Celcuity

7 open remote positions

Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies for the treatment of multiple solid tumor indications. The company was founded to develop a better way to treat the cellular drivers of tumor growth.

Salary Distribution 7 of 7 jobs

Benefits Overview 7 of 7 jobs

401(k) (7) Dental (7) Medical (7) PTO (7) Vision (7) Equity (1)

Open Positions

$230,000–$275,000/yr

  • Identify and cultivate professional relationships with KOLs in designated tumor types.
  • Maintain cross-functional field partnerships allowing for appropriate collaboration with field commercial teams.
  • Develop scientific expertise on all Celcuity’s products, related disease states, and the clinical practice for a given therapeutic area.

$190,000–$220,000/yr

  • Support Safety Physicians with safety-related tasks across commercial products and products in clinical development.
  • Contribute to safety risk management including but not limited to routine review of safety data and pertinent scientific literature articles.
  • Conduct signal detection activities and analyses of safety data to support appropriate benefit-risk assessment as directed by the Safety Physician.

$150,000–$190,000/yr

  • Lead the monthly, quarterly, and annual financial close processes to ensure timely and accurate reporting in accordance with US GAAP.
  • Manage complex accounting areas, including revenue recognition and gross-to-net estimates, equity compensation, collaboration agreements, and equity and debt financing.
  • Drive the design, implementation, and maintenance of robust internal control procedures to mitigate financial reporting risks.

$220,000–$270,000/yr

  • Oversee end-to-end ICSR collection, processing, reconciliation, and reporting of post-marketing cases.
  • Ensure global compliance with pharmacovigilance regulations, including timely ICSR submission, high-quality case processing, and support for aggregate reporting.
  • Provide oversight and support of the PV vendor activities, including but not limited to the establishment and monitoring key performance indicators (KPIs) and vendor audits.

$260,000–$350,000/yr

  • Assist in design, author and/or review clinical study synopses, protocols, study reports and other study-related documents.
  • Act as a medical monitor for assigned study and discuss study design with investigators and key opinion leaders.
  • Track emerging efficacy and safety profile of drugs in clinical trials; inform Clinical Development team of changes in the efficacy/safety profiles.