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| Job #02224 |
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| About our client |
| Our client is a full service Contract Research Organization (CRO) offering a suite of clinical trial management services from initial study design to final regulatory submissions. The company has successfully completed clinical validation studies in the United States, Africa, Europe, Asia, and South America and offers a full ‘turnkey’ approach to outsourcing such studies. It has the ability to rapidly identify the most significant and rare global patient populations and decrease the time taken for marketing products. |
| Position |
Location |
| Director of Clinical Research Services |
Florida |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Manage clinical research project 2) Work with a team of CRAs and clinical assistants 3) Maintain IVD patient collections for trials, but expanding into biopharma 4) Develop and maintain database of PI's 5) Organize team to work more effectively toward goals 6) Maintain SOPs and work with consultants 7) Generate and maintain internal budgets 8) Interact with staff as liaison for CRS (Clinical Research Services) Department 9) Maintain communication flow, project budgeting, timeline development, CRF, ICF, and protocol development |
| Requirements |
1) Degree, CCRC a plus 2) Minimum 5 years experience in IVD and/or biopharmaceuticals 3) IVD trial experience a plus 4) Management experience highly preferred 5) In-depth knowledge of GCP, HIPAA, ICF, CRF protocols, and ICH 6) Ability to recruit sites as required for trial population requirements |

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