: Our client is a leader in the chemicals, paints and coatings industry that has been in business for over 100 years. Their broad portfolio of material solutions helps advance their customers in many industry spaces like automotive, electronics, medical and food & beverage. While their Headquarters are based in Dallas, the company has over 7,500 employees working to serve their customer based worldwide from Amsterdam
GLP QA MANAGER, SR MANAGER- CONTRACT RESEARCH - FULL TIME Position Title: Quality Assurance Manager/Senior Quality Assurance Manager Department: Quality Assurance Summary: This position is responsible for overseeing the internal and external quality assurance audit program to ensure regulatory compliance for a preclinical contract research organization. This role requires the ability to work closely and effective
MEDICAL DEVICE STUDY DIRECTOR/ PRINCIPAL SCIENTIST SAN DIEGO, CA Medical Device Study Director/ Principal Scientist The Principal Scientist would participate in Medical Device & Therapeutic studies in the functional role of a Study Director to conduct and oversee pre-clinical studies (acute and chronic, GLP and non-GLP, rodents, rabbits, pigs, sheep) that evaluate implantable devices (blood glucose monitors, prosth
Medical Director for High Profile Pharmaceutical company Looking for an M.D. to work with the Head of Clinical Affairs with Oncology early and late phase VP would consider an individual from academia - provided they had a strong background in immunology/oncology/hematology or a seasoned Pharmaceutical Professional Director or Senior Director, Clinical Oncology Job Summary: Oversees one or more trials of medium to hi
Position Summary: The Clinical Researcht Manager is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). This one is a Global Phase 1b pivotal study. Reports directly to the Executive Director, Clinical (who reports to CMO). In concert with the ED, is accountable for achieving successful delivery of Company clinical team activities at the project level by meeting co
My client is expanding and looking to hire a Translational Scientist. The ideal candidate can come from a small molecule or biologics background, and this person will take on the following tasks: * Act as the primary point of contact for PK/PD related activities on preclinical and early clinical programs * Assess PK/PD data and incorporate endpoints for assessing pharmacodynamics, biodistribution and immunogenicit
My client is expanding and seeking a Scientist for a high impact role -- the ideal candidate will take on the following tasks: * Work closely with CROs and serve as study monitor for the design, conduct and reporting of pharm and tox studies * Write and review study protocols for collaborators and CROs * Prepare Preclinical Development SOPs and guidelines and finalize study reports * Write and review nonclinic
My client is expanding and looking to hire a Manager to direct a significant collaboration and oversee operational and scientific tasks. The ideal candidate will take on the following tasks: * Manage and monitor scientific protocols and project deliverables * Offer guidance and hands-on assistance on new test development * Prepare study reports and presentation materials as needed * Partner with management to
Our client is a world leader in laboratory instrumentation and services and has an opportunity for a Technical Sales Representative (TSR) for its industry leading analytical instrumentation used in R&D laboratories. The Technical Sales Representative will be responsible for direct sales of mechanical surface characterization instrumentation and services to customers covering TX, LA, AR and OK with an ideal base in Ho
Toxicologist / Principal Scientist Extractables & Leachables Medical Device Summary: Seeking Subject Matter Expert (SME) for a Senior Scientific role with biocompatibility and toxicology expertise in Extractables & Leachables for global medical device company. The right person my be able to work remotely, apply if you are interested and qualified. Responsibilities : Senior-level individual contributor responsible
