Happy to announce a new CDM opening with a well-known rising star in the Bay Area biopharma scene. They are a publicy traded, and full funded organization ($400 million in cash and no debt) and for the last 11 years, they've been developing novel pathways for genetic medicine and its applications in a diverse and robust pipeline across three different therapetuics areas. They currently have seven different drug candidates in the clinic which are all being tested with proprietary delivery methods, further advancing both their pipeline and the genetic medicine space overall.
My client is looking to build out their CDM team with a Senior CDM. This role involves leading and performing CDM tasks for all Phase I-IV studies. This role will report to the head of the CDM function directly, and will be part of a highly collaborative and cross-functional team. Requisistes for this role are as follows:
- Based in the Bay Area (must be able to go on-site 4 days a week)
- End-to-End CDM in Clinical Trials Expertise (including Database Lock)
- Experience in DMP and DTP authorship and execution
- Hands-On Experience with Medidata Rave
- Proven Track Record (3 years minimum) of CDM Lead Experience
- CRO Overisght Experience
- 7 years of total Industry Experience in Pharma/Biotech
- Ophthalmology TA Experience is highly preferred
If you or anyone in your network meets the above qualifications, I encourage you to schedule a time for a confidential exploratory call with me using the link below:
https://calendly.com/greg-schoepp/10-minute-job-discussion
