... Medpace, p reparing and reviewing regulatory documents and providing strategic regulatory advice to support clinical trial ... independently interact with national regional regulatory agencies. Medpace Overview Medpace is ...
... with the approved protocol, regulatory requirements, and applicable SOPs. Assist ... teams, including clinical operations, regulatory affairs, and data management. Provide mentoring ... GCP, ICH guidelines, and regulatory requirements related to clinical trials. ...
... with various functions such as regulatory affairs, product management, IT, and packaging development. The Label specialist supports the maintenance of process ...
... Clinical Operations Specialist Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and ... regulatory documents and updates for investigator ...
... support activities across both Medical Affairs and Clinical Development objectives for ... drug Attend and provide Medical Affairs support at scientific conferences Support ... across clinical and medical affairs globally Remote Engagement - Alternative channels ...
... a team of therapeutic and regulatory experts; Defined CRA promotion and ... disciplined approach. We leverage local regulatory and therapeutic expertise across all ...
... Role: In the Customer Support Specialist (Product Specialist) role, you will be the ...
... translate unique clinical, medical affairs and commercial insights into outcomes ... patient safety, protocol GCP regulatory compliance and data integrity. • Oversees ... Guidelines and other applicable regulatory requirements • Must demonstrate good computer ...
... . We translate unique clinical, medical affairs and commercial insights into outcomes ... on-site or remotely) ensuring regulatory, ICH-GCP and or Good ... ICH Guidelines and other applicable regulatory requirements • Must demonstrate good computer ...
... SOPs, GCP and applicable regulatory requirements; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and ... approach. We leverage local regulatory and therapeutic expertise across all ...