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Green Key Resources is currently seeking an experienced Clinical Data Manager for an immediate 12-month renewable contract. Summary:  • Manages and supports team of Data Management professionals to efficiently deliver Data Management deliverables per corporate timeline.  • Manages services providers to ensure the quality and timelines are met.  • Manages and supports staff dedicated to the implementation of the Data Management activities from study start-up to study close-out.  • Liaise with the ...

  Overview: ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries.  We offer the excitement of a consistently evolving career.  Our team is continually learning and working on new and exciting projects in a variety of regions.  We look for people who excel in their technical area of expertise, believe in our values of Experience, Integrity and Commitment and ...

  Overview: ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries.  We offer the excitement of a consistently evolving career.  Our team is continually learning and working on new and exciting projects in a variety of regions.  We look for people who excel in their technical area of expertise, believe in our values of Experience, Integrity and Commitment and ...

Qtech-Sol Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed by Clinical Research Associates and Clinical Research Monitor.   Internship includes prior training, which follows real time experience and exercise learning pattern. Training is required and may take 1.5 months to complete. Internship takes approximately 2 months depending on project needs. The students will be selected and toward ONE of the career pathways for learning. ...

Qtech-Sol Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed as Drug Safety Associates.   Before the internship the professional training is required, which provides real time experience and exercise learning pattern.   Educational Qualifications: Bachelor Degree or Higher in Life Science             Preferred degree in: Anatomy, Biochemistry, Biotechnology, Biology, Biomedical             Science, Biomedical Engineering, Chemistry, ...

We are seeking a highly motivated, enthusiastic, an independent Research Associate/Senior Research Associate to join the Clinical Pharmacology Group in the Department of Development Sciences.  Responsibilities:  The candidate will provide technical support for the pharmacokinetic and pharmacodynamics assessment of drug candidates and marketed products.  The overall scope and focus of this position is to support pharmacokinetic analyses, which seek to optimize dose regimens and strategies to ...

Title: Clinical Trial Manager II Company: Biotechnology Company Location: South San Francisco, CA Status: Full-time consulting engagement, 40 hrs/week Length: Long-term assignment: Initial term 12 months Experience the pride and satisfaction of working for one of the top Biotech Companies. Contribute to the use of human genetic information to discover, commercialize and manufacture biotherapeutics. With multiple products on the market and exciting projects in the pipeline this biotech company ...

Principal Duties and Responsibilities: 1.     Plan, coordinate and produce statistical plans for PDL clinical programs throughout the life cycle of the responsible compounds. 2.     Apply statistical expertise to ensure optimal clinical trial designs and statistical analysis methods. 3.     Help devise data capture methods (case report forms or other) for pertinent clinical programs. 4.     Create statistical analysis plan and perform analyses according to established program standard for responsible ...

 Manufacturing Technician III, Bulk Fill and Label Center The Manufacturing Technician III performs fill operation of 24+ antigens and 7+ peptides, including preparation activities such as material cleaning, autoclaving, depyrogenation, visual inspection, label issuance and reconciliation, label application and packaging. The Technician III is expected to perform operations under cGMP/ISO/FDA guidelines, follow valid procedures and documentation and work with other Bulk Fill-Label Center team ...

Manufacturing Associate III, Bulk Fill and Label Center The Bulk Fill-Label Center Associate III performs fill operation of 24+ antigens and 7+ peptides, including preparation activities such as material cleaning, autoclaving, depyrogenation, visual inspection, label issuance and reconciliation, label application and packaging. The Associate III is expected to perform operations under cGMP/ISO/FDA guidelines, follow valid procedures and documentation and work with other Bulk Fill-Label Center team ...