Collabera
Overview
Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs.
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence.
Job Description
Minimum of 3 to 5 years of pharmaceuticals/biotech experience.
Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials.
Process and system thinking, customer orientation, and ability to work in multidisciplinary study teams and to execute within a matrix management model, ideally in pharmaceuticals/biotech.
Experience in execution of clinical research trials, including GCP and regulatory guideline knowledge and audit inspections.
Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics.
Demonstrated ability to support the development and management of various aspects of the end to end study operational plan.
Demonstrated ability to support the operational execution and delivery of various aspects of a quality clinical trial.
Demonstrated experience in change management initiatives preferred.
Program and project management experience preferred.
Qualifications Responsible for supporting the Senior Clinical Trial Manager/operational study lead, and for managing various aspects of the operational execution and delivery of quality studies, including in process quality control activities (e.g. quality checks and balances to ensure inspection readiness, Enrollment, Metrics, Milestones, Timelines and Budget).
Additional Information All your information will be kept confidential according to EEO guidelines.
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Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence.
Job Description
Minimum of 3 to 5 years of pharmaceuticals/biotech experience.
Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials.
Process and system thinking, customer orientation, and ability to work in multidisciplinary study teams and to execute within a matrix management model, ideally in pharmaceuticals/biotech.
Experience in execution of clinical research trials, including GCP and regulatory guideline knowledge and audit inspections.
Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics.
Demonstrated ability to support the development and management of various aspects of the end to end study operational plan.
Demonstrated ability to support the operational execution and delivery of various aspects of a quality clinical trial.
Demonstrated experience in change management initiatives preferred.
Program and project management experience preferred.
Qualifications Responsible for supporting the Senior Clinical Trial Manager/operational study lead, and for managing various aspects of the operational execution and delivery of quality studies, including in process quality control activities (e.g. quality checks and balances to ensure inspection readiness, Enrollment, Metrics, Milestones, Timelines and Budget).
Additional Information All your information will be kept confidential according to EEO guidelines.
#J-18808-Ljbffr