Dear Life Sciences Professional,
DNAjobs.com is proud to feature the following jobs posted April 3 - 10 (listed in chronological order). For each position, I have listed a short description and a link for more information.
As always, I wish you tremendous success in your searching!
Jason
Clinical Application Specialist II - B
(US-Illinois) For more than a century, our client has been working to advance health care for people around the world. They have evolved into a diversified health care company that discovers, develops, manufactures and markets innovative products and services that span the continuum of care from prevention and diagnosis to treatment and cure. They provide total integrated solutions across the health care spectrum for some of the worlds most prevalent medical conditions, including AIDS, cancer and diabetes. Our client, a major pharmaceutical company in Lake County, IL is looking for a Clinical Application Specialist II - B with the following qualifications: REQUIRES 3-5 YEARS EXPERIENCE Generate tables, listings, and graphs for compound projects. Responsible for the validation and quality assurance of any output produced. Generate and review validated table, listings, and graph output meeting the needs of Clinical Projects. Prefer candidate with SAS program and clinical experience. BS Preferred. You MUST meet all of the above qualifications in order to be considered for this position.
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Image Consultant
(US-California-San Francisco) Description Adaptation of standard image processing techniques or, where necessary, development of novel techniques for analysis of DNA microarray image data. Typical projects include deblurring, dewarping, segmentation and compression of images taking advantage of the rich structure present in DNA microarry images. Work would be as part of cross-functional project team, working with hardware, firmware and other software engineers to implement and validate new methods. Requirements: -Requires a Masters degree in a numerate discipline, PhD is preferred. Prior experience in image analysis and image processing. Expert knowledge of C++. Familiarity with Matlab. Strong communciation skills is essential. Ability to work effectively as part of a multi-disciplinary team. Experience/knowledge of confocal microscopy an advantage.
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Research Technician
(US-Texas-Houston) Wonderful bright bright boss who expect hard work. Has to be familiar with variety of procedures of molecular biology, biochemistry, genetics and cell biology. Duties: microarray analysis (isolation of RNA,cDNA synthesis, hybridization, and computer analysis of data); sequence analysis and preparation of sequence data for publications, analysis ES cells by Southern hybridization and work with mice. Other duties include ordering, solution preparation and record keeping. Degree will be verified, background check also. References checked. Located in Medical Center.
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Senior Manager / Manager
(US-California) Requirements: BS in Comp Science/Engrg or equivalent 7+ years technical experience with emphasis in software engrg. and/or DBA including hands-on system analysis, design, development & maintenance. In-depth exp EXperience with MS SQL & Oracle. Good understanding of web technologies. Experiencewith application integration,data warehousing, business process management, project management tools. Must have experience in biotech /pharma industry. Experience as a manager is necessary. Experience with software development methodologies,coding standards & production controls. Responsibilities: Manage all IT related application integration & development projects. Project planning, identifying milestones, deliverables & resource requirements, & tracking activities & task execution. Provide technical direction and support to departmental Project Manager. Understands SDLC methodologies, identifying areas for improvement & participating in their refinement. Lead a team of Business Analysts, Application Developers, DBA (internal or external) prioritizing their work & deploying them as necessary to ensure work flow effectiveness.
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Research Scientist - Peptide Formulation
(India) Experience: 3-5 years of experience in HPLC and GC analysis. Should be well versed with regulatory analytical requirements including methods validation and documentation. Qualifications: The candidate should have a Ph.D. degree in Analytical Chemistry. Location: R & D Centre - Aurangabad
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Manager - Intellectual Property Rights
(India) Experience: Atleast 5 - 7 years experience in patent searches, PCT/US patent filing and giving non-infringement opinions. Working knowledge of computer and internet operations for patent search is a prerequisite. Qualifications: The candidate should be a Ph.D. in Pharmaceutics / Organic Chemistry / Biotechnology. Location: R & D Centre - Aurangabad
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Clinical Data Manager
(US-Oregon-Portland) Clinical Data Manager- $55K Job Responsibilities: Provide CDM support to client's personnel and clinical sites. Prepare and maintain key validation documents according to company standards. Create and update the DMP as needed. Develop file/format specifications, program data transfer code, QC and process data transfers. Define, run and review data validation output and resolve discrepant data. Collaborate with engineering group for development and testing of CDM software tools. Track metrics and processes, including monitoring workload, supervising day to day activities, measuring progress, identifying resourcing requirements, providing high-level support, and ensuring deliverables are met according to study contracts. Assist in implementation of department working policies. Perform defined data checks for pre-determined transfer requirements. Requirements: Education: Bachelor's Degree in Life or Social Science Experience: 3 - 5 years data management experience. Knowledge of clinical research, GCP, GCDMP and related regulatory requirements.
