This is a fully remote position, open to applicants in United States.

📋 Description

• Plan, coordinate, and manage all phases of clinical trials, which encompass project planning, budgeting, resource allocation, execution, and closure.

• Ensure compliance of clinical trials with established protocols, standard operating procedures (SOPs), Good Clinical Practice (GCP), and relevant regulatory requirements.

• Act as the main point of contact for sponsors, investigators, and stakeholders.

• Deliver timely and precise updates regarding project progress.

• Identify potential project risks and create, as well as implement, strategies for mitigation.

• Collaborate with both internal teams and external vendors to achieve project objectives.

• Supervise data management tasks and guarantee the accuracy and integrity of clinical trial data.

• Conduct regular project meetings, documenting and following up on actions and decisions.

• Prepare and present project reports to senior management and stakeholders.

• Complete all required training promptly and in accordance with company policies.

⛳️ Requirements

• Bachelor’s degree in a life science or a related field.

• A Master’s degree or relevant certification is preferred.

• At least 5 years of experience in clinical project management within a Contract Research Organization (CRO), biotechnology, or pharmaceutical company.

• Comprehensive knowledge of clinical trials, encompassing their planning, execution, and regulatory considerations.

• Strong project management capabilities, with the ability to handle multiple projects at once.

• Exceptional communication and interpersonal skills.

• Strong analytical and problem-solving abilities, along with the flexibility to adapt to changing conditions.

• Proficient in project management software and other pertinent tools.

• Must possess authorization to work in the United States; employer is a participant in E-Verify.