Design and manage the analytical strategy for a pegylated enzyme therapeutic program. Lead SEC-HPMC method development and validation for Phase 3 registration activities while providing SME guidance to the project team.
ProPharma
7 Remote Job Openings at ProPharma
Conduct 3 to 6 veterinary GCP audits for clinical studies involving animal patients. Ensure audits are performed against protocols, SOPs, local requirements, and VICH GL9 standards.
Lead the legal aspects of advertising and promotional review for drugs, biologics, and medical devices. Act as the lead for legal guidance and compliance during Promotional Review Committee (PRC) meetings.
Drive revenue growth by identifying new leads and maintaining long-term client relationships within the Clinical Research Solutions sector. Manage the full sales cycle from lead generation and proposal writing to contract negotiation and closing.
The Study Coordinator serves as the primary point of contact for site communications, managing document submissions and patient recruitment activities. They are responsible for data entry, monitoring clinical databases, and ensuring documentation complies with IRB/FDA policies.
French Speaking Medical Information Specialist - Graduate Opportunity
ProPharma
·
Full Time
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6 months ago
ProPharma
The role involves responding to medical and safety-related inquiries from healthcare professionals and patients, documenting adverse events, and providing accurate information based on approved resources. Additionally, the specialist will support service quality and contribute to process improvements.
French speaking Medical information Specialist- graduate opportunity
ProPharma
·
Full Time
·
9 months ago
ProPharma
The role involves responding to medical and safety-related inquiries from healthcare professionals and patients, using approved product information to provide accurate responses. Additionally, the specialist will document adverse events and support service quality through checks and training of new team members.
