Director, Clinical Development Hepatitis. Director, Clinical Development. You will typically lead or assist on multiple components of clinical trial programs in Hepatitis clinical development. You will help design, conduct, and evaluate Phase 1-4 clinical trials and provide expertise in clinical hep...
The Clinical Scientist will lead the scientific planning and collaborate with both Clinical Research, Pharmacovigilance and Clinical Operations in the execution of one or more clinical trials or significant aspects thereof. Proficient scientific expertise to propose, design, and execute clinical res...
Provide expert guidance on all aspects of clinical pharmacology programs supporting drug discovery and clinical development, including authoring clinical protocols, study reports, data analysis (exposure/efficacy/safety) to supporting development and registration of IDEAYA products. It has establish...
This involves working closely with Clinical Operations, Clinical Development, Clinical Supply Chain, Medical Affairs, Regulatory, Legal, and other teams across Alumis. Director is responsible to ensure quality is embedded throughout the lifecycle of all the ongoing clinical programs through oversigh...
The Medical Director is involved in the design, safety monitoring, and data analysis of the Company’s late-phase clinical trials in endocrinology. As such, the Medical Director is an important and visible member of the clinical development team. The Medical Director position is based in the United S...
Senior Scientific Director, Toxicology - San Diego, CA (Hybrid). Represent Preclinical development on discovery and development teams and regularly interfaces with internal and external colleagues to ensure timely and accurate dissemination of Safety Pharmacology and Toxicology findings. Evaluate, i...
Under the direction of the Executive Director, Clinical Operations, this role will support and manage several aspects of one or more AAV gene therapy clinical trials, including engagement and direct oversight of the clinical centers, investigators, study coordinators, and clinical CROs. Under the di...
Review clinical trial documentation for data integrity and compliance with Good Clinical Practice and regulations including key clinical and IND/NDA enabling documents. Clinical Quality Assurance contract- Director level. At least 5 years of experience in Clinical Quality Assurance or Clinical Opera...
One of our premier clients in the Bay Area is seeking to add a Associate Director Clinical Operations to their team!. Oversee the planning, execution, and closeout of clinical trials. Minimum of 5 years’ experience in clinical operations. Enthusiasm for learning and growing within the clinical resea...
Support, as the clinical representative, the transition of preclinical projects to clinical development. Our biotech client is seeking a highly motivated Medical Director with significant experience in clinical development to join our team developing novel and innovative engineered T cell-based ther...
They are seeking a highly skilled and experienced an Associate Director OR Director, Medical Writing to lead their Medical Writing team. Direct the planning, preparation, and finalization of a wide range of clinical and regulatory documents, including but not limited to Clinical Study Reports (CSRs)...
The Director of Clinical Quality Assurance (CQA) is a hands-on position responsible for ensuring clinical trials adhere to applicable GCP regulations (e. Review clinical trial documentation for data integrity and compliance with Good Clinical Practice and regulations including key clinical and IND/N...
Job Title: Senior Director of Clinical Quality Assurance. Meet is partnering with an Auto-Immune biotech to find them a Senior Director of Clinical Quality Assurance. This role demands proficiency in Good Clinical Practices (GCP) and Good Pharmacovigilance Practices (GVP), along with pertinent US an...
Senior Director, Clinical Data Management. The Head of Clinical Data Management (Senior/Executive Director) will report into the VP of Biometrics and be responsible for building the CDM department from scratch. With a rapidly advancing small molecule, clinical-stage pipeline, this company is looking...
Demonstrated understanding of regulations and guidelines governing clinical trial operations, including good clinical practice, clinical trial design and execution, the patient journey, clinical pharmacology, biostatistics, and clinical operations. Director, Clinical Operations w...
You may act as a Clinical Development Lead and Physician Responsible on clinical trial programs in the Inflammation and Fibrosis therapeutic area. As Clinical Development Lead, you will be accountable for the design, conduct, evaluation, close-out and reporting of clinical trials for the assigned mo...
Under the direction of the Executive Director, Clinical Operations, this role will support and manage several aspects of one or more AAV gene therapy clinical trials, including engagement and direct oversight of the clinical centers, investigators, study coordinators, and clinical CROs. Under the di...
You will typically lead multiple components of clinical trial programs in IBD/inflammation clinical development. Provides scientific and clinical guidance to cross-functional teams and colleagues to meet clinical development project deliverables and timelines. Provides input into, or otherwise leads...
The Director, Clinical Operations will lead and manage the assigned clinical operations team and have a key role in setting and executing departmental strategy. Oversees clinical trial agreements, budgets, expenditures and payments for clinical studies. Ensures the timely execution of clinical resea...
The Clinical Trial Capabilities (CTC) organization offers infrastructure, support, and solutions enabling the Clinical Operations and Development Organizations with rapid, efficient, and compliant clinical trial execution to deliver transformative medicines to patients. The Associate Director, will ...
Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management, regulatory agencies, and external peers. Leads teams within Clinical Pharmacology and Pharmacometrics and accountable for effective performance of the teams. Independently leads Clinical Pharmaco...
Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance. Pharmacovigilance / Clinical Development experience in the pharmaceutical industry. Effectively analyze and guide analysis of clinical data and epidemiological informa...
Medical Director, Clinical Development. Medical Director, Clinical Development. Medical Director who will be responsible for overseeing the direction, planning, execution, and interpretation of assigned clinical trials/programs and data collection. Manages program development, including working cros...
Our San Francisco Bay Area client is recruiting for a Director, Clinical Science to join their growing team. Advanced Clinical/Science Degree is preferred with 2 plus years of experience in Clinical Science. Provide scientific support for clinical development activities in collaboration with interna...
Director, Clinical Development. You will typically lead or assist on multiple components of clinical trial programs in Hepatitis clinical development. You will help design, conduct, and evaluate Phase 1-4 clinical trials and provide expertise in clinical hepatitis. Working in collaboration with the ...