Associate Director, Clinical Scientist, Oncology
USA - Pennsylvania - North Wales (Upper Gwynedd)
Job Description
Job Summary
This position drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate with global, cross-functional team members including clinical directors and study managers to lead/support clinical trial scientific activities.
Job Responsibilities
Responsible for the clinical/scientific execution of clinical protocol(s).
Serves as the lead clinical scientist on the clinical trial team.
Collaborates with the Medical Writer on clinical/scientific and regulatory documents.
Partners with Study Manager on study deliverables.
Participates in the set up and design during study start up (e.g., database set up)
Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with the Clinical Director.
Builds talent and capabilities of direct/indirect team members through proactive coaching, mentoring and development opportunities.
May include management of direct reports including assignment of resources, professional development, and performance management.
May serve as a subject matter expert and/or participate on process improvement teams.
Required experience and skills:
Demonstrated ability to drive and manage scientific activities on clinical.
protocols. This position may represent the company through external partnerships, collaborations, and key strategic engagements. This includes the ability to:
Apply strong knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
Manage multiple competing priorities with good planning, time management and prioritization skills.
Advanced 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, strategic thinking and leadership driving toward study goals.
Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division.
Demonstrated ability to effectively delegate and assign activities to meet the business needs.
Problem solving, prioritization, conflict resolution, and critical thinking skills.
Build team capabilities through proactive coaching.
Advanced communication, technical writing, and presentation skills
Minimum education required:
Bachelor’s degree + 9 years OR Master’s + 6 years OR PhD/PharmD + 2 years
Pharmaceutical and/or clinical drug development experience. Degree in life sciences, preferred.
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 …
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Regions Countries Benefits/Perks SkillsAnalytical Clinical Research Clinical trials Collaboration Communication Critical thinking Design GCP ICH Innovation Leadership Manufacturing Oncology Planning Process Improvement Regulatory requirements Strategic Thinking Technical
Tasks- Coach and mentor team members
- Collaboration
- Interact with key stakeholders
- Problem solving
2 years
EducationBachelor's Business Degree in life sciences Life Sciences Master's Pharm.D Ph.D.
RestrictionsHybrid Hybrid work model
TimezonesAmerica/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