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Full Time Nimble Therapeutics Jobs (NOW HIRING)

Vistera Inc

Senior Scientist, Research

Waltham, MA · On-site

$107K - $136K/yr

... therapeutics. This individual will play a key role in drug discovery programs by conceiving ... This is a full-time, on-site position located at Visterra's headquarters in Waltham, MA.

Arrowhead Pharmaceuticals

Senior Buyer

San Diego, CA

$70K - $85K/yr

Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is ... Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to ...

Arrowhead Pharmaceuticals

Senior Buyer

Madison, WI

$70K - $85K/yr

Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is ... Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to ...

Arrowhead Pharmaceuticals

Senior Buyer

San Diego, CA · On-site

$70K - $85K/yr

Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is ... Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to ...

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Full Time Nimble Therapeutics information

What is the difference between Full Time Nimble Therapeutics vs Full Time Biotech Research Associate?

AspectFull Time Nimble TherapeuticsFull Time Biotech Research Associate
Required CredentialsBachelor's or Master's in Life Sciences, relevant lab experienceBachelor's or Master's in Life Sciences, laboratory skills
Work EnvironmentResearch labs focused on drug discovery and developmentLaboratories conducting biomedical research and experiments
Employer & Industry UsageBiotech and pharmaceutical companies, research institutionsBiotech firms, pharmaceutical companies, research organizations

Full Time Nimble Therapeutics and Full Time Biotech Research Associate roles both require similar educational backgrounds and lab experience. Nimble Therapeutics focuses on drug discovery projects, while Biotech Research Associates may work across various research areas. Both positions are integral to biotech industries, but Nimble Therapeutics emphasizes therapeutic development specifically.

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Infographic showing various Full Time Nimble Therapeutics job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 5% Part Time, and 1% Contract. Highlights an 86% Physical, 6% Hybrid, and 8% Remote job distribution.

Senior Medical Director, Oncology

Redwood City, CA • On-site

Corcept Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Corcept Therapeuticsexternal

$298K - $350K/yr

Full-time

Re-posted 26 days ago

Job description

Responsibilities:

  • Design and implement Phase I to III clinical studies
  • Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents
  • Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs
  • Act as a clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs
  • Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports
  • Act to provide medical oversight and safety monitoring for ongoing clinical trials including participation in SAE reporting and serving on the safety committee
  • Play a key role in the analysis, interpretation and delivery of high-quality clinical data
  • Interact with principal investigators and opinion leaders to facilitate clinical trials research
  • Participate in appropriate regulatory discussion and activities, including the filing of IND's, CTXs, NDA/MAAs, throughout the development cycle
  • Provide training and ongoing input to all members of the clinical team on medical and scientific issues related to the therapeutic field in question
  • Participate in clinical study report conceptualization, development and writing for global regulatory submissions
  • Work closely and collaboratively with other functions, e.g. clinical operations, safety, biometrics, regulatory, medical writing, medical affairs and commercial
  • Develop and give internal and external presentations as subject matter expert for the therapeutic area
  • Participate in the development and review of publications
  • Participate in the management of human resources in a matrixed environment - recruitment, performance management, succession planning, talent management, etc.

Preferred Skills, Qualifications and Technical Proficiencies:

  • Demonstrate strong clinical and scientific knowledge
  • Is an excellent communicator with proven leadership skills and the ability to interact in a cross functional environment
  • Feel comfortable in a fast-paced and nimble small company environment and able to adjust workload based upon changing priorities

Preferred Education and Experience:

  • MD, board-certified (or eligible)
  • Expertise in Oncology
  • A strong track record of scientific activity, demonstrated by publications in top tier journals
  • At least 6+ years of relevant clinical development experience
  • Relevant basic and/or clinical research experience in academic settings is viewed favorably

The pay range that the Company reasonably expects to pay for this headquarters-based position is $298,000-$350,600; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

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