We are seeking an exceptional, highly motivated early-career multidisciplinary data scientist/computational biologist to work in a collaborative environment, partnering closely with our functional genomics and data science groups to design experiments, analyze results, and develop analytic solutions to address underlying biological questions in a high-throughput manner. The successful candidate...

The Quality System Specialist, under the direction of the QS&C management team, will be responsible to support the global Quality Systems and their operations in ensuring compliance and fit for intended use in accordance with applicable global SOPs. Position details: • Assist in the governance of Quality System applications, including harmonization of processes across sites • Assist in...

General Summary Installs, calibrates, repairs and inspects imaging devices, robots, and computers and solves moderately complex problems in the field. Performs repairs up to and including the diagnosis and repair of difficult technical instrument and software problems. Participates in product improvement discussions, and provides inputs to design engineering. Provides information and develops...

 Precision Life Sciences is working with a client seeking various Stat Programmers from Sr. Manager to Assistant Director to Director.  These roles are remote or hybrid and are contract-to-hire or direct hire. Overall responsibilities include: • In collaboration with the Statistical Programming therapeutic area units (TAUs) lead, these positions serve as key contributors to the development of...

Our client, in the Life Sciences industry, is seeking a Director, Business Development Consultant to be a key driver of partnering activities and corporate strategy. The person will report to the SVP of Business Development and will have the opportunity to lead numerous complex projects forward simultaneously. In this high visibility role, the Business Development Director will gain first-hand...

Seeking a Head, Quality Assurance who will be responsible for developing and maintaining appropriate quality systems related to GxP-related activities. Reporting to the Chief Development Officer, you will be responsible for ensuring compliance across GMP, GCP, and GLP activities. This will include the manufacture and packaging of clinical materials (GMP), execution of clinical trials (GCP), and...

Our client is seeking a contract Research Scientist. The client has an excellent opportunity for a highly talented biologist with a strong background in cell / molecular biology. The scientist level position is currently as a contract research scientist for 12 months with the possibility of renewal. We are seeking a highly motivated and interactive bench scientist to join our team focused on...

Our client is seeking a contract Senior Research Associate. This client has an excellent opportunity for a highly motivated biologist with a strong background in cell / molecular biology. The Senior Research Associate, Biology position is available currently as a contractor for 12 months with the possibility of renewal. We are seeking a highly motivated and interactive bench scientist to join...

The Electronic Trial Master File Specialist (eTMF Specialist) is responsible for the day-to-day management of eTMF, including oversight of the review and approval of eTMF documents and generation of reports to measure completeness, accuracy, and timeliness of the eTMF. This role has a strong focus on ensuring that document management operations are performed with adherence to ICH-GCP guidelines,...

Summary: The Senior Regulatory Affairs Specialist will execute regulatory activities to support currently marketed devices and new product development. This role involves a multi-faceted set of skills including sound regulatory judgment, cross-functional collaboration, and planning/oversight/execution of projects & activities that directly impact the operational results of the business.   ...

The Medical Monitor will serve as the contact for an Investigator site and provide expertise for answering questions and resolving study-related issues. The Medical Monitor will often be responsible for several different studies, potentially across TAs, covering a region, and will need to perform AE reviews and assist other Site Management staff with medical issues/questions and local regulatory...

Our client is seeking a contract, remote Senior Medical Writer. The Senior Medical Writer independently plans and prepares a variety of clinical documents necessary for all phases of clinical drug and device development by organizing, analyzing, and interpreting scientific and statistical data. Such documents include Module 2 clinical summaries of marketing applications, integrated summaries of...

Our client, in the biotechnology / life sciences industry, is seeking a Senior Manager, Statistics (contact to hire). The purpose of this position is to provide compound level/development phase statistical expertise and leadership by: • Independently designing, analyzing, and interpreting clinical or observational studies at a compound level for early phase or less complex programs. •...

Our client is seeking a Senior Director, Biostatistics for a 6-month remote contract. The Senior Director, Biostatistics is responsible for the successful operation of the Biostatistics department, overseeing the statistical aspects of projects and project teams through the management of department managers, internal staff, and interaction with Executive-level staff. They oversee the maintenance...

