Remote OK
$130k–$175k/yr
Job Description: Senior Software Engineer The Senior Software Engineer is responsible for architecting, designing, and delivering enterprise-grade clinical data intelligence platforms within a global clinical research or…
Skills: Software Architecture, AI-Native Development, Python, React, TypeScript
Quebec, Quebec, Canada · Remote OK
Job Description: Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary…
Skills: Medical Writing, Regulatory Documentation, ICH Guidelines, Scientific Analysis, Statistical Interpretation
Massachusetts, United States · Remote OK
$67k–$80k/yr
Job Description: Proposals & Contracts Specialist Under the direction of management or an experienced Proposals lead, the Proposals & Contracts (“P&C”) Specialist is responsible for the development of proposals and contr…
Skills: Proposal Development, Contract Management, Clinical Research, Salesforce, Microsoft Word
Massachusetts, United States · Remote OK
$132k–$151k/yr
Job Description: Key Purpose: The Principal Medical Writer independently plans and prepares a range of regulatory documents and/or medical communications to support all phases of product development. The primary responsi…
Skills: Medical Writing, Regulatory Writing, Manuscript Preparation, ICH Guidelines, ICMJE Guidelines
Massachusetts, United States · Remote OK
$132k–$151k/yr
Job Description: Key Purpose: The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibil…
Skills: Regulatory Writing, Nonclinical CTD, ICH Guidelines, Medical Communications, Project Leadership
California, United States · Remote OK
$160k–$200k/yr
Job Description: Senior Business Development Director – Regulatory & Medical Writing The Senior Business Development Director - Regulatory & Medical Writing is responsible for driving growth of Veristat’s Regulatory Scie…
Skills: Business Development, Regulatory Affairs, Medical Writing, Consultative Selling, Contract Negotiation
California, United States · Remote OK
$185k–$200k/yr
Job Description: Senior Business Development Director The Senior Business Development Director is responsible for the development and expansion of new business opportunities within established accounts and prospective cl…
Skills: Business Development, Sales Lead Generation, Contract Negotiation, Client Presentations, Proposal Development
Massachusetts, United States · Remote OK
$116k–$128k/yr
Job Description: Position specific overview The Senior Medical Writer- Clinical Focus is a major contributor to document authorship for a variety of documents across different service lines. The Sr Medical Writer will be…
Skills: Regulatory Writing, Clinical Study Reports, Investigator Brochures, Protocol Development, Microsoft Word
Riga, Latvia · Remote OK
Job Description: Key Purpose: The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibil…
Skills: Medical Writing, Regulatory Writing, ICH Guidelines, Clinical Study Reports, Protocols
North Carolina, United States · Remote OK
$130k–$190k/yr
Job Description: Senior Business Development Director – Regulatory & Medical Writing The Senior Business Development Director - Regulatory & Medical Writing is responsible for driving growth of Veristat’s Regulatory Scie…
Skills: Business Development, Regulatory Affairs, Medical Writing, Consultative Selling, Contract Negotiation
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Architect and deliver enterprise-grade clinical data intelligence platforms using AI-native development methodologies. Enhance software velocity and quality through AI-orchestrated workflows to support life-changing therapies.
Requires a Bachelor's degree and at least 4 years of software engineering experience with a focus on production-grade systems. Proficiency in Python, React/TypeScript, and experience with AI coding assistants and DevOps practices is essential.
The Senior Software Engineer is responsible for architecting, designing, and delivering enterprise-grade clinical data intelligence platforms within a global clinical research organization. This role operates within a high-impact team that leverages AI-native development methodologies to accelerate the design and deployment of scalable software solutions.
The position will enhance software development velocity and quality through AI-orchestrated workflows, contributing directly to the advancement of clinical research technologies that support the development of life-changing therapies, including oncology and rare disease treatments.
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
What we offer:
The estimated hiring range for this role is $130K – 175K plus applicable bonus. This hiring range is specific to the USA and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
What we look for
Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
#LI-SI1
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile. Veristat. - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at [email protected]. Be vigilant.
Offices: 134 Turnpike Rd, Ste 200, Southborough, Massachusetts 01772, US · 2801 Slater Road, Ste 100, Morrisville, North Carolina 27560, US · TAIPEI, Hsin Ji 9F-1., No.460, Sec. 4 Xinyi Rd., Xinyi Dist., Taipei City, 11052, TW · 36 rue de l'intendance, Lotissement de l'intendance, Fréjus, 83600, FR · Carrer de Sant Antoni, Maria Claret 167, Barcelona, 08025, ES
Veristat is the science-first full-service drug and biologic CRO and consultancy that integrates strategic planning, regulatory expertise, and clinical trial execution to rapidly advance the most complex or novel therapies. At Veristat, we collaborate with clients to support the rapid delivery of life-changing therapies, helping them make sound decisions amidst uncertainties. Our scientific experts design and conduct the global activities required for any clinical, regulatory, or commercialization program comprehensively and efficiently. With our focus on novel drug development and nearly 30 years of experience, our versatile approach and bold scientific thinking make the impossible possible. Depend on our game-changing expertise and reliable execution for fast results and positive impact to support your biologics and drugs to treat rare cancers, CNS/Neurological disorders, Endocrine/metabolic disorders, and infectious diseases. We are…Bold. Scientific. Versatile. Veristat. - Veristat has recently been made aware that unknown third parties that have no connection to Veristat are generating fake Veristat job postings, interviews, and even fake employment offers via emails, websites, and various social media platforms, seemingly for the purpose of fraudulently obtaining personal information from legitimate job candidates. All legitimate correspondence from Veristat will originate from our applicant tracking system (Jobvite) or an @veristat.com email address. If you have received outreach from someone claiming to be a member of our team please search our official LinkedIn company page (https://www.linkedin.com/company/veristat-llc), where all members of our authorized recruiting team can be identified, or contact us directly at [email protected]. Be vigilant.
Offices: 134 Turnpike Rd, Ste 200, Southborough, Massachusetts 01772, US · 2801 Slater Road, Ste 100, Morrisville, North Carolina 27560, US · TAIPEI, Hsin Ji 9F-1., No.460, Sec. 4 Xinyi Rd., Xinyi Dist., Taipei City, 11052, TW · 36 rue de l'intendance, Lotissement de l'intendance, Fréjus, 83600, FR · Carrer de Sant Antoni, Maria Claret 167, Barcelona, 08025, ES
