21-40 of 169 results
Sort By

- Cranford, NJ

Cranford, NJ, United States Full TimePOSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. This position is based in Client's Cranford, New Jersey office. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls,....


POSITION OBJECTIVE: Provide accurate, efficient and effective programming solutions required for clinical trial analysis and reporting. Perform a wide range of activities that include: understanding study protocols, study designs and SAP; creation of complex datasets, tables, listings and figures using SAS; follow and validate CDISC standards; perform basic quality-checklist code reviews; develop standardized programs to automate routine tasks; design, write and debug macro routines.....


Buffalo, NY, United States Full TimePOSITION OBJECTIVE: Provide accurate, efficient and effective programming solutions required for clinical trial analysis and reporting. Perform a wide range of activities that include: understanding study protocols, study designs and SAP; creation of complex datasets, tables, listings and figures using SAS; follow and validate CDISC standards; perform basic quality-checklist code reviews; develop standardized programs to automate routine tasks; design, write

- Pittsburgh, PA

My client is expanding and seeks a Scientist with aseptic fill experience. The ideal candidate will take on the following tasks:Support tech transfer and scale-up of products and processes to ensure smooth transition from process development into cGMP manufacturing.Assist with process-related issues and investigations.Participate in start-up efforts of new equipment and processes in manufacturing.Assist in documenting updates to manufacturing processes and working with manufacturing,....


POSITION OBJECTIVE: The Clinical Research Physician will be dedicated to providing a leadership role on a matrix team dedicated to stage appropriate clinical development of multiple innovative compounds. He or she will lead the development of clinical strategies for compounds and drive their successful implementation. This position is based in Client's New Jersey office. It is an office based position. Remote candidates will not be considered for this role. Essential Job....

- Cranford, NJ

Senior Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. . Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study....

- Cranford, NJ

As a Clinical Study Monitor, you will work within a clinical team setting to ensure study compliance with protocol, FDA and ICH guidelines. Essential Job Functions/Responsibilities · Ensure the Sponsor, Investigator, and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures. · Adhere to monitoring plan protocols; e.g. monitoring visit type, frequency, and required critical monitoring activities by utilizing monitoring....


The Manager, Medical Information will assist in the operational oversight of medical information within the Medical Affairs function under the guidance of the Lead of Medical Information. The manager will be responsible for providing and supporting the provision of accurate, scientifically balanced and timely responses to inquiries received from health care professionals, consumers and other customers. The manager will monitor the scientific literature and communicate new data to relevant....


Safety Physician POSITION OBJECTIVE: Supports the Pharmacovigilance team in reviewing, querying, documenting and reporting on all serious adverse events (SAE) & Suspected Unexpected Serious Adverse Reactions (SUSAR) cases related to clinical studies. Essential Job Functions/ResponsibilitiesProvide timely and sound medical review of individual case safety reports (ICSR) from clinical trials.Actively participates in the case initiation process (case triage) and case data inputting/data entry


Our client is a fast-growing established world leader in laboratory equipment and services, and has an opportunity for a Technical Sales Representative selling out client's line of microwave synthesis, extraction, and digestion instruments and will also include a line of Raman spectrometers. The territory includes OH, MI, KY, TN and IN. Candidates will ideally be located in Detroit, but other major cities in the territory will be considered. Qualifications:Must have a....

- Irvine or Madison NJ, CA

PLEASE NOTE THIS POSITION CAN BE BASED IRVINE, CA OR MADISON, NJ.Tope Tier Global Pharmaceutical company is expanding and adding a Director of Medical Science Library- competitive compensation package - including base, bonus, stock, and other incredible Long Term Incentives The Director of the Global Medical Science Library provides a vision for, leads, and is accountable for the administration, oversight, and propagation of this department, including the acquisition, planning, staffing, and....


This key leadership role in the Regulatory Affairs organization and will report directly to the Senior Vice President, Regulatory Affairs & Medical Writing. The incumbent in this role will lead the regulatory strategy group for the defined therapeutic area(CNS) to this position will provide expert leadership and managerial oversight for pre-approval and post-approval projects to ensure delivery of high quality regulatory strategy and submissions. Further, this position will guide....

- Adams, NE

HOT JOB ********* HOT JOB *********** HOT JOB ********** HOT JOB Working with chemical plant in need of technically strong production manager to help build culture. Our client is a state of the art facility. They opened the plant for business in 2006. Looking to grow output and need someone to help drive this challenge. Reports to a plant manager. The Production Manager is responsible for the operation of the plant to ensure production optimization and maximizing product quality along with....

- Lancaster, SC

We are looking for a Brand Manager who will be accountable for developing the brand innovation and communication strategies for a product (within a brand) to build consumer demand and market share. Brand Manager will be involved in development of brand strategy, pricing strategy, innovation, product portfolio management, new launches and integrated brand activation plans. The Brand Manager will plan and coordinate the retail marketing and promotional campaigns for assigned product lines. The....

- Boston, MA

My client is a rapidly growing firm, and they seek a Data Scientist to collaborate with the global data science group and provide innovative solutions. The ideal candidate will take on the following tasks:Provide data analysis support and lead in the design, analysis, and interpretation of translational research experiments.Offer statistical consultation to collaborators.Promote innovative study design and analysis methodology.Supply statistical input in planning translational experiments to....


Control Systems Integration firm is seeking an experienced Industrial Controls Engineer for their office in the Lenexa, KS area. Leading provider of control and systems integration solutions to manufacturers with focused experience in the food processing, pet food, pharmaceutical, plastics, specialty chemicals, ethanol / alcohol, and feed and grain industries. The company's specialties include high-end batching systems, automated cooking extrusion, food and ingredient processes, metal forming,


Control Systems Integration firm is seeking an experienced Industrial Controls Engineer for their office in the Lenexa, KS area. Leading provider of control and systems integration solutions to manufacturers with focused experience in the food processing, pet food, pharmaceutical, plastics, specialty chemicals, ethanol / alcohol, and feed and grain industries. The company's specialties include high-end batching systems, automated cooking extrusion, food and ingredient processes, metal forming,


Process Controls Engineers with DeltaV experience needed for reputable award-winning Automation and Control Systems Integration company. Great chance to use your industrial automation experience within the Biotech, Pharmaceutical, and Food and Beverage industries. Why work here?:Stable business for 25 years and growing!Fun and professional environment with over 120 employees!Variety of projects in several industries, many pharmaceutical and biotech projects!Training provided on new technology....


Growing Industrial Automation Systems Integrator seeking Controls Project Engineers for their Indianapolis area office. Why work here?:20+ years in business with several offices in the Midwest85% repeat business with existing client baseVariety of projects in Pharmaceutical, Automotive, Food & Beverage, Consumer Goods, General ManufacturingAll engineers have cradle-to-grave involvement with their projectsAll Managers and Owners have worked as an Engineer in their careerKnown in the....

- Raleigh, NC

Controls System Engineers needed in Raleigh, NC for Control Systems Integrator and panel shop doing projects in a variety of industries including water/wastewater, agricultural, pharmaceutical, and general manufacturing. Why work here?:Family-oriented environment close to downtown Raleigh Be involved in all stages of a project including design, programming, start-upLow overnight travel - about 5%Great benefits and overtime pay if over 40 hours/week!Requirements:BS degree in Engineering3+....

21-40 of 169 results