Temporary and temp-to-hire clinical staffing solutions for the pharmaceutical and biotech industries.
Expert staffing & recruiting for life science operations, and unparalleled access to top professionals in Drug Safety, Regulatory Affairs, Clinical Operations, and Medical Writing.
Temporary, temp-to-hire and direct placement staffing services for the Pharmaceutical and Biotech Industries.
ClinCrowd supplies key contract or contract-to-hire resources for staff augmentation, or we can provide teams of consultants to help our clients complete their deliverables on time and with the highest level of quality. We take a consultative approach with our clients, tailoring our solutions to our clients’ needs.
Top talent for pharmaceutical and biotech programs.
Staffing & Recruiting Beyond the Bench
We understand that success in the life science industry relies on more than laboratory expertise. That’s why we cover a wide range of crucial functions beyond the research facility.
Whether you need skilled professionals to ensure regulatory compliance, manage clinical data, produce high-quality medical documentation, or drive strategic medical affairs initiatives, we have the expertise to fulfill your staffing needs.
Talent Staffing and Placement Expertise
Drug Safety, Pharmacovigilance & Risk Management
High-quality talent in the areas of Drug Safety/Pharmacovigilance and Risk Management to assist clients with case processing, vendor management, risk management plans, signal detection activities, responses to questions from health authorities, safety sections of submissions, such as NDAs, and aggregate reports, like PBRERs and DSURs.
ClinCrowd can also assist Regulatory Affairs departments with Regulatory Strategy, Labeling initiatives, Regulatory CMC, Ad/Promo, Regulatory Medical Writing and Regulatory Operations. Our consultants can provide regulatory guidance for submissions to the FDA, EU and ROW.
Clinical Trial Operations
Providing Clinical Project Leads/Project Managers, Senior Clinical Trial Managers, and in-house CRAs and CTAs. Our Clinical Operations consultants can assist our clients with Phase 1-Phase IV clinical trials, including site selection, budgeting, protocol development, monitoring, managing vendors, tracking of KPIs and TMF maintenance.
ClinCrowd can provide talent within the areas of Medical Affairs/Medical Information, Quality Assurance, Validation and Compliance, GXP Auditing, and Clinical Data Management and Biometrics.