Project Coordinator - Rahway, United States - Spectraforce Technologies

Description

Project Coordinator - Integrated Biomarker Operations

Rahway, NJ 07065

23 Months

Notes

• 2 year assignment
• Hybrid role (any 2days/onsite).
• Work location: Rahway,NJ OR WestPoint,PA.

Previous experience that will be preferred/good fit for the role:

• Project management/coordination with in clinical trial study/clinical research
• Clinical trial operations
• Biomarkers experience

Qualifications:

Required Experience and Skills:

• Minimum: BA/BS in a scientific or technical field of study with 2 years experience within clinical trial.
• Good team working skills within a clinical trial environment.
• Excellent attention to detail and organizational skills
• Strong written and oral communication skills
• People person and Team player

Software skills: MS office and advanced excel, work experience with sharepoint.


Preferred Experience and Skills:

• 2 years' experience working in clinical trial operation
• Formal Project Management Training
• Experience with SharePoint.

Responsibilities:
Seeking a Project Coordinator to provide project and document management support for the Integrated Biomarker Operations group. He/She will ensure timely and accurate deliverables in accordance with rigorous scientific and ethical standards.

This position works closely with other Biomarker operation Project Managers and be based at either the Rahway NJ or West Point PA Merck site.

Primary activities include, but are not limited to:

• Support Project Managers by coordinating and overseeing all biomarker operation activities required to manage the life cycle of Biomarker sample (collection, processing, analysis, data delivery & final sample disposition)
• Loading and tracking logistics related documentation in internal Project Management Information Systems.
• Proactively monitor project timeline to assist coordination of activities that help prepare project team to achieve key milestones.
• Maintain effective communication and working relationships with project team members, and other internal Merck teams.
• Ability to understand and resolve conflicting needs of key stakeholders.
• Contribute to process improvement identification and implementation efforts.
• Support multiple projects across various clinical trials.
• General project management support as needed.