Medical Director - Medical Monitoring - Solid Tumor Oncology
Growing CRO seeks an experienced medical monitor to work with their oncology trials
  • Dallas, TX
  • $300,000 - $400,000
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A bit about us:

Our client is a contract research organization, a type of organization that plays a vital role in the development of new treatments and medications for patients. They specialize in a variety of therapeutic areas including Transplants, Oncology, Rare Disease & Cell & Gene Therapy.

Why join us?

In addition to PTO, company-paid holidays, medical, dental and vision insurance our client also boasts the following!
  • Our client has a structured mentoring program to provide the support you need to move forward
  • Our client provides tuition reimbursement and partners with universities and colleges to create programs in our field, and have a dedicated training department
  • Our client has never had a layoff in our 20-year history, support a work-life balance, and have provided cash bonuses every year for the past decade
  • Our client has received multiple awards recognizing it as one of the best places to work in the greater Cincinnati area, as well as one of the top CROs in the industry
  • Our client has consistent double-digit growth rate over the last decade, invest in cutting-edge technology, and pride itself on our average 95% annual retention rate
  • Annual Target bonus
  • 3+ weeks PTO
  • Company credit card for travel expenses

Job Details

Essential Functions:

Act as Medical Monitor for all clinical trials based on the scope of project
Interact with FDA and other regulatory agencies
Review and manage all serious adverse events (SAEs) during course of clinical trials, and participate in managing SAE reporting
Participate in clinical trial study conference calls
Contact investigators and coordinators involved in studies
Provide training for staff and serve as medical resource
Provide medical guidance to regulatory and scientific affairs projects, including but not limited to protocols, IND’s, regulatory documents, clinical study reports, NDA’s and BLAs
Provide medical guidance to real world evidence projects, including but not limited to protocols, patient populations, identifying key thought leaders
Collaborate with multiple team members to ensure medical accuracy in scientific writing projects
Participate in advisory boards and training programs
Serve as mentor to team members and clients
Support Business Development for all departments by providing Medical Expertise and Guidance, attending capabilities meetings, bid defenses, conferences and client meetings as necessary
Identify potential areas of business development and client expansion

Competencies:

Proficient with technology, including Excel, PowerPoint, and Word
Knowledge of GCP and ICH guidelines

Required Education/Experience:

2 years in the pharmaceutical, biotech, or CRO industry
Medical degree, clinical practice, participation / conduct of clinical trials and research
Board certified oncology

Preferred Education/Experience:

5 years in solid tumor - Oncology
Experience leading cross-functional teams
FDA experience
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Job Details
Managed by Jobot Pro
Location
Dallas, TX
Job Type
Permanent
Compensation
$300,000 - $400,000