Job Search | The Leading Life Science Recruitment Agency

• Philadelphia, Pennsylvania
• Negotiable
• Posted about 4 hours ago

Do you have a passion for the research and development of new Oncology Products? Would you like to be a part of an Organization that has had a generational impact on the Pharmaceutical industry? A top 10 Global Pharmaceutical company is looking to add a Director of Biostatistics to their oncolog...

• München (81249), Bayern
• £55000 - £85000 per annum
• Posted about 4 hours ago

An exciting Pharmaceutical company is currently seeking to hire a Clinical QA Manager to join their growing team in Munich. This position will provide comprehensive support clinical quality assurance (GCP), as well as perform occasional GCP audits. Key responsibilities of the Clinical QA Man...

• Munich, Bayern
• Negotiable
• Posted about 4 hours ago

A leading Pharmaceutical company is currently seeking to hire a Content & Project Manager to join their growing team in Munich. This position will be responsible for the design and implementation of a global electronic quality management system. Key responsibilities of the Content & Project ...

• Philadelphia, Pennsylvania
• Negotiable
• Posted about 5 hours ago

Do you have a passion for the research and development of new Oncology Products? Would you like to be a part of an Organization that has had a generational impact on the Pharmaceutical industry? A top 10 Global Pharmaceutical company is looking to add a Director of Biostatistics to their oncolog...

• California, USA
• Negotiable
• Posted about 19 hours ago

The clinical trial manager will be responsible for overseeing all aspects of assigned clinical trials. Vendor/CRO Oversight such as IVRS, central lab, etc. Review site study documents organize and manage internal team meetings, investigator meetings, etc. CRF/Study Planning

• South San Francisco, California
• Negotiable
• Posted about 19 hours ago

Company Summary: A well-established Biotechnology firm is currently seeking a driven and organized Quality Specialist with a strong background in Quality Management Systems and pharmaceutical development. You will play a key role in their quality management, drug safety and compliance. In addi...

• California, USA
• Negotiable
• Posted about 19 hours ago

The Clinical AD/Director will be responsible for overseeing the entire clinical trial. They will have strong experience implementing and monitoring clinical studies preferably in the diagnostics space. They will have lots of people management experience. Experience building/leading clinical...

• Bergenfield, New Jersey
• Negotiable
• Posted about 19 hours ago

Title: Senior Clinical Operations Manager Summary: A well-established global Oncology biotech company in New Jersey/Greater New York City area is seeking a Senior Clinical Operations Manager to help oversee clinical trial deliverables including timelines, budgets, and resource requirements ...

• Rockville, Maryland
• Negotiable
• Posted about 20 hours ago

Title: Clinical Project Manager Summary: A fast-growing pre-IPO CAR-T Immuno-oncology biotech company in Maryland is seeking a Clinical Project Manager to help oversee clinical trial deliverables including timelines, budgets, and resource requirements on their early phase clinical programs....

• Maryland, USA
• Negotiable
• Posted about 20 hours ago

Title: Clinical Project Manager Summary: A fast-growing pre-IPO CAR-T Immuno-oncology biotech company in Maryland is seeking a Clinical Project Manager to help oversee clinical trial deliverables including timelines, budgets, and resource requirements on their early phase clinical programs....

• Menlo Park, California
• Negotiable
• Posted about 21 hours ago

Title: Regulatory Publishing Manager Company Summary A small immuno-oncology biopharma company, in Menlo Park, is looking to bring on a Regulatory Publishing Manager to join their team, on a contract-to-hire basis. You will play a key role in publishing, submitting and maintaining regulatory fi...

• South San Francisco, California
• Negotiable
• Posted about 21 hours ago

Title: Global Studies Manager Job type: Contract Contract length: 1-3 year(s) Job responsibilities: Develop monitoring strategies, budgets and site selection. Provide clinical operations expertise to ensure operational feasibility and delivery Oversees forecasting of clinical/non-clinic...

• New York, USA
• Negotiable
• Posted about 21 hours ago

Creating or reviewing regulatory documentation for IRB submissions Overseeing all new submissions and continuing to review activities to ensure compliance Aiding in the preparation of responses to regulatory matters from regulatory authorities Supporting the clinical operations team

• Ohio, USA
• Negotiable
• Posted about 22 hours ago

Preparing and filing of new product labelling in adherence to regulatory and manufacturing standards Review and approval of Ad/Promo materials Preparing OPDP Submissions Ensuring that all regulatory labeling is completed on time and in compliance with the FDA and/or any other regulatory requ...

• Boston, Massachusetts
• Negotiable
• Posted about 22 hours ago

Assist in the preparation and submission of IND's, IMPD's, NDA's and other regulatory submissions Prepare and maintain regulatory submission trackers and notifications Manage the preparation and submission of Advertising and Promotion 2253/ Presubmission filings in coordination with team memb...

• San Diego, California
• US$80000 - US$125000 per year
• Posted about 23 hours ago

The candidate is responsible for creating and qualifying/validating analytical methods and providing technical guidance for development projects and commercial product creation. This role is responsible for starting, leading and delivering scientific research, while keeping a broad knowledge of ...

• New York, USA
• US$80000 - US$110001 per year
• Posted 1 day ago

A highly progressive Medical Communications agency is searching for a Senior Medical Writer to join their Scientific Services team. As the agency continues to grow, you will play a pivotal role in the content creation but also will have a hand in client relationships as well. You will be able to...

• Netherlands
• Negotiable
• Posted 1 day ago

A small but rapidly growing Medical Device company is seeking an experienced Regional Manager to cover the Netherlands. This innovative company has developed a completely unique system for treatment of chronic heart failure, which truly changes the lives of its patients. It has recently receiv...

• Plano, Texas
• Remote
• Posted 1 day ago

VP, Clinical Operations Pharmaceutical/Bio-Tech Hyper-growth Texas/Remote If you're looking for a change of pace this could be an amazing opportunity for you. As a firm looking to bring on Clinical Operations professionals, this could be an opportunity that allows you to work on novel science...

• South San Francisco, California
• US$30 - US$31 per day
• Posted 2 days ago

We are working with a large Biotechnology company in South San Francisco looking to add a Quality Specialist I to come join the team! This position will start as a 6 months contract. Quality Specialist I Primary Responsibilities Must be able to support establishment of GxP, SOP and Document...