Review and approve project invoices on behalf of Project Leader or Project Integration Manager.
Implement change order control processes.
Ensure Project Leader has timely and accurate data on areas including cost, schedule, scope, utilization, change orders, quality to support better decision-making.
Develop and maintain relevant sections of Project Execution Plans.
Assist project sub-team leads in defining resource requirements, utilizes systems in order to monitor status.
Prepare correspondence, including meeting minutes, for study team and / or customer.
Organize and support Project Leader in managing internal study team and customer meetings.
Prepare presentation materials including study data for internal study team and customer meetings.
Support study file review and audits as needed.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
Strong written and verbal communication skills including good command of English language.
Results-oriented approach to work delivery and output.
Problem solving skills
Planning, time management and prioritization skills.
Ability to handle conflicting priorities.
Attention to detail and accuracy in work.
Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.
Ability to influence without authority.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor's degree in life sciences or other related field and minimum of 1 year of relevant clinical research experience or project management activities (with analytical / financial skills - preferably);
Excellent english command
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