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Ardea Biosciences/Astra Zeneca…NOW HIRING...Sharepoint Administrator, San Diego, CA Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is searching for a Sharepoint Administrator to join the team. The overall responsibility is to provide support and administration of corporate Intranet and Extranet, and daily support ...

2013…..NOW HIRING in San Diego….Sr. Scientist/Scientist, Analytical Sciences…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking a Sr. Scientist/Scientist, Analytical Sciences to join its dynamic team. We are seeking a Senior Scientist/Scientist, Analytical Sciences who will ...

2013…..NOW HIRING in San Diego….Senior CMC Regulatory Associate…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking a Senior CMC Regulatory Associate to join its dynamic team. We are seeking a Senior CMC Regulatory Associate who will assists in planning, reviewing, and preparing ...

2013…..NOW HIRING in San Diego….Contract Sr. Clinical Research Associate…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. We are seeking a Senior Clinical Research Associate (Sr. CRA) who will support efforts to design, plan, monitor and execute clinical research project(s) and is ...

2013…..NOW HIRING in San Diego….Lab Technician, Bioanalytical…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea Biosciences currently has an opening for a lab technician in the Bioanalytical section of our Translational Sciences Department. This position will perform sample handling, ...

2013…..NOW HIRING in San Diego….Contract Clinical Research Associate…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. We are seeking a Clinical Research Associate (CRA) who will support efforts to design, plan, monitor and execute clinical research project(s) and is accountable for ...

 Founded in 2007, Millennium Laboratories has become the leading research based clinical diagnostics company dedicated to improving the lives of people suffering from pain. We are dedicated to alleviating pain and suffering by helping healthcare professionals improve clinical outcomes and patient safety. Recognizing the unique needs of the industry, we provide healthcare professionals total choice in urine and oral fluid drug testing backed by unsurpassed customer service, education and ...

Millennium Laboratories is the leading research-based clinical diagnostic company dedicated to improving the lives of people suffering from pain and/or addiction.  We provide healthcare professionals with the medication monitoring and drug detection services, clinical tools, scientific data and education helping to personalize treatment plans to improve clinical outcomes and patient safety.   We provide customized drug testing services for healthcare professionals to help them to mitigate the abuse ...

 Description Candidate must be dedicated to addressing and solving some of the most important unmet medical needs in cardiovascular and metabolic diseases.   We work to bring innovative ideas, products, services and solutions to individuals with serious conditions, and to physicians throughout the world. We are nurturing an environment of performance excellence, built on trust, respect and accountability. Through an emphasis on strong leadership and people development, we will accelerate our sales ...

DUE TO THE NUMBER OF POSITIONS AND SITES THERE SEVERAL OPEN AREAS.  THESE POSITIONS CAN BE LOCATED IN CA, AZ, the MID WEST, NY, NJ, and NORTH WEST   A minimum of a BA/BS degree is required. Degree in a health or science major. Minimum 5+ years oncology monitoring experience. Estimated 70% travel. Minimum 6+ years pharmaceutical experience is required. Should have solid understanding of the drug development process including GCP and FDA Code of Federal Regulations. Solid communication and computer ...

Millennium Laboratories is the leading research-based clinical diagnostic company dedicated to improving the lives of people suffering from pain and/or addiction. We provide healthcare professionals with the medication monitoring and drug detection services, clinical tools, scientific data and education helping to personalize treatment plans to improve clinical outcomes and patient safety. We provide customized drug testing services for healthcare professionals to help them to mitigate the abuse and ...

Millennium Laboratories is the leading research-based clinical diagnostic company dedicated to improving the lives of people suffering from pain and/or addiction. We provide healthcare professionals with the medication monitoring and drug detection services, clinical tools, scientific data and education helping to personalize treatment plans to improve clinical outcomes and patient safety. We provide customized drug testing services for healthcare professionals to help them to mitigate the abuse and ...

CRAs - Join Covance and receive a$5000 Sign On Bonus!     Experienced Clinical Research Associates (CRAs)/Monitors: We are hiring Phase I-IV CRA positions.    Positions are home-based and needed throughout the United States.   All therapeutic areas needed.  Please let us know if your experience includes Diabetes -Type I/II, Oncology, CNS, Inflammatory, Cardiovascular, and Respiratory. Focusing on balance and quality by only working on 1 to 2 studies!   Our Clinical Research Associates ...

