Temporary, Contract, Project 8888 mortgage underwriting quality analyst jobs in the Biotech, R&D, Science category

The Senior Quality Analyst will manage outsourced QC testing functions at contract laboratories and contract manufacturers for late stage clinical development programs. Responsibilities will include: Manages transfers and validations for in-process and release testing methods at contract sites Review in-process and release testing results from contract laboratories in conjunction with batch dispos...
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Global Pharmaceutical company is seeking a Compliance and Analytics consultant for a contract position for a minimum one year contract. Analyst will provide site perspectives to the Quality Safety Team Leads with adherence to safety, regulatory, and project timelines, bridges partnership with customers to support “in line” quality ownership and participates in the development of efficient tools an...
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Data Analyst/Programmer is needed for a 9month contract. • Support a KPI reporting system to provide the business with meaningful metrics that will drive continuous improvement • Ensure that any updates to data that are required to bring a source system into compliance is communicated to the source system owner • Establish a sound working relationship with source system owners (including Logistics...
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We are looking for a Statistical Analyst in the San Jose area that specializes in SAS to work at our client, a high technology GIANT. The role will support Marketing and Sales' high level objectives for acquisition, retention, wallet share improvement, and profitability by identifying, designing, and implementing advanced analytic projects utilizing techniques such as statistical and algorithmic m...
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Pharmaceutical Staffing Solutions (a division of Jeiven Pharmaceutical Consulting, Inc.) is currently seeking experienced Quality Consultants to work in New York Metropolitan area. We are seeking individuals with experience in development and manufacturing of finished pharmaceuticals (familiarity with 21 CFR Parts 210 and 211) or those with experience in manufacturing of dietary supplements (famil...
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. We are currently looking to hire a Quality Complaints Co-coordinator with experience in the medical device industry. This is a long-term contract on Andover, MA. Please email your resume to Todd.Schecter@AdeccoNA.com for review. Note: This is a Jr-Mid level role Responsibilities: Lead product complaints investigations and ensures investigation action plans and final investigation summaries are a...
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The Clinical Scientist is responsible for the scientific strategy of assigned clinical trials for protocol development, ensuring the review/reporting of quality trial data, and study reporting/publishing in compliance with processes, GCP/ICH and regulatory requirements. Supports program level activities as assigned. Program/project level responsibilities: • Support the development of operational p...
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. Adecco Medical and Science, a division of the world leader in the recruitment of medical and scientific professionals, has an immediate opening for a Clinical Research Associate on a 8+ Month contract opportunity in Irvine, CA. Responsibilities: Ensures all site related activities and files are completed per the SOPs Employee is a key point of contact for study specific questions from both inter...
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COMPANY PROFILE Sound Advice is a boutique consulting services firm headquartered in New York with a national presence. We have a reputation for quality and excellence in the Pharmaceutical and Life Sciences space. Sound Advice has a long term strategic partnership with one of the world’s largest and most respected Pharmaceutical companies, headquartered in New York City. We have been engaged to p...
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This position reports into Head of Global Sourcing Area and works within Procurement across legal entities and national boundaries with a strong focus on procurement strategy and service delivery. This position would provide contract support within a therapeutic or division specialty. This position will also support the identification, selection, and management of suppliers and contracts across th...
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Manager (Safety Physician) Responsible for the continued safety assessment, evaluation and risk management of major company products or product groups in clinical development and/or the post-marketing setting Ensures that adverse event and other safety information is efficiently evaluated in order to meet global compliance and regulatory requirements, identify the need for product labelling update...
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Sr. Study Manager The Study Manager is responsible for • Leading one or several cross functional study teams (and/or sub-teams) to deliver clinical research studies on time, within budget and with good quality in compliance with Regulatory Authorities regulations/guidelines and Celgene SOPs/WPs. • Sharing best practices • Contributing to process improvement initiatives Study Manager Responsibiliti...
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You've imagined it many times. You're working at a company that challenges you to innovate and encourages you to apply your talent and knowledge. Where you're empowered and expected to make decisions that propel business growth. Where you receive compensation worthy of your sterling accomplishments. If that's your vision, but not your current reality, Experis has a career opportunity for you. You ...
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Job Title: Clinical Trial Leader Position Description Accountable for all aspects of assigned OTM clinical trials (Phase I/II) including leading Clinical Trial Team(s) (CTT). Number of clinical trials depends on the workload and complexity of the individual trials. Responsible for program level activities as assigned. Position Responsibilities Lead the clinical protocol development process in coll...
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Job Title: Clinical Trial Head Position Description Accountable for all aspects of assigned OTM clinical trials (Phase I/II) including leading Clinical Trial Team(s) (CTT). Number of clinical trials depends on the workload and complexity of the individual trials. Responsible for program level activities as assigned. Position Responsibilities Lead the clinical protocol development process in collab...
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The selected candidates will focus on developing original validation plans per 21CFR protocol documents including Installation Qualifications (IQs), Operational Qualifications (OQs), Performance Qualifications (PQs), and Process Validations (PVs) for equipment qualification and process risk management / FMEA. Equipment to validate includes: FT-IR, viscometers, moisture ovens, refractometers, etc. ...
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. Exciting direct hire opportunity for a Full Time Clinical Research Associate in Pleasanton, CA! Responsibilities include: Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects; May co-ordinate the activities of relevant colleagues within the Company and investigators to ensure compliance with the overall scie...
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Job Title: Inform Database Developer Position Responsibilities Plans, directs, and manages the clinical database design and maintenance process. Reviews the protocol and associated reference material and develops the database design project timeline. Maintains database design timelines. Promotes good project management practices. Conducts project initiation meetings with the database design team t...
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. Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has an immediate opening for a SAS Programmer with Pharmaceutical and Clinical Trials experience for a contract position in Bridgewater, NJ RESPONSIBILITIES: Knowledge of FDA regulations (21 CFR part 11) and guidelines in new drug development and application process re...
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Contract Assignment – H-1’s/Subcontractors will NOT be considered: · Responsible for compliance with quality system regulations. · Complies with all policies, established procedures, and regulations related to clinical research. · Actively participates as a member of the crossfunctional project team. Leads a clinical project from study inception to completion. · Participates in assessing performan...
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. Adecco Engineering and Technical, a division of the world leader in the recruitment of scientific and engineering professionals, has an immediate opening for a SAS Programmer with Pharmaceutical and Clinical Trials experience for a contract position in Bridgewater, NJ RESPONSIBILITIES: Knowledge of FDA regulations (21 CFR part 11) and guidelines in new drug development and application process re...
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Sr. Statistical Programmer The Sr. Statistical Programmer will provide timely support to the study team on all programming matters according to the project strategies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. Should have the ability to generate all of the production tables needed for a given stu...
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Shall provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data. Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical. statistical reports and other similar reports. Contribut...
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Large CRO is seeking an Associate Clinical Data Manager for a long term contract opportunity in Overland Park, KS. Client requirements: 5+ years experience in Data Mgmt including managing project timelines, quality issues, resource mgmt, CRF design, discrepancy mgmt, locked databases, study start up through database locks. The candidate will mentor other team members and Lead Data Managers in trai...
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Currently we have a temporary opening for a Sr. Technician to support a company located in the Stamford, CT area. Responsibilities: Manage and develop ingredient specifications/procedures/computer systems (i.e. Optiva). Maintain supply base and ingredient management system Interact with Procurement/QA/Development/Ingredient Vendors/Technology/Production Communicate quality requirements for ingredi...
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