Duties and Responsibilities:
Scope of responsibilities include, but are not limited, to the following:
Support communication between clients and the Company;
- Manage and monitor client projects including sample preparation, testing, biorepository and reporting activities such that they are completed in a timely fashion, in accordance with Company SOPs and per client agreements.
- Work with other functional areas to develop and implement project plans and obtain resources to successfully achieve milestones and high levels of client satisfaction.
- Proactively manage and drive the resolution of client issues.
- Draft study plans, final reports and other documents as required.
Competencies:
- Strong organizational skills and attention to detail
- Ability to communicate effectively both orally and in writing
- Problem-solving skills
- Ability to prioritize completing tasks
- Customer-focused attitude
- Ability to facilitate meetings, record meeting minutes, record action items and follow-up on pending activities
- Strong time management skills
- Ability to work well on an independent basis
- Commitment to detailed record-keeping in compliance with all regulatory requirements
- Proficiency in MS Project, Word, Excel and PowerPoint
- Strong analytical and critical-thinking skills
- Working knowledge of pharmaceutical services or life science project management or project monitoring
Qualifications:
- Degree in biological sciences; Master’s Degree in a relevant discipline a plus
- Three plus years clinical research and/or laboratory experience in the molecular diagnostic industry; Oncology knowledge a plus
- Experience monitoring or coordinating pharmaceutical research or pharmaceutical services projects;
- Knowledge of data quality control and bioanalytical study record keeping
- Working knowledge of GLP and GCLP
Interpace Pharma Solutions is an Equal Opportunity and Affirmative Action Company
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