What are the responsibilities and job description for the Clinical - Project Coordinator position at Aequor?
Job Description: Project Coordinator – MEG: Medical Evidence Generation
Position is 50% onsite
Job Description: Responsibilities:
Position is 50% onsite
Job Description: Responsibilities:
- Publications tracking and planning: Responsible for tracking congress and manuscript publications ensuring adherence to internal deadlines.
- Maintain internal planning Drive transparency of the medical evidence generation Medical Evidence Generation (MEG) congress disclosures.
- Project Management: this role will also play a pivotal role in supporting various project management needs across divergent functions
- Cross-functional Collaboration: Partner with cross-functional team members to execute the integrated congress disclosure planning.
- Compliance: Proficient in industry regulations and guidelines relevant to congresses.
- Timeline Management: Coordinate review and ongoing communication with cross-functional teams (Global Development, Worldwide Medical, Scientific Communications, Congress planning teams) to ensure adherence to timelines
- Stakeholder Communication: Maintain clear communication with key stakeholders, providing regular updates on progress and addressing concerns and changes.
- A minimum of a bachelor’s degree in life sciences, technical discipline, or allied business function
- Minimum of two year’s experience in the Pharmaceutical/Healthcare industry experience
- Strong project management skills, including the ability to manage multiple projects simultaneously
- Familiarity with document management systems such as Veeva platforms (Vault, CRM, CARA, PRISM) and other database platform experience.
- Excellent written and verbal communication skills
- Strong computer knowledge and skills including MS Office and Internet platforms
