FreshRemote.Work

Senior Clinical Scientist - Oncology

USA - New Jersey - Rahway, United States

Job Description

This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team.

 

Job Responsibilities:

Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s). This may include:

  • Serving as the lead clinical scientist on the clinical trial team.

  • Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director.

Job Description:

  • This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team.

 

Minimum education required:

  • Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience or Master's Degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical field experience or PhD/PharmD Degree

 

Required experience and skills:

Required/Preferred experience and Skills

  • Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience or Master's Degree +3 year of pharmaceutical, clinical drug development, project management, and/or medical field experience or PhD/PharmD Degree

  • Degree in life sciences preferred

  • Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)

  • Proactive, strategic thinking and leadership in driving toward study goals.

  • Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division

  • Apply leadership skills to processes, leading meetings, and influencing peers in a matrix environment.

  • Problem solving, prioritization, conflict resolution, and critical thinking skills

  • Strong communication, technical writing, and presentation skills

 

ResearchandDevelopmentGCTO

CSSMHir

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. For more information about personal rights under the U.S. Equal Opportunity Employment …

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Job Profile

Regions

North America

Countries

United States

Restrictions

Hybrid Hybrid work Hybrid work model On-site Puerto Rico residents only US and Puerto Rico residents only

Benefits/Perks

Accommodation support Bonus eligibility Diverse environment Diverse workplace Equal opportunity Equal opportunity employer Flexible work Flexible work arrangements Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Inclusive workplace Insurance Meetings Paid holidays Retirement benefits Sick Days Vacation

Tasks
  • Communication
  • Compliance
  • Conflict resolution
  • Execution
  • Innovation
  • Lead clinical trials
  • Leadership
  • Planning
  • Presentation
  • Prioritization
  • Problem solving
  • Project management
  • Technical writing
Skills

Clinical Clinical Research Clinical trials Communication Compliance Conflict Resolution Critical thinking Data Development Deviations Drug Development Education Execution GCP ICH Inclusion Influence Influencing Innovation Leadership Life sciences Management Manufacturing Matrix Environment Medical Medical Monitoring Monitoring Oncology Organization Pharmaceutical PharmD PhD Planning Presentation Prioritization Problem-solving Project Management Protocols Regulatory Regulatory requirements Research Scientific Acumen Strategic Thinking Technical Technical Writing Writing

Experience

5 years

Education

AS Bachelor Bachelor's Bachelor's degree Business Degree Degree in life sciences Development Health Care Life Sciences Management Master Master's Master's degree Oncology Pharm.D Ph.D. Project Management

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9