Director/Senior Director, Clinical Development

Description

Why join Cardurion Pharma?
At Cardurion, we are advancing the understanding of the cellular mechanisms that regulate heart function and are developing new treatments to address cardiovascular disease. Our programs seek to modulate signaling pathways that regulate heart cell function to reverse the pathophysiological mechanisms that drive cardiovascular disease. We invite you to explore our site to learn more about our Company and how we are advancing the promise of cardiovascular signaling pathways science to improve health and impact lives around the world.

The Role
Cardurion is seeking a biopharma physician-scientist with a strong background in Cardiovascular Clinical Development to join the team. This person will report directly to the Clinical Development Lead of one of our exciting programs.  
Here's What You'll Do Contribute to clinical plans, trial design, and clinical trial execution, serving as a clinical expert to internal and external collaborators, investigators and other stakeholders.  Represent the clinical development functions on various cross functional teamsCollaborate on integrated development plans and work with support functions to ensure full integration of the development strategy for each assetAuthor clinically-relevant sections of regulatory documentsCo-authors manuscripts, abstracts, and when/ where possible present clinical research results at scientific congresses, including internally-organized events such as clinical and scientific advisory board meetings and clinical trial investigator meetings Participates in select data monitoring committee (DMC), safety review committee (SRC), and other clinical trial oversight committees, defined within clinical trial protocols.In conjunction with development operations, drafts charters for oversight committeesInforms site selections and collaborations with key investigatorsTracks and ensures any concerns regarding study participant safety are addressedProactively addresses any topics that may impact clinical trial integrity Perform clinical review of data listings and essential study data within generated statistical reports (eg, SAS outputs) and other available data surveillance tools (eg, Spotfire, Rave) and partner with Data Management in generating relevant queries Liase among clinical trial innovators and Cardurion Support business development and investor relations activitiesHere's What We'll Bring To The Table Highly competitive healthcare coverage including: medical offered through BCBS (HMO/PPO), Delta Dental, and vision offered through VSPFully funded HSA for high-deductible PPO PlanFlexible Spending Accounts for medical expenses and dependent care expenses4 weeks Paid Time Off annually 401k (traditional and Roth offered) with 50% match on first 4% deferred. Match is vested immediatelyA suite of Cardurion paid insurance coverage, including: life insurance, short-term and long-term disability10 company paid holidays and Year-End shut down Our Mission

Translate our world-class expertise in cardiovascular signaling pathways into groundbreaking therapeutics for patients.

Cardurion is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Cardurion will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.  Requirements

Here's What You'll Bring To The Table MD, DO (or equivalent degree(s)) requiredFellowship training in cardiology or related subspecialty is required, and additional clinical practice is preferred  >2 years of experience in clinical development in pharma, biotech, and/or CROEvidence of strong writing and presentation skills is required Strong working knowledge of global clinical trial regulations and best practicesWillingness to travel domestically and internationally (expect 15% travel)Strong team facilitation skillsExcellent written and oral communicationsComfortable presenting to internal and broad external audiencesEffectively anticipates challenges and proactively addresses themCan manage and prioritize multiple activitiesWorks well in a highly matrixed environment as would be expected in a biotech companyCan influence peers and external partners very effectively