Worldwide Clinical Trials

Medical Director, Medical Affairs - US - Remote

Worldwide Clinical Trials$134K — $267K *
US-AnywhereRemote in Miami, FL
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Medical Degree from an accredited institution
  • 2+ years of medical monitoring experience
  • Strong computer skills (Word, Excel, Access)
  • Fluent in English, both written and spoken
  • Excellent communication, organizational, and time management skills
  • Strong presentation abilities
  • Valid passport for travel as needed

Responsibilities

  • Medically manage assigned clinical trials as Medical Monitor
  • Serve as Global Lead Medical Monitor for designated trials
  • Collaborate on processing Serious Adverse Events with project teams
  • Provide therapeutic and protocol-specific training to teams
  • Contribute to clinical development program designs and protocols
  • Support in writing research papers and client-focused white papers
  • Offer after-hours medical support for assigned projects

Benefits

  • Inclusive and equitable workplace
  • Support for professional development
  • Flexible travel opportunities
  • Engagement in impactful clinical research
  • Access to a competitive benefits package depending on location
Full Job Description
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):

United States of America - $134,500.00 - $267,500.00

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.

About Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Founded
1986

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