Anne Roc

Medical Education Grants Manager

‍Takeda

Medical Education Grants Manager

‍Takeda

#Medicaleducation #Medicalwriting

#Northamerica

Detail-oriented, adaptable director-level professional experienced in blending analytic, scientific, and strategic information to identify and pursue business opportunities in a rapidly changing healt

Debra Webster

Vice President, Regulatory Affairs and Medical Writing

‍BlueRock Therapeutics

Vice President, Regulatory Affairs and Medical Writing

‍BlueRock Therapeutics

#clinicaldevelopment #regulatoryaffairs #medicalwriting

#NorthAmerica

Debra Webster is based out of Leawood, Kansas, United States and works at Bluerock Therapeutics as Vice President, Regulatory Affairs and Medical Writing.

Eleni Allen

Director, REMS Strategy and Execution, US Medical Affairs

‍GSK

Director, REMS Strategy and Execution, US Medical Affairs

‍GSK

#MedicalWriting #Pharmaceutical #ClinicalDevelopment

#NorthAmerica

Eleni Samaras Allen, Director, REMS Strategy and Execution at GSK oversees REMS program development, execution, and strategy.

Laura Troast

Director, Clinical Data Disclosure & Transparency

‍Merck

Director, Clinical Data Disclosure & Transparency

‍Merck

#MedicalWriting #ClinicalTrials #ClinicalDevelopment

#NorthAmerica

Laura Troast has been working in the disclosure and transparency space at Merck & Co., Inc. since 2006. She is a director within their Clinical Data Disclosure & Transparency (CDD&T) group, currently

Sameer Sharma

Associate Director, Clinical Trial Transparency

‍Merck Group

Associate Director, Clinical Trial Transparency

‍Merck Group

#Pharmacovigilance #MedicalWriting #ClinicalTrials

#Europe

Life science professional with 9 years of experience in Clinical Trial Transparency, Medical Writing, Medical Information, and Pharmacovigilance.