5+ yrs of exp in healthcare content mgmt, scientific communications, or project mgmt, preferably within a digital health platform, medical communications agency, or pharmaceutical environmentRequired Candidate profileUndersta...

QC and formatting of clinical trial protocols, informed consent forms (ICFs), clinical study reports (CSRs), investigator’s brochures (IBs), and clinical data summaries for phase 1-phase 3 and post-marketing surveillance stu...

As a medical writer, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our organization. You will cover topics in clinical trials, treatments, procedures, medical devices, p...

As a medical writer, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our organization. You will cover topics in clinical trials, treatments, procedures, med Responsibilit...

Job Title 1 : Salesforce Marketing Cloud Developer / ConsultantRole & responsibilitiesDevelop and implement campaigns using Salesforce Marketing Cloud toolsCustomize emails and landing pages using AMPscript and HTML/CSSIn...

JOB SUMMARYClinical Trial Disclosure plays a critically important role in executing projects for Syneos global clients. He/she works as part of high-performing teams on challenging assignments involving the processing of comp...

OverviewWe have an exciting role of Medical Writer to drive and translate creative and contemporary ideas to solid design and impact. You will have a key role in design and deployment of creative campaigns with our global cl...

 Regulatory medical writers play a significant role in preparing documents and ensuring that they are accurate, concise, and compliant with the prevalent standards. Summarizing safety and/or efficacy data for a CSR R...