Trebla Talent Jobs in United States

Overview · Position: Senior Medical Director (Clinical Development) · Location: REMOTE · Reports To: Chief Medical Officer · Compensation: base salary + annual bonus + equity · Role Summary · This Senior Medical Director will play a critical role in advancing lead products throug ...

This person will be responsible for the development and execution of global regulatory strategy across the company's clinical portfolio (starting with a late-stage emphasis). This role offers high autonomy, direct ownership of a pivotal submission(s), and the opportunity to lead ...

+This position involves shaping and leading the regulatory strategy across all phases of development. · Global regulatory strategy (Late-Stage Regulatory Interactions – Ph. 3 to commercial) · ...

A leading healthcare recruitment firm is seeking a Vice President of Regulatory Affairs to oversee medical safety across their clinical portfolio. The ideal candidate will have an MD, DO, or MBBS and over 15 years of industry experience, preferably in Neurology or Ophthalmology. ...

Overview · Position: Senior Vice President, Regulatory Affairs · Location: Hybrid (California) · Compensation: $390k-$430k base + annual bonus + equity · Company Description · This is a clinical-stage biopharmaceutical company advancing precision oncology therapies designed to ov ...

A leading healthcare firm is seeking a Senior Medical Director to lead clinical development efforts remotely. The successful candidate will provide strategic medical leadership across Phase I to III studies and support BLA readiness. Applicants must possess an MD and have surgica ...

+Job summary · This Vice President, Drug Safety and Pharmacovigilance, will be the primary physician on the team and responsible for medical safety across its entire clinical portfolio. · +QualificationsMd or Do or Mbbs (Must have clinical training) · 15+ years of industry experi ...

This role will lead the global regulatory function and play a critical role in preparing for an upcoming commercial launch while overseeing regulatory strategy across the entire portfolio. · This group is deeply science-driven and mission-oriented, · a collaborative high-caliber ...

This person will be responsible for the development and execution of global regulatory strategy across the company's clinical portfolio. · ...

Position: Vice President, Regulatory Affairs · Location: Remote/Hybrid · Compensation: k + annual bonus + equity · Role Summary: · This Vice President, Drug Safety and Pharmacovigilance, will be the primary physician on the team and responsible for medical safety across its entir ...

This privately held, Clinical-stage biotech specializes in developing biomarker-driven cancer treatments. · MD or Ph.D with subspecialty training in Oncology · Over 10 years of clinical development industry experience · ...

The Senior Director, Regulatory Affairs, will serve as the Global Regulatory Lead (GRL) and key decision-maker responsible for the development and execution of global regulatory strategy across the company's clinical portfolio.This role offers high autonomy, direct ownership of a ...

The Senior Director, Regulatory Affairs, will serve as the Global Regulatory Lead (GRL) and key decision-maker responsible for the development and execution of global regulatory strategy across the company's clinical portfolio. · Global regulatory strategy (Late-Stage preferred) ...

A leading clinical-stage biopharmaceutical company is seeking a Senior Vice President of Regulatory Affairs to lead the global regulatory function. The role requires an advanced degree and experience in late-stage development. You will oversee regulatory strategies for a commerci ...

This Senior Medical Director will play a critical role in advancing lead products through late-stage clinical development, · providing medical leadership across Phase I–III studies, · and supporting BLA readiness. · ...