Study Director Salary at Haligi Ng Bata Inc BETA

Smithers Environmental Risk Sciences division is seeking applicants for a full-time Senior Scientist opportunity at our Wareham, MA location. This position requires candidates to be currently authorized to work in the United States without sponsorship, or an immigration case, now or in the future. Candidates should have a Ph.D. or equivalent doctoral degree or possess an equivalent combination of graduate-level education and experience. The Senior Scientist is expected to have experience working with radiolabeled (mainly C-14) compounds and familiarity with various study designs and methodologies in Environmental Fate and Plant Metabolism. Responsibilities: Ensure all work complies with Good Laboratory Practices (GLP) regulatory requirements. Implement management directives quickly and efficiently. Review and sometimes write reports and provide training and mentorship to junior staff members. Serve as a study director within the Environmental Fate and Metabolism department. Direct and

Job Description Job Description We are hiring! The Medical Laboratory Scientist will engage in advanced sample processing, microbiology, equipment uses, maintenance, troubleshooting, submission of quality control data, and point tech duties, including data form creation and review. The Medical Laboratory Scientist will refine skills in the areas of attention to detail, problem-solving, and communication as they begin to mentor and train Medical Laboratory Technicians. This is an exempt role with no supervisory responsibility. Role Responsibilities Determine the acceptability of samples for testing according to established criteria. Advanced sample processing for blood, urine, cerebrospinal fluid, and other specimens in accordance with SOPs and/or Sponsor requirements. Monitor and operate instrumentation, including chemistry, hematology, coagulation, and urine analyzers. Notify vet staff of clinically significant results. Preventative maintenance and quality control of all analyzers Col

Smithers Environmental Risk Sciences division is seeking applicants for a full-time Chemist II opportunity at our Wareham, MA location. This position calls for proven expertise in the technical and experimental conduct of Environmental Fate and Metabolism studies. The Chemist II is expected to be proficient with standard and complex laboratory procedures, instrumentation and method development, and function as a lead in the implementation of solutions to common issues. The Chemist II is expected to and have significant experience with most types of study design/methodologies and have an excellent understanding of GLP requirements and their application for all Environmental Fate and Metabolism processes. Job Summary This position requires proven expertise in the technical and experimental conduct of Environmental Fate and Metabolism studies. The Chemist II is expected to be proficient with standard and complex laboratory procedures, instrumentation and method development, and function a

Your New Company! At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. About The Role Works under the guidance of designated Study Director(s), Contributing Scientists and Principal Investigators, as appropriate, to provide administrative and professional support for accurate

Clinical Veterinarian Job Description Summary The Clinical Veterinarian is responsible for examining, diagnosing, and treating laboratory animals to ensure their health and compliance with regulations governing humane and ethical treatment. This role supports study conduct through collaboration with Study Directors and other personnel. A key contributor to the reproductive toxicology department, particularly in infant care and dam assessments, the Clinical Veterinarian also develops staff training programs and care guidelines for high-risk animals. Hiring Requirements Time Type: Full-time (40 hours/week) Remote Type: On-site Compensation: 140,000-180,000 Depending on experience and certifications Primary Location: Sacramento, CA About the Role This site was initially focused as a CDC quarantine facility but has grown to a center of excellence for discovery phase biopharmaceutical studies focusing on NHPs for non-GLP general therapy, early discovery studies, and model development. The s

Clinical Veterinarian Job Description Summary The Clinical Veterinarian is responsible for examining, diagnosing, and treating laboratory animals to ensure their health and compliance with regulations governing humane and ethical treatment. This role supports study conduct through collaboration with Study Directors and other personnel. A key contributor to the reproductive toxicology department, particularly in infant care and dam assessments, the Clinical Veterinarian also develops staff training programs and care guidelines for high-risk animals. Hiring Requirements Time Type: Full-time (40 hours/week) Remote Type: On-site Compensation: 140,000-180,000 Depending on experience and certifications Primary Location: Sacramento, CA About the Role This site was initially focused as a CDC quarantine facility but has grown to a center of excellence for discovery phase biopharmaceutical studies focusing on NHPs for non-GLP general therapy, early discovery studies, and model development. The s

JOB SUMMARY: The Study Director/Scientist I is responsible for managing all phases of animal studies ensuring company strategies are implemented and company goals are achieved. PRIMARY RESPONSIBILITIES: •Provide expertise in areas of design, implementation and analysis of in vivo, in vitro, or toxicology studies •Responsible for reviewing pre-clinical data •Provide hands-on technical execution of studies if required •Provide study design and effective protocol development •Develop, approve, and distribute study-related documents and other study tools •Oversee study planning, initiation, and study-closure processes •Create metrics, complete data analysis, study reports and presentations •Act as key point of contact and facilitate communication across Crown Bioscience departments, providing relevant information •Act as key point of contact for Crown Bioscience customers by providing regular updates •Review adverse events for safety and effectiveness information •Track and report progress

JOB DESCRIPTION Function: The Regulatory Scientist II will be assigned as a Study Director, as defined by the U.S. FDA Good Laboratory Practice (GLP) regulations (21CFR58), and will serve as the single point of study control with overall responsibility for the scientific, technical and regulatory conduct of studies as well as for the interpretation, documentation and reporting of results. The Regulatory Scientist I / II works in conjunction with the Scientific Director for the Institutional Office of Regulated Nonclinical Studies (ORNcS), study sponsors and/or funding agencies to design and execute regulated nonclinical studies compliant with the U.S. FDA GLP regulations or under quality systems that utilize the US FDA GLP regulations as a reference standard. The Regulatory Scientist I / II may also function as a Principal Investigator for extramurally funded research programs and be expected to manage complex programs with multiple studies. ESSENTIAL JOB FUNCTIONS Responsible for the