Yochana IT Solutions Inc
Yochana IT Solutions Inc. specializes in creating custom-matched connections between professionals and companies in temporary, contract-to-hire, direct hire and retained positions. We provide staffing & industry-specific solutions for hiring with confidence.
Job Description
We are seeking a
Project Manager/BA
for a position in
Princeton, NJ
with a duration of
6-12 months . Note: Only Green Card or Citizens local to New Jersey are eligible. Job Requirements: 9-11 years of experience in a pharmaceutical company/CRO with business analyst along with project management Strong understanding/knowledge on clinical research and development area with regulatory documentation Should be aware of end to end clinical business and technical process Understanding of various business groups and their functions tied to clinical drug development Experience to understand and come up plan to fill the gap between business process and technologists Strong understanding of clinical, data management, safety and regulatory IT systems such as CDMS (EDC), CTMS, eTMF, RBM, IVRS, Safety, Regulatory submission and publishing systems Experience in end-to-end (full service) clinical trials management, ideally with project management relevant clinical research experience Ability to understand large complex processes with a focus on continuous improvement Strong technical writing skills and analytical skills Qualifications
Need Program Manager with CRO experience and experience working with Pharmaceutical and Clinical clients. Additional Information
If your skills and experience match the above job description, please contact us at 248-507-4056.
#J-18808-Ljbffr
We are seeking a
Project Manager/BA
for a position in
Princeton, NJ
with a duration of
6-12 months . Note: Only Green Card or Citizens local to New Jersey are eligible. Job Requirements: 9-11 years of experience in a pharmaceutical company/CRO with business analyst along with project management Strong understanding/knowledge on clinical research and development area with regulatory documentation Should be aware of end to end clinical business and technical process Understanding of various business groups and their functions tied to clinical drug development Experience to understand and come up plan to fill the gap between business process and technologists Strong understanding of clinical, data management, safety and regulatory IT systems such as CDMS (EDC), CTMS, eTMF, RBM, IVRS, Safety, Regulatory submission and publishing systems Experience in end-to-end (full service) clinical trials management, ideally with project management relevant clinical research experience Ability to understand large complex processes with a focus on continuous improvement Strong technical writing skills and analytical skills Qualifications
Need Program Manager with CRO experience and experience working with Pharmaceutical and Clinical clients. Additional Information
If your skills and experience match the above job description, please contact us at 248-507-4056.
#J-18808-Ljbffr