Oversee critical monitoring activities across clinical trials, ensuring compliance with protocols and regulations.
Collaborate with investigators and site teams to maintain study integrity and operational excellence.
Support Phase II and Phase III trials in challenging therapeutic areas to improve patient outcomes.
Jobgether uses artificial intelligence to match job seekers with opportunities through a fair and efficient process. As a growing platform, they emphasize collaboration, integrity, and patient impact in their culture.
Lead integrated evidence-generation and publication strategies across the company's portfolio.
Identify evidence gaps and develop research plans to disseminate clinical, real-world, and economic data.
Partner with cross-functional teams including Medical Affairs, Clinical Development, and Regulatory to align on scientific priorities.
Freenome is a biotechnology company developing cancer screening tests using multiomics and liquid biopsy. As a growing organization, they emphasize diversity, equity, and inclusion in a collaborative culture.
Lead clinical trial strategies and evidence-generation initiatives for diagnostic product development and regulatory submissions.
Serve as a scientific expert guiding study design, interpreting clinical data, and collaborating with stakeholders.
Ensure successful clinical programs across US and EU markets, ensuring scientific rigor and regulatory alignment.
The company develops innovative diagnostic solutions. They foster a collaborative environment emphasizing scientific excellence, continuous learning, and impactful solutions.
Monitor and own the progress of clinical studies at investigative sites.
Ensure studies are conducted per protocol, SOPs, ICH-GCP, and all applicable regulations.
Coordinate setup activities including investigator identification and regulatory submissions.
Precision for Medicine is a CRO integrating clinical trial execution with scientific and lab expertise, focusing on Oncology and Rare Disease. They have a strong culture with high CRA retention and emphasize work-life balance.
Lead and manage a team of MSLs across the West region, coordinating medical and scientific liaison activities with internal and external stakeholders.
Develop and execute comprehensive territory medical plans, foster relationships with key opinion leaders, and ensure high-quality scientific exchange.
Recruit, train, and develop high-performing MSLs, and contribute to product development strategy and launch planning.
BridgeBio is a biopharmaceutical company that uses a pooled project model to reduce risk and accelerate development of life-changing medicines for rare diseases. They foster a culture of curiosity and experimentation with small teams of experts and a focus on innovation.
Lead a 6-person MSL team in Plastics & Regenerative Medicine while maintaining a personal field territory.
Ensure scientific engagement plans align with brand strategy and medical objectives.
Provide coaching, training, and performance management to the MSL team.
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. The company operates globally in immunology, oncology, neuroscience, and aesthetics.
Provide statistical leadership across clinical research projects, ensuring high-quality methodologies and analyses.
Collaborate with cross-functional teams to support innovative study designs and advanced statistical modeling.
Author and review Statistical Analysis Plans (SAPs), tables, listings, and figures for regulatory submissions.
The partner company provides advanced statistical expertise and scientific leadership within a collaborative biometrics and data science environment, supporting complex clinical research projects across multiple therapeutic areas. The company fosters a collaborative and supportive culture focused on technical excellence and innovation, with a team of experienced professionals.
Provide strategic vision for the clinical research team and generate rigorous evidence to inform Virta's care model and build credibility.
Oversee real-world evidence generation from claims and clinical datasets to demonstrate program impact and drive commercial growth.
Build KOL networks, communicate science, and partner with marketing to translate outcomes into compelling market narratives.
Virta Health is on a mission to reverse metabolic disease in one billion people through innovations in technology, personalized nutrition, and virtual care. The company has raised over $350 million from top-tier investors and partners with the largest health plans and employers.
Manage TMF operations activities for multiple complex studies or sponsor portfolios.
Oversee Trial Master File quality control including planning, tracking, and reporting.
Support regulatory inspections and sponsor audits while collaborating with cross-functional teams.
This is a global clinical research environment focused on ensuring accuracy, compliance, and quality of essential trial documentation. The company operates with a collaborative international team and values inclusion, professional growth, and purpose-driven healthcare work.
Provide physician-level medical oversight for early-phase clinical trials, ensuring participant safety through screening, eligibility review, and real-time clinical decision-making.
Participate in Safety Review Committee meetings and dose-escalation decisions for first-in-human and ascending dose studies.
Review study protocols, informed consent forms, and safety monitoring plans, and serve as medical liaison during audits and inspections.
Celerion is a Contract Research Organization (CRO) specializing in Phase I and early-phase clinical trials, including first-in-human studies. They partner with pharmaceutical and biotechnology sponsors to advance new therapies, and emphasize integrity, trust, teamwork, and respect as core values.