Temporary, Contract, Project Club manager jobs in the Biotechnology & Pharmaceuticals industry

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TechData is hiring Biostatistician (Some positions can be telecommute), SAS Programmer/Statistical Programmer (Some can be telecommuting), Sr. Clinical Data Manager, Director of Medical Affairs, Informed Consent Specialist, Clinical Scientist, CRS (Clinical Research Scientist), Clinical trial manager/Leader for our pharmaceutical clients in Northern and Central NJ. Please see below requirements an...
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Job Title: TMF Manager Position Description This position is responsible for management of Clinical and other sections of the Trail Master Files (TMF), utilizing records management best practices and appropriate technologies. The individual will provide leadership and expertise in records management and archiving support for clinical research work. Including the completeness, safekeeping and acces...
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Job Title: Clinical Data Manager Position Description The Clinical Data Manager (CDM) is responsible for the creation, updating, maintenance and validation of clinical study databases and for the provision of computerized reports of these data. The CDM is a key member of the clinical project team and will prioritize work in line with departmental and organizational management decisions. The respon...
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Experis - Alameda, CA, 94501 (14 days ago)
Experis is seeking a Client Project Manager in Alameda, California. The Project Manager will work on extremely complex problems in which analysis of situations or data requires an evaluation of intangible variables. Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results. Manages, designs, implements, and monitors multi or singlesite clinical ...
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Job Number: 411892 Clinical Data Manager Clinical Data Manager: Job Description: Working under the direction of a senior staff member, will fully manage assigned studies during conduct to database lock. Studies are outsourced to CRO and therefore this position requires the management of CRO deliverables in accordance with timelines and internal team expectations. It involves the accurate and timel...
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Hudson, a division of Hudson Highland Group, Inc. (NASDAQ: HHGP), a $1.2 billion global company, is one of the world's leading professional staffing, outsourcing and employment lifecycle solution providers. We are looking a Junior Project Manager for a 12+ month contract for our client Thousand Oaks, CA. Job Description: This position is for a junior to intermediate project manager who will be res...
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Job Title: Global Clinical Study Manager Position Description Oversee Phase IV and PMS studies to support multiple brands in CV-Met, Immuno, Virology and Neuroscience. Position Responsibilities Demonstrates a strong operational understanding of conducting clinical trials. In conjunction with Medical Strategy and Field Medical Science (FMS) executes or oversees outsourced Phase IV and Post Marketin...
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Job Title: Regulatory Affairs Manager Position Description An individual in this role is expected to coordinate all aspects of CMC regulatory submissions relevant to their assigned projects. An individual in this role will serve as the regulatory CMC representative on matrix teams, as appropriate. Position Responsibilities Monitor changes to development plans and work with supervisor to design glo...
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Job Title: Clinical Data Manager Position Description The Clinical Data Manager (CDM) is responsible for the creation, updating, maintenance and validation of clinical study databases and for the provision of computerized reports of these data. The CDM is a key member of the clinical project team and will prioritize work in line with departmental and organizational management decisions. The respon...
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Job Title: Quality Project Manager Position Description Manage and support knowledge management, metrics reporting, and continuous improvement projects in the areas of quality and compliance. Position Responsibilities Improve and maintain the Quality Operations Community intranet site (SharePoint) Research current industry issues (e.g., Warning Letters, FDA organizational changes, new regulations)...
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Job Title: Regulatory Affairs Manager Position Description Serves as a liaison between the company and regulatory agencies for all assigned projects and is responsible for day to day regulatory support. Expected to provide guidance within Regulatory Affairs and to data generating departments to ensure timely filing and approval/maintenance of assigned programs. Position Responsibilities Responsibl...
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Experis - Raleigh, NC (7 days ago)
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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FEI Company is seeking a Recruiter to join our team. This is a long term contract at our global headquarters in Hillsboro, Oregon. This person will own the recruitment process for assigned requisitions. This includes consulting with the hiring manager, sourcing candidates, screening candidates, scheduling candidate phone screens and interviews, updating the applicant tracking system, consulting wi...
