Fellow, Clinical Research Methodology - US-Remote

Who 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 us!What a Research Fellow Does WorldwideThis position is therapeutically agnostic and will place a premium upon demonstrating mastery of clinical trial methodology through experience, complemented by a program of instruction by various content experts within the WCT organization. Assignments can cover any therapeutic area or any phase of research, and may require an exploration of basic research and clinical research activities for novel technologies for small molecules, biological, or devices.What You Will DoTasks may include, but are not limited to:

• Develop articles or other publications in collaboration with other individuals within WCT 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 with protocol and program design.
• 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.

• Superb verbal, written, and presentation skills are mandatory.
• Ability to learn to master the art of clinical trials.
• Eagerness to accept instruction and learn.

• Ph.D., MD, or PharmD required, with a background of basic research, or clinical research with knowledge of the drug discovery/development process, was required in the pharmaceutical industry, within a contract research organization, or within academia.
• An interest and capability in developing expertise in all phases of clinical research is mandatory.
• The position is remote-based. Travel to Texas once a month is required