Job Description



8:00 pm - 8:00 am - Thursday - Wednesday

7 nights on 7 nights off

Comprehensive benefits package including PTO/ Vacation

Night Shift Team consists of two pharmacists and two technicians

Requires good teamwork and leadership skills



The Clinical Pharmacist provides pharmaceutical care to patients. Compound and dispense medications and other pharmaceuticals in accordance with federal, state and local regulations and hospital policy. Serve as a resource to other healthcare professionals including pharmacy students and residents. Consult with nursing, medical staff and patients regarding medications, orders, drug and pharmaceutical detail, patient reactions, errors and complaints and/or the patients' caregivers. Includes inpatient acute, outpatient, etc pediatrics to geriatrics.

Benefits
Health, Dental, Vision
PTO - vacation cas-in program available
Pension
Reitrement Plan - strong program
Long Term and Short Term Disabillity
Life Insurance
Flexible Spending Accounts
Cost saving insurance options for car and home owners insurance
On site Child Care
Educational Assistance Program with available scholarships

We are offering a strong compensation package with shift differential, relocation allowance, plus sign on bonus and benefits.

To apply in confidence, email your resume for consideration.




Job Requirements


California Licensed Pharmacist
Hospital Pharmacy Experience



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Description
 
Pharmacy Manager at the City Market pharmacy in Cortez, Colorado.  As the Pharmacy Manager, you will be expected to provide outstanding customer service which will include assisting our patients in proper selection of OTC items as well as accurately dispensing of prescription medications and providing counseling and answering any questions the patient may have. Supervision of day to day pharmacy operations and supervising the pharmacy staff is also the responsibility of the Pharmacy Manager. Physician interaction on behalf of the patient is also necessary.

Description
 
Full-time Staff Pharmacist at King Soopers pharmacy in Colorado Springs, CO.  You will be expected to provide outstanding customer service which will include assisting our patients in proper selection of OTC items as well as accurately dispensing of prescription medications and providing counseling and answering any questions the patient may have.  Working well with all pharmacy employees is also expected, as a team environment is mandatory to serving our customers in a timely and efficient manner.

Full-time Staff Pharmacist at City Market pharmacy in Alamosa, CO.  You will be expected to provide outstanding customer service which will include assisting our patients in proper selection of OTC items as well as accurately dispensing of prescription medications and providing counseling and answering any questions the patient may have.  Working well with all pharmacy employees is also expected, as a team environment is mandatory to serving our customers in a timely and efficient manner.

Administer high availability, reliable and effective Intranet portal integrations and utilities to support communications, content management, information delivery and workflow needs. Administer existing internet websites and portals by providing various support functions to the users.

Description
 
Full-time Staff Pharmacist at King Soopers pharmacy in Colorado Springs, CO.  You will be expected to provide outstanding customer service which will include assisting our patients in proper selection of OTC items as well as accurately dispensing of prescription medications and providing counseling and answering any questions the patient may have.  Working well with all pharmacy employees is also expected, as a team environment is mandatory to serving our customers in a timely and efficient manner.

This position is open as of 12/12/2009.

Sr. Manager In-vivo Testing - Biologics/Vaccines - MD/DC

Sr. Manager In-vivo Testing - Biologics/Vaccines - MD/DCWe develop, manufacture and commercialize immune related biologics, vaccines and biotherapeutics that assist the body's immune system to prevent or treat infectious and other life threatening diseases. Our product pipeline includes anthrax vaccines and therapeutics, botulinum vaccines and therapeutics and other vaccines.Responsibilities:• Support non-clinical development of vaccines and therapeutics.• Oversee the projects' non-clinical programs that include multiple safety, immunogenicity, and efficacy studies aimed at meeting regulatory requirements for licensure of biologics. • Oversee the design, execution, and monitoring of non-clinical studies, analysis and interpretation of the data, and ensuring compliance with the regulatory requirements. • Lead a small team of scientists responsible for the daily non-clinical operations• Interact with the U.S. Government client.• Oversee the preparation of reports and management of timelines and budgets. • Ensure success of the non-clinical programs through effective interaction with both internal and external collaborators, including scientists, CRO's, project managers, regulatory and quality assurance experts, and outside consultants. • Participate in the preparation of regulatory submission documents, as well as evaluation of and response to U.S. Government RFPs, BAAs, RFIs, and RFAs in support of new and existing products. Requirements: • PhD in Microbiology, Immunology, Biochemistry, or related discipline. M.S. with relevant experience may be considered.• 12+ years of related experience, including 8+ plus years of post-doctoral experience. • Experience in non-clinical development of vaccines and other biologics, particularly in the design and execution of animal studies. • Experience in preclinical toxicological evaluation of drugs and biologics. • Supervisory experience, strong organizational, interpersonal, and project management skills, as well as excellent verbal and written communication skills, are essential.• Knowledge of Earned Value Management System, project management training, and understanding of the U.S. Government contract requirements are a plus. • Strong familiarity with GLP guidelines and requirements for demonstration of efficacy using the FDA “Animal Rule.”Required SkillsIn-vivo, Non-clinical Development, Vaccines Biologics, Preclinical Toxicology, GLP Regulations, Regulatory Documents, Animal Studies
If you are a good fit for the Sr. Manager In-vivo Testing - Biologics/Vaccines - DC/MD position, and have a background that includes:In-vivo, Non-clinical Development, Vaccines Biologics, Preclinical Toxicology, GLP Regulations, Regulatory Documents, Animal Studies and you are interested in working the following job types:Pharmaceutical, Healthcare, BiotechWithin the following industries:Biotechnology, Chemical, PharmaceuticalOur privacy policy: Your resume and information will be kept completely confidential.Looking forward to receiving your resume through our website and going over the job in more detail with you!

