Project Coordinator MEG: Medical Evidence Generation - Artech LLC
Lawrence Township (50% onsite), NJ 08648
About the Job
Job Summary
Job Title: Project Coordinator – MEG: Medical Evidence Generation
Location: Lawrence Township, NJ (50% onsite)
Duration:06+ Months (Potential extension)
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.
Minimum Qualifications:
• 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
Job Title: Project Coordinator – MEG: Medical Evidence Generation
Location: Lawrence Township, NJ (50% onsite)
Duration:06+ Months (Potential extension)
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.
Minimum Qualifications:
• 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
Source : Artech LLC