Clinical Enrollment Manager - Contract - Home Based     The Clinical Enrolment Manager will be responsible for providing on site recruitment and ensuring good working relationships with sites to enhance enrolment opportunities. The core focus will be on the CEM to help improve the recruitment rates. There is a high level of travel required with this position, so potential CEM’s must be willing to travel 4 days a week. Key Accountabilities: - Maintain updated patient database plus regular site contact ...

Job Responsibilities and Requirements: Key Deliverables: Lysis of cell pellets (e. coli and insect cells) using defined buffers Perform standard chromatographic separations (SEC, IEX, Ni-affinity) using defined buffers Analyze protein purity by SDS-page gel electrophoresis Determine protein concentration using standard spectrophotometer methods Enter corresponding data into LIMS database and maintain laboratory notebook according to defined protocol Prepare and store bar coded protein samples Basic ...

Shall provide expertise for the development and implementation of global strategy involving drug discovery initiatives, clinical development, pharmacogenomics, clinical pharmacology, biomarker strategies, companion diagnostics, and personalized medicine strategies. Ensure smooth transition between discovery, development, preclinical testing, and early clinical studies through proof of concept MD or MD-PhD and 10+ years relevant experience with a major pharmaceutical company required. Highly ...

Seeking In-depth pharmacokinetics and pharmacodynamics experience and track record driving drug candidates through the development process and more specifically guiding pulmonary therapeutics through regulatory submission, review and post marketing commitments to plan and oversee clinical studies, analyze results, write study reports, develop regulatory documents, interact with regulatory agencies, report progress to partners and investors, and serve as Medical Monitor. Required: *** Ability to ...

We are a small biopharmaceutical company located in San Diego, CA in the Torrey Pines area. Our exciting product is entering late phase clinical trials. We are looking for a hands-on Quality Assurance Sr. Manager/ Director to lead the quality functions for the overall Quality Assurance Unit. This role collaborates with the GXP (GMP, GLP, and GCP) functional areas in order to ensure quality and compliance in all GXP-related activities. An immediate emphasis on CMC (chemistry, manufacturing and ...

This is a permanent position. Must have recent oncology experience. West Coast CRA to be located anywhere West Coast (CA, NV, AZ, OR, WA). SOLID work history; 3 years monitoring exp. minimum Job Key Duties and Responsibilities: This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor: Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory ...

Position, Location The Director or Vice President of Scientific Affairs will lead the company’s strategic efforts in developing novel therapeutics in both cardiovascular and cancer fields through internal development and external scientific collaborations. The position is located at Zensun USA, Inc. in San Diego and needs actively working with the teams in the Company Headquarters in Shanghai, China. Specific Responsibilities  Design and execute a comprehensive plan of scientific / clinical ...

Quality is critical in the manufacturing of drug products. Allermed is seeking an individual to provide Quality Assurance oversight of the Analytical Quality Control Laboratory and Quality Assurance function for the manufacture of licensed biologic products. The position reports to the Chief Operating Officer. The major responsibility for this position is two-fold. 1. Oversight of the Quality Control laboratory requires an individual who has had analytical laboratory experience and feels ...

2013…..NOW HIRING in San Diego…. Medical Director…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea Biosciences is seeking a Medical Director who will participate in the development and implementation of the organization’s clinical development strategy for our gout franchise, for US and ...

2013…..NOW HIRING in San Diego….QA Manager Validation…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is searching for a QA Manager, Validation to join the team. The successful candidate will assure software validation compliance with applicable regulatory requirements including ...

Ambrx is a biopharmaceutical company enabling a new field of protein medicinal chemistry, using a fundamentally new technology that directs incorporation of amino acids beyond nature’s conserved set into biosynthetic proteins to produce high value biologics products. Ambrx is seeking a highly motivated scientist to be a key member of a fast-paced and dynamic organization. As part of a team, the ideal candidate will produce therapeutic proteins in mammalian cells and to help mature Ambrx’s ...

Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases We are seeking a medical writer who will be responsible for writing and/or revising regulatory documents in support of drug development, including clinical protocols, clinical study reports, patient narratives and investigator brochures. Responsibilities include: •Write and/or ...

