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in Basking Ridge, NJ
Clinical Trial Manager Job - Full-time / Part-time
Hours | Full-time, Part-time |
---|---|
Location | Basking Ridge, NJ Basking Ridge, New Jersey |
About this job
Clinical Trial Manager needed for a Contract opportunity with Yoh's client located in Basking Ridge, New Jersey.
The Big Picture - Top Skills You Should Possess:
- Pharmaceutical
- Logistics
- Clinical Trials
- Oncology
What You'll Be Doing:
- The Clinical Trial Manager provides strategic and operational leadership of clinical research studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs.
- Responsible for the development and management of vendor scope of work (SOW) per contract, quality, and budget.
- Review/approval of vendor invoices and management of accruals and SOW changes.
- Oversight of clinical monitoring quality and adherence to established processes and plans.
- Development, management, maintenance of study deliverables [i.e. timelines, study plans, etc.] through collaboration with internal and external stakeholders using data and strong inter-personal influencing skills to make robust data driven decisions.
- Proactive identification of potential risks and development/implementation of actions to avoid or mitigate and able to make the appropriate trade-offs of balancing risks with study deliverables and costs.
- Maintenance/updating of data as appropriate in project management tools including CTMS.
- Develop, manage, and maintain study deliverables [i.e. timelines, study plans, etc.] through collaboration with internal and external stakeholders using data and strong inter-personal influencing skills to make robust data driven decisions.
- Proactive identification of potential risks and development/implementation of actions to avoid or mitigate and able to make the appropriate trade-offs of balancing risks with study deliverables and costs.
- Maintenance/updating of data as appropriate in project management tools including CTMS.
- Informing operational program lead/s and other leadership (as appropriate) on overall clinical trial plans, updated forecasting, and of potential issues/mitigation.
What You Need to Bring to the Table:
- BA/BS Degree in relevant discipline.
- MINIMUM 4 years clinical study management (directly involved in cross-function team responsible for implementing the protocol) experience including multinational experience.
- Experience in oversight of CRO study execution preferred.
- At least 1 year recent hematology/oncology experience.
- Requirement of MS applications including (but not limited to) MS Project, Word, Excel. Study Tools including electronic system skills - CTMS / EDC.
- Strong leadership skills.
Bonus Points! Otherwise Known As Preferred Qualifications:
- Masters Degree preferred.
What are you waiting for? Apply Now!
Recruiter: Corrin Pyle
Yoh makes finding and applying for jobs simple. Partner with Yoh to find the right opportunities across multiple industries in the US and UK. Find out more !
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. to contact us if you are an individual with a disability and require accommodation in the application process.
J2W: CLINICAL; J2W: SCIENTIFIC; MONJOB
TAX TERM: CON_W2
J2WMIDATL
Ref: 1064694
SFSF: LS