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The core competencies we seek are within clinical development, pharmacology, clinical operations, project management, CMC, intellectual property, managing of CROs and vendors, medical writing, and medical sciences.

 

The preferred candidates will possess several of these competencies.

 

Title and salary are commensurate with experience and compliment of competencies, can span from Scientist over Director to VP level, and from $100k to $250k, plus benefits and stock options.

 

CNS Scientist/Pharmacologist

 

Evecxia is hiring a CNS Pharmacologist/Scientist with a strong foundation in neuroscience and pharmacology and a track-record of excellence.

 

Make a positive impact on the lives of millions of people suffering from psychiatric and other CNS disorders. Apply your CNS scientific skills comprehensively across all domains of the drug development process, from animal POC to pivotal clinical trials. Grow, acquire new skills, make your mark, plan your work independently.

 

You will be responsible for scientific input and direct oversight of the preclinical/clinical pharmacology and CMC aspects of the development of Evecxia’s drug candidates. You will have strong analytical capabilities, be a data-oriented independent thinker, be a fast learner, and be capable of wearing many hats. You will be a strong writer, with a wide range of writing/presenting skills, e.g., grants, preclinical protocols, graphing data, regulatory documents, and presentations. Basic statistical data analysis skills are required. You will refer to the Chief Scientific Officer; yet, work across the organization.

 

Click for Background Requirements

  • PhD/PharmD/MD, minimum of 2 years of experience from biotech or pharma, preferably within CNS.
  • Your experience includes several of the following: Defining and carrying out research projects; surveying state of the science; writing preclinical and/or clinical protocols; writing grant applications; writing publications/presentations; perform data analysis: writing regulatory documents; writing clinical documents, etc.
  • Experience with clinical R&D a plus.
  • Experience with drug formulations/CMC a plus.
  • Track record of excellence, e.g., strong first author publication record within CNS, inventor on patents, execution of CNS R&D projects, promotions, recipient of fellowships/grants.

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