Clinical Project Manager - III
Yesterday
Description
• Act as a liaison with sponsor to oversee clinical studies to include: • Ensure study remains within scope and out of scope activities are identified and handled as appropriate • Perform risk management and contingency planning activities to ensure that all potential study risks, such as delays in study milestones and increased study costs, are managed in a proactive and efficient manner • Facilitate team coordination and work flow for projects • Develop and Monitor project timelines and resources allocated • Communicate up-to-date information regarding project progress to all relevant interested parties • Provide strategic input on enrollment and contingency planning • Vendor management to include procurement and negotiation of contracts • Lead project team meetings to ensure on-time deliverables • Assist in protocol development and CRF design • Track departmental carbon footprint and implement policies, procedures, and practices to decrease negative impact on the environment • Ensure all departmental purchases and practices reflect the company’s corporate citizenship policy • May manage clinical study budget and contracts
Requirements
• Knowledge of FDA and International Conference of Harmonization and Good Clinical Practices (ICH/GCP) Guidelines • Excellent written and verbal communication skills and detail-oriented skills • Various computer skills – Excel, Word, PowerPoint, Microsoft Outlook • Extensive understanding of principles, concepts, practices, and standards of clinical research • Excellent leadership skills • Excellent organizational skills, including the ability to handle multiple assignments • Possess full working knowledge of all required clinical study tasks and elements from study initiation through completion • Ability to ensure a good customer relationship is established and maintained
Apply NowSimilar Jobs
2 days ago
Research Assistant role focusing on suicide prevention and PTSD project management at Ohio State University.
4 days ago
As Clinical Trial Manager II at CPC, manage site operations and ensure adherence to clinical trial regulations.
🇺🇸 United States – Remote
💵 $72k - $88k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🗽 H1B Visa Sponsor
December 3
Oversee planning and execution of clinical studies at Penumbra. Ensure data safety and effectiveness while collaborating with various stakeholders.
November 30
Assist investigators with clinical data management and statistical analysis at Centene.
November 28
Oversee clinical research activities for SI-BONE's sacropelvic device studies. Ensure compliance and support the clinical team effectively.