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Associate Project Manager
hace 1 mes
The Associate Project Manager is a key member of our project management team, responsible for ensuring the successful delivery of clinical trials. This role involves working closely with the Project Manager and functional team members to track study budgets, project scope, and timelines in accordance with applicable standard operating procedures (SOPs), good clinical practices, regulatory, and study-specific requirements.
The ideal candidate will have excellent communication skills, be able to analyze discrepancies between planned and actual results, and participate in the development and implementation of corrective actions. They will also be responsible for ensuring that study-specific documents and project deliverables meet requirements.
We are looking for a motivated and organized individual who is knowledgeable about clinical research projects and is looking to continue learning. If you are a team player who is driven by science and innovation, and is looking for a challenging role that will help you grow professionally, then we encourage you to apply.
Key Responsibilities:
- Communicate project information to stakeholders, including the Sponsor, vendors, and internal team members.
- Track and manage established plans to ensure all deliverables and milestones are met.
- Coordinate tasks and deadlines between different departments involved in the project.
- Contribute to the management of needs and expectations of the Sponsor and other internal and external project stakeholders.
- Contribute to adequate training of team members on the project.
- Plan the activities and resources required for the project.
- Manage the quality of assigned work.
- Assist with providing project status updates.
- Analyze discrepancies between planned and actual results and participate in the development and implementation of corrective actions.
- Assist with enforcing effective change control and risk management throughout the project.
- Develop/review project operational plans and manuals as applicable.
- Assist with ensuring that study-specific documents and project deliverables meet requirements.
- Participate in the planning and conduct of Investigator's Meeting.
- Support the sites and ensure that each site has the necessary material to adequately perform the study.
Requirements:
- Knowledge of clinical research projects and good clinical practices.
- Excellent communication and analytical skills.
- Ability to work in a team environment and manage multiple tasks and deadlines.
- Strong organizational and problem-solving skills.
- Ability to adapt to changing priorities and requirements.
What We Offer:
- A stimulating work environment with a team of brilliant and driven colleagues.
- Attractive advancement opportunities.
- A competitive salary and benefits package.
