JOB TITLE : CLINICAL PHARMACOLOGIST, PHARMACEUTICALS
LOCATION: HOBOKEN
Our client, a biopharma industry leader, is focused on finding solutions for serious unmet medical needs. They are looking for a dedicated Clinical Pharmacologist to perform clinical data modeling simulation analysis to support their Clinical Pharmacokinetics team.
JOB TITLE: POST-MARKET CONSULTANT
LOCATION: MAPLEWOOD, MN
We have an excellent job opportunity available as a PSUR Writer. Duration: 6 months Our client is looking for this consultant to: Provides leadership and direction to the PMS staff. Conducts performance evaluations and makes recommendations in support of performance ratings, salary adjustments, promotions, etc. Facilities effective training and development opportunities
JOB TITLE: PROCESS VALIDATION ENGINEER
LOCATION: CAMBRIDGE, MA
We have an excellent opportunity available as a Process Validation Engineer. Duration: 6-12 months Our client is looking for this consultant to: Develop process validation protocols and other documentation for cell banking, cell culture and purification processes
JOB TITLE: CQV/EQUIPMENT VALIDATION
LOCATION: LOS ANGELES, CA
We have an excellent job opportunity available as a CQV/Equipment Validation. Duration: 6 months Our client is looking for this consultant to: Draft, write and execute protocols Write validation plans for equipment’s
JOB TITLE: TOXICOLOGIST
LOCATION: ROCHESTER, NY
Our global Med Device Client is seeking a Sr. Consultant to support the non-clinical safety division. This individual will support the research and development of new ophthalmic products as well as maintenance of business activities through design of programs and/or safety strategies, execution of toxicology studies designed to meet regulatory guidelines
JOB TITLE: REGULATORY SUBMISSION CONSULTANT
LOCATION: SANTA CLARA,CA
We have an excellent job opportunity available as a Regulatory Submission Consultant. Contract Length: 12 months Our client is looking for this consultant to: STED writing, reviewing and working cross functionally with multiple teams to update reviews. They have a STED template to work from. EU MDR submission work for Europe only
