767 Oracle jobs in Spring Mount, PA
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      Director, Regulatory Program Management & Submission Strategy (Oncology)

      Pfizer

      Collegeville, PA 19426

      Hybrid~ 14 minHealth InsurancePaid Time OffRetirement Benefit

      • 10 or more years of relevant experience
      • Mastery of program management skills and significant expertise in drug development
      • Experience leading the planning and execution of major regulatory submissions (e.g. NDA/BLA/MAA) is required
      • Bachelor's degree in one of the disciplines related to drug development or business required
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      Community Recruiter

      Pennsburg Manor

      Pennsburg, PA 18073

      $75,000/yr
      Requires TravelUrgently HiringEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

      • At least 2-4 years of experience in recruitment, talent acquisition, or community outreach
      • Valid driver's license and reliable transportation
      • Bachelor's degree in Human Resources, Business Administration, or related field (or equivalent experience)
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      Earn At Least $2310 For Your First 192 Trips, Guaranteed.

      Uber

      Harleysville, PA 19438

      ~ 15 min OnsiteFlexible Schedule

      • A valid U.S. driver's license and vehicle insurance
      • 21 years old or older
      • A 4-door vehicle
      • At least one year of driving experience in the U.S. (3 years if you're under 23 years old)
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      Associate Director, Regulatory Affairs (Remote)

      Jazz Pharmaceuticals

      Philadelphia, PA 19103

      RemoteHealth InsurancePaid Time OffRetirement Benefit

      • Evaluative, analytical and interpretative skills enabling review and synthesis of reports and other documents used in regulatory planning and submissions
      • Proven track record of effective collaboration with regulatory agencies, including FDA, EMA, and PMDA
      • Ability to work with limited supervision, to set priorities to meet timelines and to motivate and influence others
      • Demonstrated leadership success in management of regulatory activities
      • A minimum of 8 years in roles of increasingly responsible in regulatory affairs or related areas in pharmaceutical drug development
      • Deep and broad knowledge of regulatory affairs; direct experience with pharmaceutical regulatory submissions and product approvals
      • Excellent verbal and written communication skills
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