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Full-Time

Head of Clinical Development

Scientific Affairs, Cardiovascular Research

Posted on 6/11/2024

Cleerly

Cleerly

51-200 employees

AI-driven cardiovascular diagnostic solutions

AI & Machine Learning

Compensation Overview

$230k - $300kAnnually

+ Stock Options + 401(k) Match Program

Senior, Expert

Remote in USA

Category
Diagnostics & Laboratory Professionals
Physicians & Surgeons
Medical, Clinical & Veterinary
Required Skills
Communications
Requirements
  • Postgraduate degree MD or PhD in cardiovascular medicine or cardiovascular research.
  • A minimum of 5+ years of clinical trials experience, demonstrating a deep understanding of the clinical research process within Cardiovascular Research.
  • Publication record demonstrating excellent skills in scientific writing and leading publication efforts.
  • Organizational Skills: Exceptional organizational and time management skills to manage multiple projects simultaneously and effectively.
  • Communication Skills: Strong verbal and written communication skills, including effective presentation abilities. Experience serving as primary author and contributor to peer-reviewed journal articles and presentations at scientific meetings.
Responsibilities
  • Sponsor representative towards academic trial leadership, partners and contracts;
  • Oversight of the conduct, progress, relationships, compliance and budgets of clinical trials
  • Overseeing collaborations with cross-functional teams to ensure successful trial execution (Product, Regulatory).
  • Assist in the design of clinical trials, leveraging medical expertise to optimize study protocols and objectives; actively write protocols
  • Maintain a high level of clinical and scientific expertise in the disease area(s) by reviewing the literature, attending medical/scientific meetings, and through personal interchanges with consultants, thought leaders, investigators and internal stakeholders
  • Present at scientific and medical advisory board meetings and at regulatory meetings
  • Contribute to company’s planned regulatory filings including authoring clinical sections for IDEs and other documents for regulatory filings.
  • Regulatory Compliance and Quality: Ensure that all studies conducted adhere to ethical and regulatory standards set forth by the FDA and other relevant governing organizations
  • Cleerly Core Laboratory - Medical Oversight, assist in the design of clinical trials, leveraging medical expertise to optimize study protocols and objectives; actively write protocols
  • Publications and Scientific Writing
  • Contribute to strategic scientific focus and publication plan for Scientific Affairs.
  • Lead scientific review process and scientific writing for multiple publications.
  • Act as a spokesperson for company representing expertise and vision to external stakeholders
  • Stay up-to-date with scientific publications, guidelines, market access and regulatory aspects
  • Drive growth in the clinical trials and research core laboratory business by establishing and nurturing strategic relationships with pharmaceutical, biotechnology, and medical device companies, contract research organizations, and other core imaging laboratories.
  • Develop and maintain relationships with physicians who will review medical images and serve as advisors for the CTSU core lab, fostering a network of trusted experts.

Cleerly offers a digital healthcare platform utilizing AI and coronary computed tomography angiography (CCTA) imaging to precisely identify and define atherosclerosis, enabling personalized treatment plans for heart disease.

Company Stage

Series C

Total Funding

$280.8M

Headquarters

Denver, Colorado

Founded

2017

Growth & Insights
Headcount

6 month growth

5%

1 year growth

15%

2 year growth

87%

Benefits

Medical, dental, and vision plans

Stock Options

401(k) matching program

Company wide holidays

Self-managed PTO

INACTIVE