Guide and partner with science volunteers to create scientific statements, clinical practice guidelines, and educational programs.
Serve as in-house science expert, consulting on programs, press releases, and professional content across the Association.
Synthesize and explain current cardiovascular science and medicine to staff, volunteers, and the public.
The American Heart Association is a nonprofit organization dedicated to reducing cardiovascular disease and stroke, advancing science and public health. Since 1924, it has built a large national community with a collaborative culture, offering professional development and work-life harmonization for employees.
Support clinical development strategies and study execution across Phase 1-3 programs.
Oversee clinical safety and data review, partnering with CROs and internal teams to ensure quality.
Contribute to protocols, regulatory documents, and study reports for respiratory disease therapies.
Celea Therapeutics is a biopharmaceutical company dedicated to advancing transformative treatments for serious respiratory diseases, with its lead program in Phase 3 clinical development. As an early-stage, mission-driven team, Celea values accountability, transparency, collaboration, innovation, and passion.
Serve as study statistician for Phase 1-3 vaccine clinical trials, leading statistical design, analysis, and reporting.
Oversee statistical CROs, develop analysis plans, and ensure regulatory and scientific rigor.
Provide statistical consultation across CVIA programs and represent PATH at scientific meetings.
PATH is a global nonprofit dedicated to achieving health equity, developing and scaling innovative solutions to pressing health challenges. With more than 40 years of experience, PATH fosters a culture of collaboration and partnership across diverse teams.
Lead and grow a multidisciplinary team focused on applied scientific research, biomedical data stewardship, and community engagement around Sage’s data assets.
Oversee data management, curation, and governance to ensure FAIR and GA4GH-aligned sharing, and champion data quality and harmonization for cross-study reuse.
Represent Sage externally with data generators, researchers, and funders, while mentoring team members and contributing to grant proposals and funding strategies.
Sage Bionetworks uses open science and collaboration to improve human health, bringing together scientific, technical, and operational expertise to advance biomedical research. A Seattle-founded nonprofit since 2009, they value curiosity, diverse perspectives, and radical collaboration with a mission-driven, interdisciplinary team.
Provide statistical leadership across clinical development programs from early-phase through late-phase trials.
Lead clinical trial design, develop SAPs, and oversee statistical analyses for regulatory submissions.
Collaborate with cross-functional teams and mentor statisticians to ensure scientific rigor and regulatory compliance.
ClinChoice is a global full-service CRO providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, it fosters a quality-driven 'one-team' culture focused on continuous training and diversity.
Provide medical direction and oversight for clinical trials, including safety monitoring and medical data review.
Partner with GCO to build client relationships and support proposals, feasibility, and business development.
Serve as drug development SME, contributing to protocols, training, and medical strategy across studies.
Fortrea is a global contract research organization providing clinical development and trial management services to pharma/biotech. It fosters a collaborative, family-like culture focused on advancing life-saving therapies.
Support the development and execution of clinical regulatory strategies for assigned programs across regions.
Prepare and manage IND applications and other regulatory submissions, ensuring accuracy and timely delivery.
Provide regulatory guidance to cross-functional teams and participate in health authority interactions.
Zai Lab is an innovative, research-based biopharmaceutical company based in China and the US, focused on bringing transformative medicines for oncology, autoimmune disorders, infectious diseases, and neurological disorders to patients worldwide. Founded in 2014, Zai Lab has a global team of approximately 2000 employees and is committed to gender diversity and environmental responsibility.
Drive revenue growth and strategic partnerships for biometrics services across biotech and pharma.
Lead complex deal pursuits, manage pipeline in Salesforce, and exceed revenue targets.
Serve as a trusted advisor to senior client stakeholders and shape go-to-market strategy.
eClinical Solutions helps life sciences organizations accelerate clinical development through expert data services and the elluminate Clinical Data Cloud. It is a fast-growing, people-first company recognized for remote work culture and diversity, offering a collaborative environment.
Lead integrated publication strategies and scientific communications for Kardigan's cardiovascular portfolio.
Oversee publication governance, compliance, and medical information operations.
Collaborate cross-functionally to translate scientific evidence into congress presentations and resources.
Kardigan is a heart health company developing targeted treatments to make cardiovascular disease preventable and curable. It has an industry-leading team and a culture driven by patients, authenticity, and curiosity.
Lead analytical strategy and method lifecycle management for small molecule drug substance and drug product development.
Oversee external analytical partners, CDMOs, and testing laboratories to ensure cGMP compliance and quality.
Support regulatory submissions, specifications, stability programs, and commercialization readiness.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease and obstructive sleep apnea. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote company.
Lead the development of annual and multi-year congress strategies across Kardigan's cardiovascular portfolio.
Oversee full congress lifecycle execution, including planning, medical booth, KOL engagement, and post-congress insights.
Build insight-generation frameworks and partner with scientific communications to extend congress impact through omnichannel channels.
Kardigan is a heart health company working to make cardiovascular disease preventable, curable and no longer the leading cause of death in the world. Led by the co-founders of MyoKardia, we have a cutting-edge discovery platform, a late-stage pipeline, and an industry-leading team driven to improve patients' lives.
Build and strengthen strategic partnerships with clinical research sites and site organizations across an assigned region and therapeutic area.
Act as an enterprise-level partner engaging senior executives and C-suite stakeholders to establish durable, mutually beneficial relationships.
Drive improved clinical trial execution through collaboration, reduced startup timelines, and measurable quality standards.
The company is a healthcare organization focused on improving clinical trial execution through strategic partnerships with research sites. It fosters a collaborative and inclusive environment supporting leadership development and meaningful impact on patient outcomes.