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Clinical Operations Assoc. Director, Clinical Trial Educator

External
bridgebio logoBridgebio · Remote
Full-timeRemoteToday
Clinical TrialsComplianceGCP
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Responsibilities

  • Maintains clinical knowledge of the therapeutic area landscape including current treatment strategies, current and pending competitors, and new therapeutic developments.
  • Establishes and maintains collaborative relationships with key therapeutic area experts, investigators, and institutions, serving as a key Eidos contact for investigative sites.
  • Collaborates with clinical development and operational teams, as well external service providers as appropriate to coordinate and optimize educational and research support for sites/investigators participating in BBIO's clinical trials, creating and contributing to study documents as needed.
  • Provides ongoing evaluation of enrollment status by site to ensure they are meeting expected goals, as well as patient compliance and study completion.
  • Provides white glove experience and oversight of key study procedures procedure periods with identified needs, such as screening, working with sites to ensure understanding and guide through the process as needed.
  • As requested, participates in medical education for healthcare professionals through presentations and investigator interactions such as investigator meetings and other appropriate venues to enhance product and disease state knowledge.
  • May assist in CRA monitoring oversight as needed.
  • Where You'll Work
  • This is a U.S.-based remote role that will require periodic visits to our San Francisco Office.

Requirements

  • Historically the "Experience, Education, & Skills Requirement" section
  • (5-7 bullets max)
  • BA/BS or MA/MS in biological or medical field required or relevant experience; advanced degree or clinical background preferred.
  • Minimum of 10 years of relevant clinical experience in the pharmaceutical, biotech and/or CRO industries, with at least 5 years of experience in a similar role.
  • Strong interpersonal skills and excellent relationship-building skills
  • In-depth Knowledge of FDA regulations, GCP, GCDMP and ICH guidelines required.
  • Clear scientific curiosity and interest in drug development
  • Strong verbal and written communication skills
  • Passion for helping patients.
  • Identifies and applies advanced practices, technical principles, theories and/or concepts, and contributes to the development of new principles and concepts; has a comprehensive understanding of current approaches in industry and ability to incorporate them into Eidos' programs.
  • Travel- 20%
  • At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will wor

Benefits

Health insuranceRemote work optionsEquity / stock optionsPerformance bonus

Additional Information

Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a "moneyball for biotech" approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation-including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work.


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