Oversee clinical data management activities across complex research studies from start-up to database lock.
Act as primary data management subject matter expert and client-facing representative.
Lead cross-functional collaboration with clinical operations, statistical programming, and biometrics teams.
The partner company focuses on clinical research and data management to advance healthcare. They offer a collaborative remote environment with a focus on operational excellence.
Accountable for translational development strategy from drug candidate through IND submission and Phase 1 entry.
Support biomarker strategies, indication selection, and patient stratification to guide program decisions.
Lead IND-enabling activities, author regulatory documents, and serve as translational science lead in FDA interactions.
We are a small, driven biotech company using Nobel Prize-winning click chemistry to develop targeted cancer therapies that activate potent drugs only at the tumor site. We are a remote-first team encompassing broad backgrounds, united by a mission to make cancer treatments more effective with minimal side effects.
Define and drive the global medical affairs strategy across investigational and marketed products in a fast-growing biotech environment.
Build, lead, and scale the global medical affairs organization, including hiring, mentoring, and developing high-performing teams.
Provide strategic medical leadership to cross-functional teams and oversee clinical research, publication strategy, and scientific communications.
Our partner is a rapidly growing biotech organization. They operate in a highly dynamic and entrepreneurial environment, balancing long-term vision with urgent execution.
Provide advisory on clinical development analytics, leveraging 10+ years of pharma experience.
Lead adoption of data tools and dashboards across clinical development teams.
Translate between data engineering and clinical stakeholders to optimize drug development data.
Edison Scientific is a biotech and pharma analytics firm focused on clinical development data. They offer a mission-driven culture with regular team offsites and a fast-moving environment.
Conduct and report SIV, RMV, COV onsite monitoring visits and perform CRF review, source document verification, and query resolution.
Manage site communication and be the point of contact for in-house support services and vendors, while communicating with internal project teams on study progress.
Support regulatory teams in preparing documents for study submissions and prepare for and participate in audits and inspections.
The company is a dynamic, global mid-size clinical research organization founded in 1995, bringing together more than 3,000 dedicated individuals. They work on the frontline of medical science, changing lives and bringing new medicines to those who need them.