FreshRemote.Work

Clinical Scientist, Oncology

USA - Pennsylvania - North Wales (Upper Gwynedd)

Job Description

This position contributes to the scientific planning and execution of one or more clinical trials. Assists the Lead Clinical Scientist and study team with the scientific conduct of clinical studies. In this position, you will have the opportunity to develop your leadership, technical skills, and scientific acumen as part of a global, cross-functional team.

Job Responsibilities

  • Responsible for specific clinical/scientific activities on a single study or across multiple studies (e.g., medical monitoring, lab specimen tracking/reconciliation, adjudication support, preparation of meeting materials).

  • Support development of Protocol and related study materials (e.g., ICF documents/amendments, data management deliverables).

  • May interact with internal and external stakeholders (e.g., country operations, committees, vendors) in support of clinical study objectives.

  • Support development of site and CRA training materials

  • Prepare clinical narratives

  • Collaborate cross-functionally to monitor clinical study data to ensure quality, completeness, and integrity of trial conduct.

  • Participate in CRF design to ensures data collection is in alignment with the protocol.

Core Skills

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

  • Ability to manage multi e competing priorities with good planning, time management and prioritization skills

  • Analytical skills with the ability to interpret clinical trial data and synthesize conclusions

  • Interact with key stakeholders across department, division, and company. Role requires a proactive approach in driving toward study goals.

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

  • Solid communication, technical writing, and presentation skills


Education/Experience

  • Bachelor's Degree +2 years of pharmaceutical, clinical drug development, project management, and/or medical field experience

  • OR Master's Degree +1 year of pharmaceutical, clinical drug development, project management, and/or medical field experience

  • Degree in life sciences, preferred.

MRLGCTO

CSSMHiring

#eligibleforerp

CSSMOncology

NOTICE FOR INTERNAL APPLICANTS

In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.

If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.

Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based …

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Job Profile

Restrictions

Hybrid Hybrid work Hybrid work model

Benefits/Perks

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

Tasks
  • Collaborate cross-functionally
  • Collaboration
  • Communication
  • Conflict resolution
  • Data Collection
  • Data Management
  • Innovation
  • Leadership
  • Planning
  • Presentation
  • Prioritization
  • Problem solving
  • Project management
  • Technical writing
Skills

Analytical Business Operations Clinical Clinical Research Clinical trials Collaboration Commercial Communication Conflict Resolution Critical thinking Data Data Collection Data Management Design Drug Development Execution GCP ICH Inclusion Innovation Leadership Management Manufacturing Medical Medical Monitoring Monitoring Oncology Pharmaceutical Planning Presentation Prioritization Problem-solving Project Management Quality Regulatory Regulatory requirements Research Scientific Acumen Talent Acquisition Technical Technical Writing Time Management Training Writing

Experience

1-2 years

Education

Bachelor's Bachelor's degree Business Life Sciences Management Master's Master's degree Oncology

Timezones

America/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Europe/London Pacific/Honolulu UTC+0 UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9