- Manages multiple clients and their associated projects, fostering relationships with assigned clientele
- Confirms each project’s scope in conjunction with the client and operational teams to ensure adherence to contractual scope, timelines and budget for all team members
- Engages assigned team and functional managers in the development, assignment and prioritization of work based on the project’s needs, taking corrective action with Operations as appropriate to control project scope and cost
- Fosters high-level of communication by conducting frequent project meetings, initiated at project inception and continuing through project closeout
- Creates or reviews and maintains project-related documentation including: RFIs, Budgets, Meeting Minutes, Timelines, Client Isms, Issues and Risk Lists, Change Requests, etc.
- Implements change management where appropriate to alleviate bottlenecks, improving processes and procedures to enhance the efficiency and effectiveness of the organization
- Updates relevant databases required to maintain and report on current project statuses and overall financial reporting
- Hosts client visits and conducts facility tours
Requirements:
- Bachelor’s degree required (degree emphasis in life science discipline preferred)
- Requires high-level skills in the areas of organization, multi-tasking, relationship-building, communication, judgment, problem-solving, persuading and negotiating
- Minimum 2 years of Clinical Research industry experience is highly preferred
- Phase I Project Management experience preferred
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Skills Required
- Bachelor's degree
- Degree emphasis in a life science discipline
- High-level organizational, multitasking, relationship-building, communication, judgment, problem-solving, persuasion, and negotiation skills
- Minimum 2 years of clinical research industry experience
- Phase I project management experience
What We Do
Celerion, a leader in early clinical research, delivers Applied Translational Medicine. Celerion applies our expertise and experience to translating information gained in research discoveries, to knowledge of drug action and effect in humans to support early drug development decisions and the clinical pharmacology labeling of new medicines. With over 50 years of experience and 600 global clinic beds (including 24 in-hospital), Celerion conducts and analyzes First-in-Human, clinical proof-of-concept, cardiovascular safety (TQT, robust QT), ADME and NDA-enabling clinical pharmacology studies. Celerion provides expertise on modeling and simulation, study design, medical writing (protocols and reports), clinical data sciences, biostatistics, and PK/PD analysis as well as small and large molecule bioanalytical assays through clinical drug development. Regulatory, drug development and program management complement Celerion’s service offerings. Our operations are strategically located in: Lincoln, Nebraska (Corporate Headquarters) Philadelphia, Pennsylvania Phoenix, Arizona Belfast, Northern Ireland,UK Zurich, Switzerland Vienna, Austria Richmond, Virginia Montreal, Quebec, Canada For more information, visit: www.celerion.com
