evolving science, and clinical trial methodology for specific programs in which participation by Worldwide will be requested. • Development of articles or other publications in collaboration with other scientific, medical, or operational staff within Worldwide to enhance the image of the company as a medically minded and scientifically driven organization, dedicated to the discipline of clinical trial methodology. • Contingent upon a time in the program, representing and/or accompanying the Chief Medical and Scientific Officer of Worldwide for consultation activities with a business development intention. • Support and collaboration with cross-functional and globally diverse staff in resolving client concerns, complaints, or urgent clinical issues referable to protocol design and its impact upon trial operations or analyses OTHER SKILLS AND ABILITIES: • Superb verbal, written and presentation skills are mandatory. • Ability to learn to master the art of clinical trials. • Eagerness to accept instruction and learn. • An established pedigree and training in the scientific method consisting of systematic observation, measurement, experimental design, and the formulation, testing, and modification of hypotheses. REQUIREMENTS: • Ph.D., MD, or PharmD required, with a background of basic research, or clinical research while knowledge of drug discovery/development process was required in the pharmaceutical industry, within contract research organization, or within academia. Candidates from any accredited graduate or professional program will be considered. • Training at a postgraduate level in basic research, clinical research, and scientific study, in either an academic, not-for-profit, or pharmaceutical company setting is required. • Ability to establish a working relationship through teleconference, videoconferences, and as permitted in-person meetings. • Candidate must be available to dedicate two years to the Fellowship program. • Interest and capability in developing expertise in all phases of clinical research is mandatory. Why Worldwide At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient's life depends on it - because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers. Interested in hearing more about Worldwide or our roles? Check out our at www.worldwide.com/careers! #LI-HD1 #LI-Remote Expected salary: Location: Raleigh, NC Apply for the job now! Apply tot his job