AD/Director Clinical Development

184922
  • 200000 USD - 300000 USD
  • San Francisco, United States
  • Permanent

Join a forward-thinking organization at the forefront of innovative therapies in the life sciences sector. This is a unique opportunity to play a key role in driving clinical development for groundbreaking treatments, making a tangible difference in patients’ lives while progressing your career within a collaborative and dynamic environment. If you’re passionate about leading clinical studies that push the boundaries of science, this role offers the platform for you to shine.

Our client is a growing company specializing in advancing therapies in immunology, dermatology, and related fields. They support scientific innovation and are committed to delivering impactful solutions for complex health conditions. In this role as a senior-level professional, you will lead pivotal phase 3 clinical development programs, shaping the future of their pipeline and ensuring scientific excellence in every step.

Role Summary:
You will oversee the clinical development and execution of global phase 3 trials, working closely with a cross-functional team of scientists and clinicians. Your expertise will guide the scientific design and operationalization of studies, contributing to the organization’s broader mission of developing transformative treatments. This position can be fully remote with biannual on-site meetings, offering flexibility and a chance to influence global studies from anywhere.

Key Responsibilities:

  • Lead the planning, execution, and management of late-stage clinical trials, ensuring alignment with regulatory standards and organizational goals.
  • Manage multidisciplinary teams, providing scientific input and strategic guidance throughout the trial lifecycle.
  • Support protocol development and clinical buildouts, ensuring studies are scientifically robust and feasible.
  • Collaborate with CROs and external partners to ensure smooth trial operations and adherence to timelines.
  • Deliver scientific presentations and contribute to thought leadership within the organization.
  • Drive compliance, quality standards, and data integrity across all clinical activities.

Experience & Requirements:

  • PhD, PharmD, or equivalent in a relevant scientific discipline with 6-10 years of clinical research experience.
  • Prior experience overseeing phase 3 trials in immunology, dermatology, or oncology, preferably with global study exposure.
  • Strong knowledge of clinical trial processes, regulatory guidelines, and scientific strategy.
  • Excellent communication skills capable of presenting complex scientific data clearly and effectively.
  • Experience working in cross-functional teams and managing external partners/CROs.

This role offers a base salary between $200,000 and $300,000, depending on experience.

Apply now to be part of a growing team shaping the future of innovative therapeutics.


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