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inVentiv Health
Clinical Development Associate
Primary Duties:
The Clinical Development Associate will be responsible for partnering with the cross-functional study team to develop the clinical strategy/plan that leads the study team in the execution of clinical trials within the clinical plan. This role will also be responsible for supporting non-trial, trial and project level assignments within the team. The ability to ensure quality on-time fulfillment of deliverables is essential for this position.
Minimum Requirements:
" Three years of clinical research experience.
" Proficient use of Project Management tools such as MS Project.
" Prior project management experience creating project scope, timelines, cost management, quality management, communication plan, risk assessments and contingency planning.
" Previous experience leading cross-functional and cross-cultural teams or projects.
" Knowledge of regulations and guidelines that apply to conduct of clinical trials.
" Strong communication, leadership and networking skills.
" Strong self-management and organizational skills.
" Demonstrated problem solving abilities.
Apply:
For faster processing, please apply online and directly to the employer. Specific instructions on how to apply are available. (recommended)
Clinical Development Associate
Primary Duties:
The Clinical Development Associate will be responsible for partnering with the cross-functional study team to develop the clinical strategy/plan that leads the study team in the execution of clinical trials within the clinical plan. This role will also be responsible for supporting non-trial, trial and project level assignments within the team. The ability to ensure quality on-time fulfillment of deliverables is essential for this position.
Minimum Requirements:
" Three years of clinical research experience.
" Proficient use of Project Management tools such as MS Project.
" Prior project management experience creating project scope, timelines, cost management, quality management, communication plan, risk assessments and contingency planning.
" Previous experience leading cross-functional and cross-cultural teams or projects.
" Knowledge of regulations and guidelines that apply to conduct of clinical trials.
" Strong communication, leadership and networking skills.
" Strong self-management and organizational skills.
" Demonstrated problem solving abilities.
Apply:
For faster processing, please apply online and directly to the employer. Specific instructions on how to apply are available. (recommended)
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