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Biotech Operations Jobs

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Administrative / Operations Coordinator (Bio-Tech Co.) We are a small non-profit biotechnology company currently seeking an Administrative / Operations Coordinator to join our team on a Full-Time and Immediate basis. Successful employees promoted from this role previously have kept business activities organized and moving forward. The ideal candidate will perform a wide range of tasks related to ...

Job Summary:Primary designer and executor of deployment strategies for our client’s North American sales force.Working with the Director of Sales Operations, the Sr. Lead will build & analyze complex data models to quantify the value of accounts, carve out territories, and help negotiate territory changes with the sales management teams.Comfort with unstructured data and BI platforms are essential...

JOB FUNCTIONS / RESPONSIBILITIES The responsibilities of the Operations Manager include, but are not limited to: CPC MANAGEMENT -Complete induction and orientation for newly employed CPCs. -Ensure client-specific induction and orientation is planned, communicated and completed. -Establish goals and objectives for each CPC. -Monitor performance and conduct annual appraisal for each CPC, as ap...

Title: Sr Project Manager / BioTech Clinical Trial Operations (D1001)Location: Thousand Oaks, CaType: Contact – 1 year with likely extension(s) Overview: This position is part of a PMO group within drug development which supports and oversees clinical trials operations, R&D development, project management and business process improvement. Within R&D, this group supports the development side, inc...

POSITION: VICE PRESIDENT, CLINICAL OPERATIONS SUMMARY Reporting to the Chief Medical and Development Officer, the Vice President of Clinical Operations will have primary responsibility for overseeing the conduct of the clinical trials for the company's drug candidates. Serve as company clinical expert in investigator, medical advisory and regulatory meetings. Contribute to the set-up of clinical...

Title: Sr Project Manager / BioTech Clinical Trial Operations (D1001) Location: Thousand Oaks, Ca Type: Contact – 1 year with likely extension(s) Overview: This position is part of a PMO group within drug development which supports and oversees clinical trials operations, R&D development, project management and business process improvement. Within R&D, this group supports the development side,...

Homebased Opening! Need someone close to Raritan, NJ or Springhouse, PA - this is a HOMEBASED position but someone close by to their facility would be helpful as they will need to come in for meetings and etc. KEY NOTES: •Need someone who has been in a similar role before so they can jump into the role They don’t want to start from scratch to train someone how to do this specific job They hav...

Looking for a new Study Recruitment Manager for a Long Term Contract! Can be located in Springhouse,PA , Titusville, NJ or Raritan, NJ -This person will be accountable for the management,execution and delivery of patientand site initiatives for clinical trials.- Completion of patient recruitment, retention and informed consents. - You will work with different levels of management to be involved...

Immediate positon available for an experienced Business Procurement Coordinator with 2-3 years operational experience related to clinical trials with a pharmaceutical company and/or a CRO.Candidates must be able to demonstrate experience related to creation and management of vendor purchase orders, review and processing of vendor invoices, resolution of invoice mismatches and other detailed operat...

The PV Operations Leader will oversee all aspects of global individual case safety report (ICSR) collection, processing and reporting in accordance with applicable regulatory reporting requirements and company standard operating procedures (SOPs). Responsibilities Include: . Recruit, hire, train, manage and mentor a team of safety professionals responsible for processing, regulatory reporting an...

Our client is looking for a Head-Drug Safety Operations & Compliance. This position is located in the Monroe Township, NJ area. The position comes with good pay, bonus, benefits & paid time off. If you are looking to take your career to the next level, this position may be the one for you. The Head is responsible for managing, reviewing and providing regulatory oversight to all the drug safety se...

Our client is large medical device company looking for a Senior Lead, Sales Operations. Job Summary:Primary designer and executor of deployment strategies for our client’s North American sales force.Working with the Director of Sales Operations, the Sr. Lead will build & analyze complex data models to quantify the value of accounts, carve out territories, and help negotiate territory changes with...

This is a remote contract position for a great client.Clinical Operations Specialist will collect, accurately document, assess, code and process adverse event reports related to the marketed drug products monitored within the time frames established by the Department and in compliance with global regulatory requirements.In this role, the Specialist will serve as a primary contact point and recipie...

Senior Manager of Sales Analytics: My client, a specialty biotech company located in the SouthernCalifornia area, is committed to unlocking the potential biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. Their novel therapies have been used to treat more than 25 million patients. Their efforts are currentl...

Summary: To ensure that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for Good Clinical Practices (GCP) and International Conference on Harmonization (ICH).May be responsible for assisting the RA Department in the preparation, compilation, submission and maintenance of regulatory documentation required by international regulatory a...

Summary:To ensure that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for Good Clinical Practices (GCP) and International Conference on Harmonization (ICH).May be responsible for assisting the RA Department in the preparation, compilation, submission and maintenance of regulatory documentation required by international regulatory age...

About The Opportunity: This person will provide biostatistics leadership and oversight for all phases of clinical trials and drug development programs, including regulatory submissions. This individual is also responsible for production of biostatistics deliverables, such as statistical analysis plan and programming specifications in preparing a clinical study report (CSR) or publication. This I...

OBJECTIVE The employee will function as a Materials Coordinator in addition to assisting the Director of Materials with implementation, training and subsequent oversight of new programs, initiatives, software and systems. Employee will also assist with the generation and revision of documents that are specific to the Quality Management System. ESSENTIAL DUTIES/RESPONSBILITIES 1. Assist in monit...

Quality Systems Analytics Manager needed. Senior Manage of Quality Systems Analytics needed. We will be relocating to a new state of the art facility in New Haven in 2015. Exciting opportunity to join a biopharmaceutical company focused on serving patients with severe and ultra-rare disorders through the innovation, development and commercialization of life-transforming therapeutic products. We ar...

Quality Systems Analytics Senior Manager needed. Senior Manage of Quality Systems Analytics needed. We will be relocating to a new state of the art facility in New Haven in 2015. Exciting opportunity to join a biopharmaceutical company focused on serving patients with severe and ultra-rare disorders through the innovation, development and commercialization of life-transforming therapeutic products...