Clinical Operations Associate (Remote) Job at Tandym Group
A New Jersey-based pharmaceutical company is currently seeking a new Clinical Operations Associate for a promising Remote opportunity with their growing staff. In this role, the Clinical Operations Associate (Remote) will be responsible for execution of assigned clinical operations activities in support of study conduct throughout the study lifecycle and ensuring quality execution and compliance with all required policies and procedures in completion of assigned tasks.
Responsibilities:
The Clinical Operations Associate (Remote) will
Responsibilities:
The Clinical Operations Associate (Remote) will
- Assist with resource acquisition & allocation activities
- Assist with clinical audit/inspection activities as assigned
- Participate in the development, review, implementation and updating of key standard processes that lead to positive and measurable impact for clinical programs managed by the Clinical Management team
- Assist with management of clinical systems updates, enhancements and master data stewardship as required
- Support coordination of project activities and liaise between global affiliates, external vendors, and clinical research teams as requested
- Serve as a resource to departmental personnel and external service providers in areas of expertise including applicable internal database and electronic systems applications and process management
- Assist with the management of ESP counterparts and processes for vendors / external service providers / contract personnel implementing program level activities
- Support with tracking and reporting of Key Performance Indicators (KPIs) and metrics for quality oversight of applicable clinical operations related activities, as assigned
- Collaborate/Interact with internal and external stakeholders as related to conduct of required job responsibilities
- Perform other duties, as needed
- 2+ years of related work experience
- High School Diploma / GED
- Knowledge of ICH/GCP, local regulatory authority drug research and development regulations and Clinical Trial Operations
- Clinical Trials Support and/or Pharmaceutical industry experience
- Computer savvy
- Microsoft Office Suite proficient
- Great interpersonal skills
- Excellent communication skills (written and verbal)
- Strong atteniton to detail
- Highly organized
- Bachelor’s Degree
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