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Associate Director, Study Manager - Oncology - Rahway New Jersey
Company: MSD Malaysia Location: Rahway, New Jersey
Posted On: 05/03/2024
Associate Director, Study Manager - Oncology page is loaded Associate Director, Study Manager - Oncology Apply remote type Hybrid locations USA - Pennsylvania - North Wales (Upper Gwynedd) USA - New Jersey - Rahway time type Full time posted on Posted 2 Days Ago job requisition id R289334 Job DescriptionThis position participates in the strategy and leads the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to demonstrate your advanced leadership and technical skills as part of a global, cross-functional team. You will build and coach your team in the development of project management, communication, and collaboration skills in support of our clinical trials.Job Responsibilities - Responsible for the operational planning, feasibility, execution and conduct of clinical trial(s).
- Serves as the Clinical Trial Team lead
- Leads and directs teams in key study planning, development, and execution elements (e.g. operational reviews, issue escalation/mitigations, presentations at Sr. Management meetings, program level cross functional meetings and governance).
- Responsible for facilitating and collaborating with key internal/external stakeholders (study team, subsidiary country teams, vendors, committees, etc.) in support of clinical trial objectives.
- Liaises with partners, vendors, and vendor management team.
- Review and provide clinical operations input into relevant clinical documents such as the protocol and other documents as appropriate.
- May serve as a subject matter expert and/or participate on process improvement teams.
- Builds talent and capabilities of junior team members through proactive coaching, mentoring and development opportunities.
- May include management of direct/indirect reports including assignment of resources, professional development, and performance managementCore Skills
- Strong knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
- Proven ability to manage competing priorities and effectively delegate and assign activities to meet the business needs
- Ability to develop short and mid-range project plans that are realistic and effective at meeting goals.
- Strong analytical skills to drive operational milestones
- Influence opinions and decisions of internal and external customers/vendors, across functional areas, and within the division
- Interact with key stakeholders across department, division, and company. Roles requires a proactive approach, strategic thinking and leadership driving toward study goals.
- Demonstrated leadership skills in programs & processes, leading meetings and influencing peers and direct/indirect reports in a matrix environment.
- Problem solving, prioritization, conflict resolution, and critical thinking skills
- Strong communication, writing, and presentation skills
- Proficient knowledge in Microsoft office or similar (Excel, PowerPoint, Word, Outlook, etc.)Experience
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