Job Listings

Actively searching for an experienced AD/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.

Extensive Knowledge of FDA regulations and their practical implementation Manage and track the preparation and return of investigational supplies at individual sites RN or Bachelor and/or advanced degree in biological sciences or related field Paying up to high $130’s

Provide statistical input for protocol development, study design, and CRF development by actively contributing to study design considerations in internal and client meetings, and providing and discussing sample size scenarios.

Develop and execute regulatory strategy for the development of company programs, aligned with departmental objectives, timeframes and company goals.

Maddison Harry Life Sciences is seeking a highly experienced and dynamic individual to join our team as the Head of Global Quality. This senior leadership role will be pivotal in ensuring the highest standards of quality are maintained across our pharmaceutical and biotech operations worldwide. The ideal candidate will possess a deep understanding of global […]

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.

The candidate specializing in High-Throughput Screening (HTS) will lead the development and execution of screening strategies to identify and validate new drug candidates.

The VP, Business Development would implement full business development cycle and create, build, and expand strategic partnerships.

The VP, Product would help develop, launch, and grow products that addresses a need for their target clients.

The Sr. Scientist of Stem Cell Biology would be responsible for designing, executing, and analyzing preclinical experiments.

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.

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.

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.

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.

Provide SAS statistical programming support for multiple clinical research projects or regulatory submissions.

Work with a leader of the Statistical Operations management team to manage clinical trial programs/projects from one or multiple clients.

Working as leading statistician on multiple studies/projects across different therapeutic areas.

Lead projects with higher level of complexity/challenges/difficulties, and lead efforts to resolve complex statistical programming issues or problems.

Lead complex/large-scale clinical trial in early Phase clinical development within a program.

Provide Statistical Input into clinical development plans, study reports, regulatory documents and publications ensuring accurate deliverables.