Medical Director, Medical Affairs - US - Remote

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 Medical Director, Medical Affairs does at Worldwide

To provide medical management and professional medical support for clinical research projects at WORLDWIDE as the assigned Medical Monitor (MM). To assist in activities requiring Medical 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 s/he is assigned as MM
• Serves as Global Lead MM (GLMM) for pan-regional and/or global trial(s) to which s/he is assigned
• Collaborates with the other members of the Medical & Safety project teams 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 s/he is assigned

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.
• At least 2 years of medical monitoring in clinical research or related industry
• Valid passport and ability to travel as required.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.

The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

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.