ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.
© All Rights Reserved. ApplyBlast.com
ApplyBlast uses AI to match you with the right jobs, tailor your resume and cover letter, and apply automatically so you can land your dream job faster.
© All Rights Reserved. ApplyBlast.com
Monte Rosa Therapeutics, Inc
This role supports the planning, start-up, maintenance, and closeout of clinical trials within a top-tier Biotech company. The position involves contributing to study-related documents, managing site relationships, and ensuring inspection-readiness of trial documentation. The ideal candidate will be proactive, detail-oriented, and involved in all aspects of clinical trial execution.
Monte Rosa Therapeutics is a biotechnology company pioneering molecular glue degrader (MGD) therapies that promote specific protein ubiquitination and subsequent proteasomal degradation of disease-causing, traditionally undruggable proteins. Their drug discovery platform integrates expertise in MGD chemistry, artificial intelligence, structural biology, and proteomics to rapidly advance programs targeting undruggable or inadequately drugged targets with unprecedented specificity. Focused on cancer and beyond, the company operates out of Boston, MA and Basel, Switzerland.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Monte Rosa Therapeutics, Inc.
Monte Rosa Therapeutics, Inc didn’t post a salary, so this is our estimate from similar listings.
Senior Clinical Trial Associate (CTA)
agomab
Document and Clinical Systems Manager (TMF)
lifelancer
Clinical Trial Associate
Generate:Biomedicines
Clinical Research Regulatory Associate - Contract
Axsendo Clinical Research
Senior Clinical Trial Manager
Summit Therapeutics,
Clinical Trial Coordinator (CTC) — Denmark
MSD