Please Note - Candidate will be required to be onsite. Responsibilities - Writing and review of protocols and/or reports for manufacturing process characterization studies - Writing of protocols/batch records for manufacturing process validation - Writing and/or review of other CMC documents as needed - All activities will need to be performed in close collaboration with key team members Skills/Experience: - Excellent technical writing and reviewing skills for process development and ...

Experienced Product Manager will provide marketing insight and direction to optimize new product launch. Will be responsible for developing marketing strategy, product positioning and pre-launch and launch plans for a first-in-class oncology immunotherapeutic. Responsibilities: •Perform strategic market analysis including market size and drivers, segmentation analysis, competitive landscape, opportunities and factors for success. Translate results into product positioning and marketing strategy. ...

Description/ Responsibilities: Application engineering POC for Mobile Broadband data products including but not limited to embedded WWAN modem modules, USB dongles, WiFi hotspots, Wireless CPE, etc. The POC will work at NA R&D Center MBB Product which is a remote technical team to interface with HQ, Ecosystem, Customer Reference Design Teams, and occasional technically support onsite to customers. •Responsible for North America customer platform reference design WWAN integration, including co ...

2013…..NOW HIRING in San Diego….Director/Sr. Director, Regulatory & Scientific Communications…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. The successful candidate will be responsible for managing and directing the medical writing function as well as producing documents for regulatory ...

We are currently looking to hire Permanent Regional CRAs Job Description   The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification ...

Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking a GCP QA Manager/Senior Associate to join it's dynamic team. The successful candidate will provide consultation in interpretation of GCP regulations, guidelines, policies, and procedures; plan and conduct independent Good Clinical Practice (GCP) quality ...

 This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor:   Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects Conduct Pre-Study Site Visits (or calls), Study Initiation ...

Novartis Pharmaceuticals Description: To investigate the role and therapeutic applications of cellular aging and senescence. Contributes to the leading drug discovery projects and intiates new lead discovery projects targeting established and novel molecular pathways. Responsibiities include fostering scientific and operational excellence, supervising associates, developing and optimizing biochemical or cell-based assays for hit identification and lead optimization. Requirements: Ph.D. or M.D ...

The HR/Talent Manager is primarily responsible for the talent management function. This responsibility includes developing effective and creative sourcing strategies; building and maintaining a diverse pool of top talent; focusing on targeted recruiting, social media branding, employee onboarding, training and development needs, and retention; industry networking and building/maintaining relationships; managing the ATS; participating in employee relations issues; and other HR related tasks as needed. ...

Millennium Laboratories is a national, research-based medication monitoring company whose test panels, technology, customer support, educational resources and experts are specifically focused on clinicians who treat chronic pain. We utilize the latest cutting-edge technology, Liquid Chromatography/Mass Spectrometry/Mass Spectrometry (LC-MS/MS). This allows Millennium to provide the fastest turn-around time in the industry for determining the presence and precise levels of drugs in a patient’s urine, ...

Develop and implement strategies focused on molecularly driven oncology programs integrating data from clinical trials, journals and medical records into biomarker development, discovery research, patient selection and clinical research. Collaborate with clinical personnel, research teams, academic institutions and other scientific professionals to drive the development of novel therapeutics. Qualifications: *** MD, MD-PhD or PhD in a relevant scientific field such as pathology, molecular biology ...

Strategic leader needed to oversee a program in cancer immunotherapy with a focus on translating findings from preclinical studies into the design and implementation of collaborative clinical trials. Shall: *** Lead the review, analysis and interpretation of study data to develop preclinical strategies for biomarker discovery *** Provide scientific expertise for evaluation of licensing opportunities *** Establish collaborations and interact with external clinical groups to drive the ...

Our client, a leading biopharmaceutical company, is looking for a Lab Technician to join their team. Responsibilities: Routine small animal husbandry, animal health monitoring, cage changing, sanitation and operation of the cage washer and autoclave. The work may include occasional holiday and weekend duties. Qualifications: Requires a high school diploma or equivalent. Experience with small animal husbandry and ability to follow established SOPs. Must be able to lift 50 Ibs. Experience with ...

