Digital Marketing Manager
CONSAT
Shape Consat Telematics’ digital presence in public transportation and smart mobility. Create content, improve SEO and AI search visibility, and use campaign insights to guide performance.
Open
Parexel is a global clinical research organization serving biopharmaceutical companies throughout the development of new medicines. Its work spans Phase I–IV clinical trials, portfolio and trial management, regulatory strategy, market access, and lifecycle planning. With more than 21,000 professionals, Parexel combines clinical, regulatory, and therapeutic expertise with patient insights and innovative trial designs. The company supports research across areas including oncology, neuroscience, and rare diseases, with a focus on making clinical development more efficient and patient-centered.
Parexel Clinical Scientist FSP Remote United States
Support Parexel pharmaceutical clinical trials through data review, medical monitoring, and study operations. Help protocol leads and stakeholders deliver compliant clinical studies.
Description
- Support the CS Protocol Lead and study team in the clinical and scientific conduct of clinical studies
- Assist with adjudication, medical monitoring, imaging data reconciliation, meeting materials, and protocol deviation management
- Contribute to one or multiple clinical studies
- Lead limited-scope studies, such as Survival Follow-up
- Work with internal and external stakeholders, including study sites and committees, to advance clinical study objectives
- Complete all required training
- Submit accurate timesheets on schedule
- File expense reports when required
- Keep your CV current as required
- Maintain working knowledge of and follow Parexel processes, ICH-GCPs, and other applicable requirements
Requirements
- At least two years of pharmaceutical or clinical drug development experience within the past five years
- Therapeutic-area experience is required for Oncology IDV and GSM postings and preferred for other applicable postings
- Indication-specific experience is preferred
- Experience reviewing and resolving study data issues, including issued and resolved queries, medical record review, and identifying data errors requiring clarification with study sites
- Preferred experience reviewing patient data and resolving discrepancies related to adverse events, adverse-event trends, endpoint management, and laboratory results
- Strong oral and written communication skills
- Proficiency with Microsoft Office, including Outlook, Word, Excel, and PowerPoint
- OneNote experience is preferred
- Degree in life sciences
- Bachelor of Science, Bachelor of Arts, Master of Science, or PhD
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