area has an immediate need for a contract based Clinical Site Manager. Role is initially 12 months with... must have 3-5 years of clinical research experience...

management on multiple clinical trials. This position... experience in clinical data management in the pharmaceutical/ biotechnology/ CRO setting. • Knowledge of...

Clinical Data Management department located at our Ridgefield, CT facility. As a Specialist III, Clinical... clinical trial area in developing/managing clinical...

support the Clinical Development Plan. The Sr. CSM will be responsible for ensuring clinical study quality... clinical concepts used to conduct Phase I-IV clinical...

clinical Data Management also carries out the function of a project or trial data manager for a clinical... clinical trial area in developing/managing clinical...

of clinical studies that support the Clinical... of scientific/medical and clinical concepts used to conduct Phase I-IV clinical trials. # Has demonstrated...

of clinical studies that support the Clinical... ensuring clinical study quality/consistency of performance and in conjunction with the Clinical Leader and...

clinical development plans into efficient operational strategies for the optimal delivery of clinical... clinical research and drug development with clinical...

candidates need to come from a CRO or sponsor background in the clinical/pharma space. Labeling experience... direct sponsor and/or cro experience need only apply.

of clinical studies that support the Clinical... ensuring clinical study quality/consistency of performance and in conjunction with the Clinical Leader and...

of biologic portfolio within Clinical Assay Group and participate in clinical program immunogenicity risk... of clinical development. •Contribute to clinical...

of clinical studies that support the Clinical... of scientific/medical and clinical concepts used to conduct Phase I-IV clinical trials. Has demonstrated...

The SrCPRS / CPRS will also liaise with clinical site and CRO staff throughout the study development... Monitor and the Clinical Sites / CRO Support Drug...

contribute outstanding clinical insight with consumer... Previous on-site clinical monitoring experience at a CRO is required 3+ years on-site clinical monitoring...

contribute outstanding clinical insight with consumer... Previous on-site clinical monitoring experience at a CRO is required 5+ years on-site clinical monitoring...

quality clinical study protocols and clinical study... in writing clinical study protocols and clinical study reports • Experience working with clinical...

writer for clinical study protocols. May also serve as principal medical writer for clinical study reports... back to the CRO in the preparation of clinical study...

Assists the clinical monitor and/or medical supervisor in preparing clinical trial protocols, writing non-driven data sections of clinical trial reports and in...

of biologic portfolio within Clinical Assay Group and participate in clinical program immunogenicity risk... of clinical development. ?Contribute to clinical...

firm specializing in Clinical and Scientific... of relevant pharmaceutical industry experience ? Clinical publications planning in Oncology ? PhD ? MS...