Tag: Regulatory

Senior Product Designer

Marky Mark

Pear Therapeutics is the leader in prescription digital therapeutics or PDTs. Pear aims to redefine medicine by discovering, developing, and delivering clinically validated software-based therapeutics to provide better outcomes for patients, smarter engagement and tracking tools for clinicians, and cost-effective solutions for payers. Pear has a pipeline of products and product candidates across therapeutic areas, including the first three PDTs with disease treatment claims from the FDA. Pear’s lead product, reSET®, Read More …

Mobile Engineer (React/ReactNative) – Remote

Marky Mark

Come use your engineering talents to help people living with serious diseases. We’re starting with addiction, insomnia, multiple sclerosis (MS), and schizophrenia, and there’s more to come. Pear’s deep knowledge and experience in the biotech space has set us up with phenomenal partnerships and a strong product roadmap. Our engineers are platform-izing our architecture and building new mobile applications.   TEAM: Our team of engineers, based in San Francisco and Boston, Read More …

Design Assurance Engineer – Remote

Marky Mark

About Pear Therapeutics: Pear Therapeutics is the leader in prescription digital therapeutics. We aim to redefine medicine by discovering, developing, and delivering clinically validated software-based therapeutics to provide better outcomes for patients, smarter engagement and tracking tools for clinicians, and cost-effective solutions for payers. Pear has a pipeline of products and product candidates across therapeutic areas, including severe psychiatric and neurological conditions. Our first product, reSET®, treats Substance Use Disorder and Read More …

Senior Clinical Scientist

Marky Mark

The Senior Clinical Scientist will assist the Chief Medical Officer (and/or designated Development Lead) in all areas of clinical development strategy, study protocol development, ongoing clinical data review, evaluation, documentation and reporting. You will be responsible for all scientific aspects of a study or studies and have a leading role providing clinical science input into regulatory strategy and documents.   KEY RESPONSIBILITIES Assist in scientifically sound development of the clinical portions Read More …