Our client, a water service company, is currently seeking a Laboratory Technician to join their team. This person will be responsible for conducting laboratory tests for chemical and bacteriological analysis of potable and raw water, and treated wastewater. DUTIES • Collects potable and recycled water samples from specified locations in the distribution systems and Water Reclamation Facility. • Performs physical, chemical and bacteriological tests on potable water, raw water and ...

HUNDREDS OF SCIENCE/BIOTECH POSITIONS - CLS'S, MOLECULAR, FISH, CYTO HUNDREDS OF BIOTECH POSITIONS AVAILABLE NATIONWIDE MOLECULAR; CYTOGENETICS; FISH; HISTO'S, PATHOLOGIST'S, CLS'S-NATIONWIDE, ETC..... Description: WE SPECIALIZE IN RECRUITING FOR ALL POSITIONS AND JOB LEVELS WITHIN THE BIOTECH/PHARMA INDUSTRY NATIONWIDE! WE REPRESENT SEVERAL HUNDRED CLIENTS THAT HAVE THE FOLLOWING POSITIONS AVAILABLE AT THIS PRESENT TIME... PLEASE SEE BELOW LIST: JOB OPPORTUNITIES: CLINICAL LABORATORY ...

Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea Biosciences is searching for a Regulatory CMC Manager/Associate Director to join the team. The Regulatory CMC Manager/Associate Director leads the regulatory strategy for, and execution of, global CMC (chemistry, manufacturing and controls) activities leading to ...

Allied Search Partners is looking for a qualified Molecular Genetic Technologist (Licensed CLS) candidate for a state of the art facility in the Oceanside, CA area. This position is full time permanent. Know someone for this position? We offer a $$ bonus if we place your referral in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Position: Molecular Technologist (Must be a licensed CLS) Schedule: ...

2013…..NOW HIRING….GMP QA Associate…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking an Associate Director, Analytical Sciences to join its’ dynamic team. The successful candidate will assure cGMP compliance with applicable regulatory requirements including audits and ...

2013…..NOW HIRING….Biostatistics Consultant…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking an Associate Director, Analytical Sciences to join its’ dynamic team. The Biostatistics Consultant is responsible for providing input to statistical analysis plans, and executing on ...

- The Manufacturing associate will be responsible for supporting manufacturing operations by working as an operator in all aspects of plasmid DNA manufacturing, including fermentation, lysis, and chromatographic processes and applying knowledge to troubleshoot problems as well as improve manufacturing procedures. - The Manufacturing Associate will work to execute and troubleshoot equipment during Manufacturing runs. - In addition, the Manufacturing Associate will assist the Facilities department ...

Are you a self-starter that thrives in team environments? Do you enjoy analyzing data for process experiments? Are you able to prioritize multiple projects and tasks to accomplish goals on time? Is this the type of challenge you are looking for in your career? Our client is hiring! Our client is growing its Bioprocess Development team and we are seeking a hardworking, team member to be part of our bioprocess development group working on the fermentation and downstream recovery of recombinant ...

Our client is a pioneer and recognized leader in the development and commercialization of high-performance enzymes for use in industrial processes. Are you a self-starter that thrives in team environments? Do you enjoy analyzing data for process experiments? Are you able to prioritize multiple projects and tasks to accomplish goals on time? Is this the type of challenge you are looking for in your career? Our client is hiring! Our client is growing its Bioprocess Development team and we are ...

Essential Duties & Responsibilities: - Maintains safe, organized and clean work environment. - Performs analytical testing on designated laboratory samples. - Performs chemical and physical testing on raw materials, in-process and finished products as assigned. - Operates and maintains laboratory instruments and equipment. - Performs sample log-in of receipts. Initiates the shipment of samples and tracking documents for outside contract laboratory tests. - Performs administrative tasks ...

Our client assists customers in rapidly developing, manufacturing and commercializing point of care lateral flow, flow through and ELISA assays for any market segment. Our client develops products for markets as broad as clinical diagnostics, veterinary diagnostics, food science, and microbiology and operates under design controls and GMP as required. They are seeking a Research Associate who will be responsible for research and development of products from feasibility through clinical trials and ...

Looking for a qualified SAS Programmer (home based) Requirements include but are not limited to the following: BA/BS degree in computer science, statistics, biostatistics, mathematics or related field. MA/MS degree is desirable  3-5 years of programming and clinical research or related experience Must have database management, SAS or PL/SQL programming experience Or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills ...