Job Listings

Current Job Openings

Executive Director of Regulatory Affairs
Actively searching for an experienced Executive Director of Regulatory Affairs to work onsite for an opportunity paying up to $250,000 with a 15% bonus, based on experience. This role involves developing and implementing regulatory strategies aligned with the company’s objectives and regulatory guidelines.
Director of Quality Assurance
We are actively searching for an experienced Director of Quality Assurance to work onsite for an opportunity paying up to $150,000, plus bonus, based on experience.
Principal Scientist
The candidate specializing in High-Throughput Screening (HTS) will lead the development and execution of screening strategies to identify and validate new drug candidates.
VP, Business Development
The VP, Business Development would implement full business development cycle and create, build, and expand strategic partnerships.
VP, Product
The VP, Product would help develop, launch, and grow products that addresses a need for their target clients.
Sr. Scientist, Stem Cell Biology
The Sr. Scientist of Stem Cell Biology would be responsible for designing, executing, and analyzing preclinical experiments.
Director, Business Development
The Director, Business Development is responsible for sourcing new client and project bid opportunities, and working with our proposals team to delivered tailored budgets and proposals to drive new project wins and meet our client’s business needs.
Sr./Clinical Research Associate
CRAs primary responsibility is to build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of clinical trials.
Senior Director, Regulatory Affairs
Reporting to the Chief Medical Officer, the Senior Director of Regulatory Affairs will be responsible for the development and execution of regulatory strategy and operations. This person will lead the development of all relevant regulatory documentation and registration strategies for both the EU and US.
Director, Clinical Operations
The Director will report to the VP, Clinical Operations and will work closely with a cross-functional team in a fast-paced high growth environment team to ensure that clinical trials are conducted on time and budget, and in accordance with applicable GCP/ICH guidelines and other regulatory requirements.
Statistical Analyst
Provide SAS statistical programming support for multiple clinical research projects or regulatory submissions.
Principal Biostatistician
Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or multiple clients.
Associate Director, Biostatistics
Working as leading statistician on multiple studies/projects across different therapeutic areas.
Principal Statistical Programmer
Lead projects with higher level of complexity/challenges/difficulties, and lead efforts to resolve complex statistical programming issues or problems.
Associate Director, Clinical Trials
Lead complex/large-scale clinical trial in early Phase clinical development within a program.
Associate Director, Biostatistics
Provide Statistical Input into clinical development plans, study reports, regulatory documents and publications ensuring accurate deliverables.