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| Job #03052 |
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| About our client |
| Our client is an international pharmaceutical company with over 20,000 employees. They are leaders in the development and commercialization of therapeutics in a variety of indications. The company is well known for high-quality standards and commitment to innovation. |
| Position |
Location |
| Project Manager |
Pennsylvania |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Oversee clinical study management 2) Handle the setting up and validation of clinical software database, trial monitoring and closeout 3) Participate in Investigator, monitor or client meetings 4) Ensure that design, implementation and timelines of study deliverables are consistent with client and budget expectations 5) Communicate and coordinate timelines for internal and external functional units 6) Coordinate resources and resolve conflict 7) Participate in and lead process improvement initiatives |
| Requirements |
1) BS in Life Sciences or a related field 2) 7+ years of clinical research or related experience 3) 3+ years of experience as a Project Manager (clinical) 4) Experience in a key CRO/pharmaceutical operational function (e.g., data management, clinical operations, laboratory and pre-clinical) 5) Experience in oncology
6) Phase II – IV management experience preferred 7) Experience in resource and budget/financial management
8) Knowledge of clinical study guidelines (FDA, ICH and GCP) 9) In-depth understanding of the clinical trials process 10) Excellent communication skills (written and oral) 11) Good client management skills 12) Proficiency in computers/technology (MS Excel, PowerPoint and MS Project as well as similar project management tools) |

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