KEY RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO: · Analyzing products to determine chemical and physical properties following Company, client, and pharmacopeial methodologies · Performing method development for potency and impurity/degradant analysis using GC, HPLC, UPLC, or LC/MS instrumentation · Ensuring work is performed in compliance with standard operating procedures, good laboratory...

Our client is seeking a Principal Medical Writer for a remote, 6-12 month contact. This role independently plans and prepares a variety of clinical documents necessary for all phases of clinical drug and device development by organizing, analyzing, and interpreting scientific and statistical data. Such documents include Module 2 clinical summaries of marketing applications, integrated summaries of...

We are working with a client, in the life sciences industry, that is seeking a Manager, Research & Development Quality, Quality Management System (QMS) who will be responsible to assist with the development and ongoing support of the QMS for the Research and Development organization including but not limited to GxP (GLP, GCP, GVP & CSV) Policies and Procedures, Knowledge Management, Issue...

Our client is seeking a remote, Data Mining Specialist. The role is responsible for data mining of internal clinical study reports for data extraction; including curation and digitalization for export to an existing database.  Required skills: • Basic knowledge of immunology • Minimum 3+ years experience with data mining  Critical skills: • Data mining • Data digitalization • Basic...

We are working with our client, in the Life Science / Biotechnology industry, to bring a Formulation Technician onboard. KEY RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO: · Preparing formulation records and manufacturing formulations using mixing, blending, granulating, and compression laboratory equipment · Performing physical characterization of formulations using test instrumentation...

We are working with our client, in the Life Science / Biotechnology industry, to bring a Formulation Research Scientist onboard. KEY RESPONSIBILITIESINCLUDE, BUT ARE NOT LIMITED TO • Developing and analyzing both liquid and solid formulations for client companies • Designing and performing experiments in the development of new, proprietary drug delivery and other technologies •...

Our client, in the life sciences industry, is seeking a remote Director, Technical Operations. This position is responsible for initiating, coordinating, and completing technical projects as assigned. These projects may involve but are not limited to: validating a manufacturing process, scale-up/transferring a new product/process into production or to a contract manufacturing site, troubleshooting...

We are seeking a collaborative and science-driven global regulatory expert who wants to work with innovative investigational medicines. You will lead a global regulatory team to develop and execute regulatory strategies for high-impact projects while working with decision-makers across multiple functional areas. Responsibilities As a Director, Global Regulatory Lead, on one or more projects you...

Our client, in the Life Sciences industry, is seeking an Analytical Scientist. KEY RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO: · Analyzing products to determine chemical and physical properties following Company, client, and pharmacopeial methodologies · Performing method development for potency and impurity/degradant analysis using GC, HPLC, UPLC, or LC/MS instrumentation · Ensuring work...

Our client, in the biotechnology industry, is hiring a VP/SVP, Regulatory Affairs and Quality Assurance.  This role is accountable for playing a vital role in progressing our drug candidates towards U.S. and International approval. The VP/SVP is a highly effective leader and mentor, who leads regulatory affairs and quality assurance to provide high-quality logistical support for our programs.   ...

Our client is seeking a strong scientific and strategic leader to head the clinical flow cytometry efforts. The Head of Oncology and Cell Therapy Flow Cytometry is an exciting, new role within the growing Precision & Translational Medicine (PTM) function in the Oncology Therapeutic Area Unit (OTAU) reporting to the Head of Clinical Biomarker Sciences and Operations. The individual recruited for...

We are working with our client, in the Life Science / Biotechnology industry, to bring a Formulation Research Engineer onboard. KEY RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO: • Building and maintaining development equipment, including setup, operation, disassembly, cleaning, calibration, and training • Designing and performing experiments in the development of new, proprietary drug...

Our client, in the biotechnology / life sciences industry, is seeking an Associate Director, Statistics (contract to hire). POSITION ACCOUNTABILITIES: • Serve as global statistical lead for biomarker development in Oncology Cell Therapy and TA. Provide statistical leadership and support for internal decision making, regulatory meetings, submissions, and follow-up. • Review key program...