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• Regularly engage with external clients in all tasks and responsibilities.
• Utilize expertise in technical, therapeutic areas, and company processes to create a thorough database design.
• Collaborate with internal departments to understand company capabilities and evaluate requests feasibility for meeting client requirements in study design.
• Provide consultancy to clients on study design options, highlighting risks and budget impacts in collaboration with the Global Study Manager (GSM).
• Enhance consultancy services at the study program level.
• Demonstrate exceptional interpersonal and communication skills to foster strong relationships internally and externally for top-notch study design.
• Manage internal processes and communications related to study design, ensuring seamless integration into the database and global monitoring plan.
• Conduct thorough self-reviews for quality assurance.
• Document and address all customer needs regarding study design.
• Operate effectively in a fast-paced environment with shifting timelines and priorities.
• Exhibit strong self-organization and priority management skills.
• Contribute to functional meetings, offering insights to keep processes current.
• Adhere to the internal Central Lab Global Project Management strategy.
• Oversee a portfolio of global and local studies of varying complexities.
• Foster a culture of continuous improvement, quality, and productivity.
• Preferred Bachelor’s degree in a life science field.
• Minimum of six (6) years of experience in Central Lab Project Management or similar industry roles.
• Strong skills in planning, organization, and problem-solving.
• Exceptional verbal and written communication abilities.
• Medical coverage
• Dental benefits
• Vision care
• Life insurance
• STD/LTD coverage
• 401(k) options
• Paid Time Off (PTO) or Flexible Time Off (FTO)
• Tuition reimbursement opportunities
• Employee Stock Purchase Plan
