Clinical Trial - Project Coordinator II

This position works closely with other Biomarker operation Project Managers and be based at either the Rahway NJ or Upper Gwynedd PA Client site.

Project Coordinator, Integrated Biomarker Operations

Qualifications:
Required Experience and Skills:
BA/BS/Master's in a scientific or technical field of study with 2-5years 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
Team player

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

Preferred Experience and Skills:
2 years experience working in a clinical trial operation.
Formal Project Management Training.
Experience with SharePoint.

*Note*:
2 year assignment
Hybrid role (any 2days/onsite).
Work location option: Rahway, NJ OR Upper Gwynedd PA.
Can consider Master's candidate with no more than 5 years of relevant experience.
Willing to look at Clinical Operation experience within university , but industry expertise is highly preferred.
TA: Oncology is preferred, will consider immunology operations study experience as well.
Do not submit candidates with patient recuitment, site management and sample testing experience with clinical trial or lab for this role.
Do not submit PHD candidates for this role.

Previous experience that will be preferred/good fit for the role:
Project management/coordination within clinical trial study/clinical research
Clinical trial operations.
Biomarkers experience

Responsibilities:
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 Client 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.