Project Manager

Job DescriptionJob DescriptionBenefits:

• 401(k)
• 401(k) matching
• Bonus based on performance
• Dental insurance
• Health insurance
• Vision insurance
• Wellness resources

Company Overview:


Crystal Bio Solutions, a member of Crystal Pharmatech, is a leading bioanalytical and biologics CMC analytical organization with operations in the San Francisco Bay Area and New Jersey. We specialize in GLP-compliant bioanalytical and biomarker services, as well as CMC analytical support for biologics, serving biotech and pharmaceutical clients from early discovery through clinical development. We are seeking a full-time Project Manager to support our Bioanalytical and Biomarker Services at our Pleasanton, California site.

Key Responsibilities:

• Provide oversight on the study throughout its life at CBS, including method development, method validation, sample/data analysis, and reporting.
• Work closely with lab staff, data analyst, technical writing, QC, QA, Procurement and Finance to ensure studies are completed and compensated on schedule.
• Maintain all communication with clients providing daily updates on all active projects while being vigilant for opportunities to earn additional business.
• Work with the client to resolve sample/data discrepancies.
• Monitor the progress of all assigned studies and alert management if work falls behind schedule.
• Provide project trackers for client communications and lead regular teleconferences to discuss study progress.
• Create project parameters and budget expectations and conduct periodic scope, schedule, and cost reviews using industry best practices, to identify needed adjustments
• Coordinate client visits and where needed.

Qualifications and Educational Requirements:

• Master's or bachelor's degree in biology, immunology, chemistry, pharmacology, or related scientific fields required.
• Minimum of 3 years' PM-related experience. Supervisory experience in both project and people management are desirable.
• Understanding of Ligand binding assays, LC-MS/MS, Cell-based assays, Immunogenicity assays, PCR and/or Flow cytometry assays is a plus.
• Familiar with requirements of FDA/EMA, GLP/GCLP regulations, and ICH guidelines.
• Multi-tasking capability to efficiently manage multiple projects simultaneously.
• Ability to achieve objectives/timelines through collaborative efforts with coworkers, managers, and clients.
• Good communication skills in both written and verbal and interpersonal skills are essential

Skills

• Proficient in MS Office, PM tools (e.g., Smartsheet, MS Project, etc.)

Location:
Pleasanton, California (On-site, 5 days on site)

Compensation:
Compensation will be based on experience and qualifications