Senior Clinical Program Manager - Equity & Bonus Eligible

Supernus Pharmaceuticals, Inc.

Rockville (MD)

Vor Ort

USD 123.000 - 150.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Health
Dental
Vision
Paid time off
401k company match
Company paid life insurance
Health and wellness benefits

Zusammenfassung

Supernus Pharmaceuticals, Inc. is seeking a Clinical Operations Lead to provide leadership, direction, and execution of protocols across clinical programs.

The role requires coordinating with Clinical Research and Operations teams, managing vendors, budgets, and timelines to ensure compliant and timely trials. Ideal candidates will have a BS/BA in a biomedical discipline with 6+ years of clinical operations experience, or an MS with 5+ years (PhD/MD/PharmD/DVM with 3+ years also acceptable).

Qualifikationen

  • Leadership and management of clinical operations projects.
  • Experience planning and oversight of regulatory compliant clinical programs.
  • Strong communication and cross-functional collaboration skills.

Aufgaben

  • Plan and implement clinical trials for assigned programs.
  • Oversee vendor selection and management, including RFPs, timelines, and budgets.
  • Forecast study budgets and collaborate with finance.
  • Serve as Clinical Operations Lead in project team meetings.
  • Ensure compliance with protocol and GCPs.
  • Contribute to development of Target Product Profiles and SOPs.

Kenntnisse

Leadership
Clinical project management
Regulatory knowledge
Verbal & written communication
Independent work

Ausbildung

BS/BA in biomedical discipline
MS in related field
PhD/MD/PharmD/DVM in related field

Jobbeschreibung

Supernus Pharmaceuticals, Inc. is seeking a Clinical Operations Lead to provide leadership, direction, and execution of protocols across clinical programs.

The role requires coordinating with Clinical Research and Operations teams, managing vendors, budgets, and timelines to ensure compliant and timely trials. Ideal candidates will have a BS/BA in a biomedical discipline with 6+ years of clinical operations experience, or an MS with 5+ years (PhD/MD/PharmD/DVM with 3+ years also acceptable).

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