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- Los Angeles, CA
new job!

Data Scientist JOS000000705 Full-Time/Regular EmploymentDegree in Statistics or related fieldPrior experience as Data ScientistCompany is experiencing rapid growth.Experience with financial transaction data.Payment industry experience is a plus.R, PythonSAS, SPSSDevelop rules and models to detect risk in portfolios.Multivariate Regression, Logistic Regression, clustering algorithms, Support Vector Machines, Decision TreesPredictive ModelingRelocation assistance may be available.Targeting....

- Bridgewater, NJ
new job!

This position is in the Research & Development department at the corporate level, to support Global business category in its portfolio development activities. Closely collaborates with the other team members of the Global Regulatory Cough & Cold and Allergy category working on Allergy portfolio, in order to ensure the development of robust programs for global projects including the non-US requirements for the innovation projects. Responsibilities:Work with Region North America (NA) and

- Ivine, CA
new job!

Responsible for supporting the Clinical Trial Management/operational study team to manage the various aspects of the operational execution and delivery of quality studies, including in process quality control activities.

- Irvine, CA
new job!

WPIJP00008461 - Clinical Trial Manager 09-24-2018 to 09-23-2019 WPIJP00008485 - Clinical Trial Manager 10-01-2018 to 03-15-2019 These are contingent worker situations expected to last 1 year. Qualifications - B.S. degree. - Minimum of 3 to 5 years of pharmaceuticals/biotech experience. - Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials. - Process and system....

- New Jersey, NJ
new job!

Plan and prepare complex medical device regulatory submission documents for US, Canada, and EU regulatory filings. Provide support for other global regulatory filings. Utilizing detailed, in-depth understanding of medical device regulations, leads and participates in global regulatory teams, interprets regulations, and provides regulatory guidance. Supports management with regulatory programs planning and implementation of departmental strategies and policies.

- Menlo Park, CA
new job!

Qualifications - 12+ years of proven experience in clinical research and/or clinical trial operations, including a minimum of 7 years in a supervisory role managing (internal/external) clinical operations staff. - Industry experience within pharmaceutical and/or biologics and prior experience in FDA negotiations relating to the conduct of regulated clinical trials. - Comprehensive understanding of applicable clinical research regulations. Thorough knowledge of GCP, ICH guidelines and other

- Menlo Park, CA
new job!

Our client seeks a Clinical Research Operations professional to plan their Phase I Clinical Trials Requirements Bachelor’s Degree in life sciences or healthcare field. Additional coursework in clinical trial design.Ability to travel as required (up to 25%).12+ years of proven experience in clinical research and/or clinical trial operations, including a minimum of 7 years in a supervisory role managing (internal/external) clinical operations staff.Industry experience within pharmaceutical....

- Northern, CA
new job!

Responsibilities Manage, develop, and train the GCP Compliance personnel. Ensure the integrity and quality of clinical data by overseeing all routine and directed; internal and external; domestic and international GCP audits and quality reviews. Promote continuous improvements in quality systems and department infrastructure. Act as a subject matter expert and provide GCP guidance to internal departments for all phases of clinical development. Report significant and/or serious ongoing quality....

- Richmond, VA
new job!

Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. They have an opening for a Lead Scientist – Raman Spectroscopy who will be based in the Richmond, VA area. The Lead Scientist applies scientific knowledge and principles to provide in-depth training and assistance to sales staff and customers on the proper use of highly complex measuring and laboratory instruments. This important position will represent the company as....


Our client is a world leader in laboratory equipment and services and has an opportunity for a Technical Sales Representative (TSR) for its industry leading analytical instrumentation used in R&D laboratories. The Technical Sales Representative will be responsible for direct sales of mechanical surface characterization instrumentation and services to customers covering GA, FL, AL, MS and the Caribbean with an ideal base in Georgia or Florida. The product lines include atomic force....

- Sacramanto, CA
new job!

Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they are adding a new Field Service Engineer to be based in the Sacramento, CA area. The Field Service Engineer provides on-site service including preventative maintenance, calibration, installation, and training across all product lines.Responsibilities & QualificationsThis position will be based in or near the Sacramento, CA area but will


We are looking for an experienced Environmental Water Quality Program Specialist (Project Manager / environmental lab / analytical). Duties and Responsibilities : Project set-up, Sample Receipt, Reporting, Account Maintenance- Provide courteous and efficient telephone and e-mail support to clients; Schedule/coordinate access and/or on-site escort for field staff; Interface/liaison between the lab and internal and external customers; Works with Lab Operations to ensure adequate capacity and....


Great opportunity to join a global industry leader, as the champion for strategic development and management of the Global Bioinformatics Group. As the Group Leader, you will drive the innovation of bioinformatics and genomics capabilities for research, development and delivery of products for multiple sites. The successful Leader will have a Ph.D in bioinformatics, genomics, or computational biology, and 10+ years experience in industrial biotechnology or related Industrial R&D life....


Strategic opportunity as North American (NA) Team Leader supporting Analytical/ Synthesis (Methods Development); Product Metabolism, Product Safety (registration); and Regulatory Compliance (EPA). Participate on the Global Leadership Team while developing a challenged, problem-solving analytical team responsible for performing/ delivering scientific studies to ensure a sustainable product safety and registration success. The successful candidate will have a strong background in Scientific....


Senior Analytical Chemist Location: Rockland County, NY (Near Ramapo, Nanuet, & Tappan NY and Park Ridge NJ) Unable to publish the full confidential salary range but we can talk about it! ( I filled in the low salary box but not the high level) An opportunity for a Senior Lead Analytical Chemist to support a process development effort. This is a critically important position since ‘reliable data’ is a key to success as they work to develop a novel process. The position will include a....

- Any US State

RETAINED SEARCH - Dir Regulatory Affairs - Safety & Efficacy MUST have Animal Health Pharma experience Prepare Review Reg submissions FDA - CVM - INAD's - CFR - ICH/VICH - RAPS Prefer Advanced degree or DVM Virtual Office - Work remote


Our client is a world leader in the manufacturing and distribution of analytical instrumentation used in R&D Laboratories. Due to continuing growth they are adding a new Field Service Engineer to be based in the Indianapolis area. Requirements:Duties include the preventative maintenance, troubleshooting, repair, and calibration of instruments in the assigned region.Managing inventory and reporting for accuracy.This position requires up to 75% overnight travel within the Midwest and....


Represents Regulatory Affairs for pharmaceutical development projects and marketed products. Responsible for development and communication of all aspects of global regulatory strategy on R&D project teams. Leads team of regulatory professionals to assure successful planning and completion of regulatory activities on a worldwide basis. Responsible for knowledge of regulatory requirements of major regions (e.g. US, EU JP) with responsibility for working with colleagues on a worldwide basis....

- Any US State

The role of the Principal Writer, Medical Writing, is to prepare high quality clinical documents and to oversee medical writing responsibilities for multiple programs within an assigned therapeutic area (TA) of Global Branded R&D (including, as appropriate, drugs, biologics, and devices). In this position, the incumbent manages the planning and preparation of high-quality clinical documents (eg, clinical study reports, briefing books, clinical protocols, integrated summaries) and ensures....


Regional Quality Leader for R&D the Americas, and is accountable for the oversight, direction and management of R&D Quality site operations and projects within the Americas. This role provides business partnership to R&D leaders to ensure that appropriate systems, procedures and resources are in place for effective execution of the R&D quality system. Functions, Duties, Task - Responsible for the execution of the global Quality Assurance and Compliance Strategy for R&D....

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