Clinical Affairs Manager

Job DescriptionJob DescriptionPosition Summary: Responsible for planning, executing, and managing the global Clinical Affairs activities including initiating and monitoring clinical trials, developing, overseeing and monitoring post-marketing studies and supporting pre-clinical studies as necessary.Position essential duties and responsibilities: Include the...

In order to move forward, you will need to create an account. Your password must be eight characters long, contain at least one special character, one capital letter and a number. We look forward to discovering your talents. Executive Director, Clinical and Medical Affairs Welcome to an inspired career. At Halozyme, we are reinventing the patient...

Essential Duties and Responsibilities This is a full-time San Diego office-based position. The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. Participates in corporate development of methods, techniques and evaluation criteria for projects,...

Essential Duties and Responsibilities This is a full-time San Diego office-based position. The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. * Participates in corporate development of methods, techniques and evaluation criteria for projects,...

Bayside Solutions is seeking a Director, Clinical Affairs IV to be part of our client' s team in South San Francisco. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s Clinical, Clinic, Director, Development, Pharmaceutical, Client, Healthcare, Staffing

Location: San Jose, CA About: Currently working with a medical device company dedicated to developing and commercializing breakthrough catheter devices that revolutionize patient care on a Regulatory Head position. In this critical role, you will play a pivotal role in ensuring our breakthrough catheter devices navigate the regulatory pathway efficiently...

Responsibilities and Duties:Responsible for timely planning, coordination, and execution of regulatory submissions to FDA and other jurisdictionsOversee the authoring, review, approval and submission of Clinical, Nonclinical, and CMC documents for regulatory submissionsConduct regulatory review of submission documentsCoordinate with external publishing...

Job DescriptionJob DescriptionUnder the direction of the Director of Patient Care Services, the Clinical Manager monitors/assures, supervisesand directs field staff & clinical office staff activities; is responsible for field staff competencies, and their safe and efficient comprehensive end of life care delivery to patients. The manager supervises a variety...

Essential Duties and ResponsibilitiesThis is a full-time San Diego office-based position. The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.  Participates in corporate development of methods, techniques and evaluation criteria for projects,...

Job Details Job Location SLO Office - San Luis Obispo, CA Position Type Full Time Travel Percentage None Job Category Medical Management Description Salary Range: $22.56 - $31.58 per hour Job Summary A Clinical Support Associate Enhanced Care Management (CSA-ECM) is assigned to Enhanced Care Management Unit of Medical Management. The CSA-ECM reports to the...

Overview: My client is a successful, midsize biotech that continues to explore the potential of cortisol modulation across various disease areas, including endocrinology, oncology, metabolism, and neurology. They are looking to bring no a Sr. Manager of Regulatory Affairs to play a part in their early and late stage clinical trials. Responsibilities: Provide...

Job SummaryThe Living Therapeutics Initiative seeks a highly motivated Regulatory Affairs Senior Manager to manage the regulatory affairs, author and assemble IND applications, and help manage FIH studies advancing UCSF-developed cellular therapy candidates. The successful candidate will work in a dynamic academic environment, working across various...

Description Southwest Strategies and Katz & Associates (Katz) are seeking a full-time Manager of Public Affairs to direct and support project teams and deliver strategic communications for clients in San Diego and throughout the state of California. We are a full-service public affairs and strategic communications firm, focused on community and digital...

Company Location: Bay Area Comp: 150K-220K Position Reports to: VP of Regulatory and Quality Director of Regulatory Affairs -San Francisco We are seeking a highly motivated and experienced Senior Director of Regulatory Affairs for a Medical Device Orthopedic Portfolio. This person will lead interactions with regulatory agencies globally and help develop &...

Vir Biotechnology, Inc. is an immunology company focused on powering the immune system to transform lives by treating and preventing infectious diseases and other serious conditions, including viral-associated diseases. Vir has assembled two technology platforms that are designed to modulate the immune system by exploiting critical observations of natural...

Job DescriptionJob DescriptionSalary: $90KPurpose:The Regulatory Affairs Manager is responsible for managing the regulatory affairs department and functions to ensure regulatory compliance of quality management system.Duties & Responsibilities: Review and approve audit agenda, plan, summary reports for internal audits. Facilitate and participate in external...

Vir Biotechnology, Inc. is an immunology company focused on powering the immune system to transform lives by treating and preventing infectious diseases and other serious conditions, including viral-associated diseases. Vir has assembled two technology platforms that are designed to modulate the immune system by exploiting critical observations of natural...

Position: Medical Affairs Director Location: Foster City, CA, 94404 Duration: 8 Months Job Type: Contract Work Type: Remote Pay Rate: $75-$80/hr Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and...

The analyst works independently, under the direction of the Regulatory Affairs Manager, to review cooperative and industry-sponsored protocols, revise local informed consents (ICFs), and submit review packets (protocols, ICFs, and other required documents) to the UCSF IRB and external IRBs.- Day to day tasks include: - Assist Regulatory Affairs Manager with...

JOB TITLE: Director/Senior Director, Medical AffairsDEPARTMENT: Clinical DevelopmentLOCATION: South San Francisco, CaliforniaTYPE: Full-Time (Hybrid) Is this your next job Read the full description below to find out, and do not hesitate to make an application. Are you a medical affairs leader with late stage into commercialization experience in kidney and/or...