Clinical Affairs Intern

We are seeking an experienced Senior Director or Vice President of Regulatory Affairs (DOE). As the head of Regulatory Affairs you will be responsible for leading and managing all aspects of Clinical and CMC Regulatory Affairs. The ideal candidate will have a strong background in cell therapy with experience in early development regulatory affairs (pre-IND...

MISSION Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases affecting children and adults. Propelled by our passion for patients and their families, we're focused on turning possibilities into realities. Using data and meaningful evidence, our goal is to transform scientific discoveries into therapies...

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...

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...

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...

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

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...

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...

Our Company:Evestra, Inc. is an emerging biopharmaceutical company that focuses on developing and commercializing women’s healthcare products. Based in San Antonio, Texas, Evestra’s mission is to improve the health and well-being of women around the world through innovative technologies and products. Responsibilities:Develop and oversee regulatory...

Our Company:Evestra, Inc. is an emerging biopharmaceutical company that focuses on developing and commercializing women’s healthcare products. Based in San Antonio, Texas, Evestra’s mission is to improve the health and well-being of women around the world through innovative technologies and products. Responsibilities:Develop and oversee regulatory...

Our Company:Evestra, Inc. is an emerging biopharmaceutical company that focuses on developing and commercializing women’s healthcare products. Based in San Antonio, Texas, Evestra’s mission is to improve the health and well-being of women around the world through innovative technologies and products. Responsibilities:Develop and oversee regulatory...

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 TITLE: Director/Senior Director, Medical Affairs DEPARTMENT: Clinical Development LOCATION: South San Francisco, California TYPE: Full-Time (Hybrid) Are you a medical affairs leader with late stage into commercialization experience in kidney and/or immune-mediated diseases? Join HI-Bio, Inc. a clinical-stage biotechnology company based in South San...

Senior Director / Director, Medical Affairs Clinical Development South San Francisco, Hybrid JOB TITLE: Senior Director/ Director, Medical Affairs DEPARTMENT: Clinical Development TYPE: Full-Time (Hybrid) Are you a medical affairs leader with late stage into commercialization experience in kidney and/or immune-mediated diseases? Join HI-Bio, Inc. a...

Job Title: Head of Regulatory Affairs - Biologics and DermatologyCompany Overview: Join a leading biopharmaceutical company at the forefront of innovation in biologics and dermatology. Our client is committed to developing transformative therapies that address unmet medical needs and improve the lives of patients globally. Their is dedicated to pushing the...

The Global Medical Affairs and Evidence Generation group delivers ambitious, patient-focused cross-regional and cross-indication medical strategies, driving data generation and dissemination, to maximize patient benefit from argenx products. The Global Medical Affairs Medical Director will provide expert medical leadership to guide development, launch...

Director of Regulatory Affairs San Jose, CA REF DESCRIPTION The position is independently responsible for development of global regulatory strategy and representation of Regulatory Affairs on R&D project teams. You will be responsible for managing all Regulatory Affairs activities (nonclinical and clinical) for investigational drug-device combination...

JOB TITLE: Director/Senior Director, Medical AffairsDEPARTMENT: Clinical DevelopmentLOCATION: South San Francisco, CaliforniaTYPE: Full-Time (Hybrid)Are you a medical affairs leader with late stage into commercialization experience in kidney and/or immune-mediated diseases? Join HI-Bio, Inc. a clinical-stage biotechnology company based in South San...