Clinical Trial Manager 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 [ie 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 [ie 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, a DayJ2W: SCIENTIFIC; MONJOB

TAX TERM: CON_W2J2WMIDATL

Ref:

SFSF: LS