
Operations Project Coordinator
2 weeks ago
This role provides project support to a scientific writer, focusing on review and approval processes.
Key Responsibilities: Execute services and meet planned deliverables in line with defined roles and responsibilities.
Support the setup and maintenance of information in Datavision and other systems, including data updates, timelines, milestones, author agreements, and ethics committee authorizations.
Collaborate with the TA Scientific Lead to ensure accurate budget planning, tracking, and reporting.
Support the setup and maintenance of Veeva Vault: ensuring all key documents are present and approved as necessary.
Coordinate external service providers, including contract management and procurement.
Provide project management support to the Scientific Writer, ensuring effective end-to-end project delivery and approval through medical legal regulatory review.
Requirements Education: A bachelor's degree or higher in life sciences or an equivalent combination of education, training, and experience is required.
Experience: At least 7 years of operational experience in a pharmaceutical company, preferably with medical legal review or relevant industry experience.
Skills/Qualifications: Strong technical and organizational skills (Excel, Power Point).
Detail-oriented.
Benefits Our purpose is to reimagine medicine to improve and extend people's lives.
We value our associates' contributions and offer a range of benefits to support their well-being.
You'll receive comprehensive compensation and rewards packages that reflect your skills and qualifications.
Commitment to Diversity and Inclusion We strive to create an inclusive work environment that represents the patients and communities we serve.
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