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company:(integrated resources inc)
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To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Maintains and coordinates the administrative aspects of lntegra's Clinical Affairs dept. including clinical studies..
Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing a Core Dossier for Module 3 and preparing Module 3 documents to support..
Leading medical center seeks a Senior Pharmacist Supervisor. The duties and essential job functions of Senior Pharmacist Supervisors lies in the complexity of the unit or program managed. As Senior..
Job Description: GMP experience required Pharma experience highly preferred Bioprocessing experience in a cGMP environment, knowledge of Clean and Steam in Place Systems, perform facility cleanings, collecting WFI and Clean..
Director, Global Marketing – Multiple Sclerosis Franchise 6 month contract The Director will be a key member of the global multiple sclerosis (MS) franchise team. They will have an extraordinary..
Effectively and efficiently interact with internal, clinical site and vendor personnel.Have the interest and ability to expand knowledge of clinical trial management procedures and regulatory submission requirements.Learn health care authority..
Job Qualifications: Education o High School diploma or equivalent. Experience o Minimum 2 years of experience in a retail pharmacy and strong clinical drug therapy knowledge. o Call Center experience..
Summary: Under close supervision, performs routine lab supporting in glassware cleaning, dissolution bath cleaning, dissolution media preparation, disposition of expired chemicals and reagents, handling lab wastes. Essential Job Functions: This..
Authors annual product quality review (APQR) report in compliance with FDA and internationalhealth agency requirements.Coordinates data and information collection for APQR.Supports investigations by working directly with operating entities and internal..
One of the region's leading medical centers seeks a Director of Pharmacy to oversee and manage overall department operations and assure that necessary Client and supplies are available to provide..
It is the operator's responsibility to ensure that the equipments used for e.g. Mechanical Sifter, Granulator, Fluid Bed Dryer, Fitz Mill, and blenders are clean and set up properly. It..
Primary Duties • Under the direction of the line manager, the Contract R&D Pharmaceutical Development Documentation, Training and Compliance Specialist is responsible for supporting all the documentation and training needs...
Clinical Development ScientistPrimary Role:• Responsible for providing scientific support for the company’s clinical research and product development initiatives under the direction of GCDL/GDTL• Assist in the preparation of clinical output..
Contractor Work Location: McPherson - KS Job Title: Tech Transfer Coordinator Duration: 12 Months Job Description: This role is supporting the successful execution of technical transfers to (and from) Client's..
Job Summary Job Title: Contracts and Rebates Analyst Location: Woodcliff Lake NJ USA 07677 Duration: 6 months *Description: Summary: *This position requires knowledge of contract administration including but not limited..
Job Summary Title : Analyst, Contracts and Rebates Duration : Woodcliff Lake, NJ Location : 6 months (Possible extension) Responsibilities and Duties Responsibilities Reviews and enters assigned contracts/amendments in system...
Under the guidance of the Sr. Manager, this individual will manage the Contract Manufacturing Organizations (CMOs) involved in production of drug product on-behalf of Alnylam Pharmaceuticals, to supply early stage..
Biotechnology company seeks a Microbiologist for second shift. Duties: Performs routine microbiological testing of products, raw materials, components and controlled environments according to site Standard Operating Procedures and compendial methods...
The Serologist I will be responsible for performing in-process testing all types of BioVue/Gel cassettes/cards and release testing of all types of Gel cards. This person will assure compliance with..
Works collaboratively with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and others Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for routine to basic clinical data..
TBOS Role Solid 1 year contract to start MUST HAVE: 1). pediatric oncology training background 2). 5 years industry experience pharma biotech medical OBJECTIVES: Medical Director-Pediatric Oncology leads and drives..
Job Title: Project Manager III Work Location: McPherson - KS Duration: 12 Months Job Description: Leads and directs one or more project teams. Creates, reviews, evaluates project plans and objectives...
SUMMARY The In-House CRA is based in the client's facility and will provide clinical research support and assistance in overseeing the conduct of clinical trials. RESPONSIBILITIES · Work to ensure..