$69K - $115K *
Lead the charge in delivering exceptional medical writing services for clinical documentation, ensuring compliance with regulatory standards while managing project timelines and collaboration with cro...
Today
$69K - $115K *
Empower regulatory writing and publication efforts by collaborating with scientists and stakeholders. Lead documentation projects, ensuring adherence to industry standards while managing timelines and...
Today
Principal Medical Writer - Publications
$110K - $130K *
Collaborate with cross-functional teams to produce high-quality medical documents, guiding projects with regulatory expertise. Lead writing, peer review, and client interactions, ensuring compliance a...
4 days ago
Principal Medical Writer - Publications
$110K - $130K *
Execute high-quality medical writing for complex deliverables, ensuring compliance with regulatory standards. Collaborate with cross-functional teams, mentor junior writers, and maintain strategic ali...
5 days ago
Principal Medical Writer (Regulatory)
$110K - $130K *
Transform the regulatory landscape as a principal medical writer, managing complex deliverables and ensuring clarity in scientific communication while collaborating across departments and mentoring pe...
2 weeks ago
Senior/Principal Medical Editor - FSP
$110K - $130K *
Elevate medical editing standards by leading complex projects, training teams, and ensuring compliance with regulatory guidelines while delivering high-quality medical documents on time and on budget...
2 weeks ago
Senior/Principal Medical Editor - FSP
$110K - $130K *
Shape the future of medical writing by leading complex projects and mentoring teams. Ensure compliance with industry standards while delivering high-quality editorial support across various documentat...
2 weeks ago
$130K - $146K *
Shape user experiences by creating intuitive UX content, collaborating with cross-functional teams to simplify healthcare data products, ensuring clarity and user-centric designs...
Reposted 4 weeks ago
Medical Director (Publications)
$130K - $150K *
Champion effective publication strategies and lead scientific communication initiatives, acting as a strategic partner to clients and teams. Navigate complex medical affairs content to drive impactful...
1 week ago
Regulatory Affairs Consultant - Submissions Manager
$110K - $130K *
Shape the future of regulatory submissions through strategic management, collaboration, and expert oversight. Lead cross-functional teams in delivering compliant submissions to global health authoriti...
4 days ago
Senior Direct Response Copywriter
$90K - $110K *
Create compelling, conversion-driven copy in a high-growth environment. Collaborate across teams to manage direct response marketing initiatives, optimize messaging for diverse channels, and translate...
2 weeks ago
$89K - $148K *
Unlock potential by leading the development of advanced clinical data analytics solutions, enhancing reporting capabilities, and driving operational excellence to support Data Sciences and stakeholder...
Reposted 3 days ago
$89K - $148K *
Explore a dynamic role in Clinical Data Analytics, enhancing reporting, analysis, and performance metrics to support clinical studies. Collaborate with cross-functional teams to deliver innovative sol...
3 days ago
Senior Regulatory Affairs Consultant - (Post Approval CMC Authoring - Vaccines or Biologics)
$120K - $145K *
Partner with us to drive global CMC regulatory strategies for biologics and vaccines. Take ownership of submissions and lifecycle management. Collaborate closely across functions to ensure compliance...
6 days ago
Regulatory Strategy Senior Associate
$100K - $120K *
Shape the future of regulatory strategy by supporting initiatives for new treatments. Collaborate cross-functionally, navigate compliance, and influence outcomes in a fast-paced, growth-oriented envir...
2 weeks ago
Medical Monitor (Canada Board-Certified Gastroenterologist)
$210K - $250K *
Join a team that provides critical medical insights for clinical studies, ensuring patient safety and regulatory compliance while enhancing trial quality through expert medical monitoring and collabor...
1 week ago
Associate Director, Regulatory Affairs & Submissions - Nonclinical Development
$125K - $150K *
Serve as a strategic regulatory leader, guiding nonclinical drug development and ensuring compliance for successful clinical entry and regulatory submissions, collaborating with cross-functional teams...
3 weeks ago
$110K - $130K *
Lead our team in coding and programming advanced R and SQL data solutions, utilizing real-world data sources to deliver impactful analytics and insights while ensuring project timelines and team colla...
Reposted 3 weeks ago
Sr Dir/Director, Strategy & Planning - Real World Late Phase/Real World Evidence
$150K - $180K *
Join a dynamic team to provide strategic oversight and commercial leadership for Real-World Late Phase portfolios. Drive sponsor growth through effective planning, proposal development, and integrated...
2 days ago
Sr Dir/Director, Strategy & Planning - Real World Late Phase/Real World Evidence
$150K - $180K *
Drive strategic leadership and oversight for real-world late-phase projects, guiding teams from proposal development to study execution while fostering client relationships and ensuring alignment on o...
3 days ago
Project Manager, Market Access & HEOR
$100K - $120K *
Join a dynamic team to lead market access projects, manage client needs, and deliver strategic HEOR solutions. Utilize your expertise in Canadian and US healthcare to enhance evidence generation and d...
1 week ago
Senior Group Underwriting Best Practice Analyst
$73K - $101K *
Partner with us to enhance Group Underwriting processes, lead initiatives, and implement training. Drive efficiency and continuous improvement while collaborating with diverse teams in a dynamic and s...
4 weeks ago
$90K - $105K *
Lead the integrated media buying and execution efforts, enhancing campaign performance through strategic relationships with key publishers and thorough training of team members. Drive innovative solut...
Reposted 3 weeks ago
Senior Technical Content Writer
$100K - $120K *
Champion the creation of technical content for data platforms, targeting data engineers and analytics experts. Generate valuable ebooks, guides, and blog posts that drive comprehension and engagement...
1 week ago
Senior Regulatory Affairs Consultant - Senior Regulatory Project Manager
$125K - $150K *
Lead the charge in shaping global regulatory strategy to deliver transformative vaccines. Collaborate with cross-functional teams and senior leadership to ensure timely regulatory milestones while fos...
6 days ago