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Clinical Research Associate
(US-California-San Francisco) Clinical Research Associate - $45K. Description: To assure timely delivery of high quality data analysis for clinical trials. Responsibilities: Analyze data according to SOP. Load data into study specific databases. Identify and document unacceptable or questionable scans. Maintain database and reconcile discrepancies. Organize forms, hardcopies and electronic media for data tracking. Prepare and distribute study specific documents including QA manual, training materials and other study specific materials. Maintain study documentation according to SOPs. Request missing or incomplete information. Prepare and document correspondence with sites and sponsors. Certify technologists for study participation. Provide information needed to process IQC data. Provide information necessary to conduct cross-calibration. Support other Research Associates as needed. Monitor and report measures of project performance to Project Manager(s). Requirements - Education: Bachelor's Degree in Science or health related field; or three years relevant experience.
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Clinical Project Manager
(US-California-San Francisco) Clinical Project Manager - $70K. Job Duties: Lead multi-discipline project teams in delivery of clinical trial services to sponsors. Responsibilities: Lead project team of radiology, densitometry, molecular markers, data management, engineering and science. Manage study activities, direct and coordinate efforts across client's offices for the delivery of services and multiple data sets. Provide leadership for study start-up and study activities. Provide a central point of communication for study sponsor, study team and senior management. Interact with sponsor, business development and study team to ensure smooth study start-up and data flow. Provide all start-up information to departments and other study team members. This information includes, but is not limited to: Internal Study Reference (provides all relevant study information, i.e., tests performed, service schedule, investigator lists, protocol, contract, forms to be used, procedures to be followed, lines of communication for the study). Facilitate study progression by overseeing study activities, including internal and CRO/Sponsor activities.
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QA Radiological Technologist
(US-California-San Francisco) QA Radiological Technologist- $70K (specifically as an imaging QA reader and measurements specialist) position. Responsibilities: The incumbent provides expert quality assessments of medical images such as radiographs, MR scans, CT scans and ultrasound according to client's SOPs, Sponsor requirements and GCP requirements. The incumbent provides expert 3-D measurements of tumor volume for tumor response assessment and JSW measurements. Participate in reader training and validation sessions Train other readers in 3-D and JSW measurement techniques. Contribute to development of optimized and standardized 3-D measurement for each study requiring such measurements. Provide radiological training to Sponsor, clinical site and client's personnel. Contribute to radiographic procedures and quality assurance manuals and image atlases. Contribute to the development of and delivering presentations to clinical site personnel. Provide clinical site personnel help-line assistance regarding issues of radiological image acquisition techniques and quality standards.
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MRI Technologist
(US-California-San Francisco) MRI Technologist- $70K Client is looking for an MRI technologist willing to travel to perform on-site trainings for large clinical trials using MRI in neurological, oncology (DCE-MRI) and musculoskeletal disorders. Job Duties: Perform Phantom QC for site qualification and periodically during study,for every site. Provide expert quality assessments of medical images such as MR scans and CT scans. Field all technical questions from sites about MRI protocol and format/structure of data. Provide tolerances for parameter checks on data and advise on borderline cases as data is received. Upon request of repeats for phantoms or patient's exams, communicate with the sites to give them feedback on how to avoid repeat exams. Critically review documents, manuals, forms and MRI protocol. Test the MR protocols on different MR equipments. Trouble shoot any problems on incoming data with header or loading imaging data. Assist radiologists with patient QC as needed. Assist in preparation of training presentation. Provide technical assistance in conduct of remote MRI technologist teletrainings. Perform all on-site MRI technologist trainings.
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Corporate Manager - Research & Development
(India) The candidate should be Ph.D in Plant Breeding & Genetics with sound knowledge of latest plant breeding techniques and biotech tools. 10-15 years work experience in commercial plant breeding in a reputed organisation is essential. Candidate should have good communication & interpersonal skills and capable of leading a large team working at multiple locations. TRAINEES / MANAGEMENT POSITIONS Fresh B.Sc.(Ag) /M.Sc. (Ag) with good academic track record and communication skills to work in Research, Product Development, Production and Sales functions at various locations in the country. Candidates with 1-2 years work experience in the related function of seed industry will be considered for entry level mangement positions.
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