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To participate in the research and analysis of system application needs and problems for users; to provide assistance, advice, problem solving, and technical information to customers regarding the use of software applications; and act as liaison with customers regarding the status of their requests. Provides technology and application support to IS clients, assesses business and technical requirem...
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Job Title: Clinical Research Associate Position Description: As primary liaison between Company and the investigator, performs on-site monitoring visits and associated planning and follow-up activities; works with the Manager, Clinical Operations, Clinical Research Manager and other members of the clinical project team in the planning and execution of clinical trials Position Responsibilities Part...
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TechData is hiring SAS/Stat Programmers (Some can be telecommuting), Biostatistician (Can telecommute), and Architect in Gaithersburg, MD. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitive pay rate and benefits. TechData is the leading supplier in the pharmaceutical consulting industry. Sr. SAS Pr...
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Company Confidential- Freemansburg, PA, 18017 (7 days ago)
Chemical Operators Third Largest Manufacturer of Inhalation Anesthetics Globally has 5 positions for Chemical Production Operators. 3 positions are 12 hour nights and 2 positions are 12 hour days. Only two of the positions on 12 hour nights are temp to hire. The other positions are long term temporary only. Job Summary: Synthesizes and purifies inhalation anesthetic agents through the operation an...
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We have an opening for a contract QC Analyst for a well established Pharmaceutical company in the East Bay. The QC Analyst reports to Lab supervisor or manager. Conducts routine and non-routine analyses of raw materials, formulations, in-process and finished products according to standard operating procedures. Performs analyses for stability samples. Analyzes data and compiles data for documentati...
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Reporting to the District Manager, the Cardiovascular Nurse Specialist is implementing the clients marketing plan and product education plan to hospitals and pharmacies by using their professional expertise and clinical training. Essential Functions: Deliver proficient and clinically-supported presentations to a defined list of approved hospitals Utilize only approved marketing and educational mat...
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Reporting to the District Manager, the Cardiovascular Nurse Specialist is implementing the clients marketing plan and product education plan to hospitals and pharmacies by using their professional expertise and clinical training. Essential Functions: Deliver proficient and clinically-supported presentations to a defined list of approved hospitals Utilize only approved marketing and educational mat...
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Company Confidential- Birmingham, AL, 35201 (28 days ago)
Reporting to the District Manager, the Cardiovascular Nurse Specialist is implementing the clients marketing plan and product education plan to hospitals and pharmacies by using their professional expertise and clinical training. Essential Functions: Deliver proficient and clinically-supported presentations to a defined list of approved hospitals Utilize only approved marketing and educational mat...
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Company Confidential- Charleston, SC, 29401 (28 days ago)
Reporting to the District Manager, the Cardiovascular Nurse Specialist is implementing the clients marketing plan and product education plan to hospitals and pharmacies by using their professional expertise and clinical training. Essential Functions: Deliver proficient and clinically-supported presentations to a defined list of approved hospitals Utilize only approved marketing and educational mat...
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Hays US - Richmond, VA, 23235 (29 days ago)
SAS Programmer A large and globally renowned Pharmaceutical company are currently recruiting for a SAS programmer based in Richmond, Virginia. This is a long term contract expected to last until February 2014, paying a generous hourly rate plus overtime. This position is interviewing immediately and can start as soon as possible. The successful candidate will have 3 - 5 years of SAS Programming ex...
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· Reviews clinical data/information and oversees data correction. · Work with the Clinical Study Manager to satisfy applicable regulatory standards. · Evaluates and analyzes clinical data. · Designs experimental protocols and patient record forms. · Review and triaging clinical trial deaths and adverse events (AEs) including serious adverse events (SAEs). · Conduct Case Management in the Clinical ...
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