Director of Medical Affairs
 
·        Guides Medical and Scientific Affairs team in support of the US Sales and Marketing organizations.
·        Acts as medical consultant on pre-marketing and post-approval issues for specific products in the US product portfolio.
·        Responsible for design and implementation of clinical projects for late stage investigational and marketed products, and dissemination of product-related information to scientific/medical community. 
·        Assures high quality of all external and internal scientific communications on company products and therapeutic areas served, through oversight of Medical Information function. 
 
Reports to: Sr Director Medical Affairs
Direct Reports:
·        3 Medical and Scientific Affairs managers  (dotted line to one or more)
·        Medical Information Specialist
·        Medical editor (includes Promotional Review Committee activity)
 
1. Provides support to US marketing and sales by overseeing all activities of Medical and Scientific Affairs function. Contributes to strategic planning and execution of sales and marketing initiatives across assigned therapeutic areas.
 
2. Oversees strategy for the development of Phase IIIb/IV clinical trials, including interfacing with community though leaders, protocol design and evaluations, in specific therapeutic areas assigned.   Drives projects to completion within budget and on time, and resolves issues within a working group when necessary.  Manages vendors of clinical services.
 
3. Interacts and organizes communication with internal and external bodies, including FDA - CBER, consultants to business unit, Clinical- Commercial (Clin-Com) Review Committee, CROs, on all aspects of company products. Actively drives publication strategy in assigned therapeutic areas to assure timely scientific publications in support of products and disease states.
 
4. Supports Commercial Operations by participating in creation and implementation of product initiatives for current products and analysis of potential new products and line extensions.  Participates in launch planning for new products and new indications of existing products.
 
5. Advances the reputation of company by contributing to the body of medical and scientific knowledge, directly or indirectly; through Medical Education initiatives; through contributions to peer-reviewed publications; and by developing strong relationships with key physicians in assigned therapeutic areas.
 
6. Supports sales trainers in the preparation of written and oral educational materials on relevant topics, on an appropriate scientific level, to be given internally to the sales and marketing departments.
 
7. Functions as strong scientific and medical expert in assigned therapeutic areas, as a resource to customers internally and externally.  Maintains and actively renews medical, scientific and regulatory knowledge by staying current on medical as well as industry research and trends. Communicates to the internal team on product information, including safety, indicated uses and ongoing research.  Functions as a resource for scientific information among constituents externally. 
 
8. Facilitate scientific/medical exchange of information internally for the Medical Information function; and externally deliver emerging scientific and clinical advances through symposia and other medical educational venues, as well as contributing to the scientific literature through abstracts and manuscripts.
Position Qualifications and Experience Requirements: Provide hiring requirements for the specified position, including educational, experiential, and competency requirements necessary for the position.
 

Full-time Staff Pharmacist in Garden City, Kansas.  Please only apply for this location once.  
 
You will be expected to provide outstanding customer service which will include assisting our patients in proper selection of OTC items as well as accurately dispensing of prescription medications and providing counseling and answering any questions the patient may have.  Working well with all pharmacy employees is also expected, as a team environment is mandatory to serving our customers in a timely and efficient manner.  You must have a valid Kansas pharmacist license!

Our Client is currently looking for a GMP Quality Assurance Manager/Associate Director for their NY location.
 
Job Scope
The GMP QA Manager/Associate Director manages and coordinates cGMP regulated QA activities. Scope of cGMP oversight is from early stage development through commercial product. Responsible for independently performing domestic and international audits/inspections that ensure compliance with the FDA and other worldwide health authority regulations/guidelines, site SOPs, protocols, and industry standards, as applicable. This includes applying developed skills to assure management that the facilities and buildings, equipment, personnel, organization, methods, procedures, records, reports, and/or controls are in conformance with applicable regulations. Applies developed skills to assure management clinical studies are conducted in accordance with applicable regulations. Provides recommendations for corrective action and tracks corrective action commitments until closure. Will develop and oversee client's quality policies and audit plans for each study. Will work with the Executive Director, QA to align SOPs, policies and procedures with client's Quality Management System. Will act as a compliance resource to client personnel.
 
Essential Responsibilities:
•Independently plans and conducts cGMP audits of manufacturing activities to assess compliance with as well as with company SOPs. Performs batch release activities for products manufactured by third parties.
•Audit and evaluate all third parties, as appropriate, to assess capabilities and compliance with all regulations.
•Work with the Head of QA to assure alignment and compliance with client's Quality Management System, support assessment of compliance and define metrics to determine performance objectives.
•Work with Technical Operations staff to identify, evaluate, and recommend solutions to issues identified in the performance of cGMP audits.
•Prepare clear and concise written reports of audit observations, including an assessment of compliance. Assess adequacy of action plan. Conduct follow up activities as needed to monitor corrective actions.
•Manage all Quality Assurance vendors contracted to perform any functions in support of the cGMP QA.
•Assist with cGMP training internally and externally of investigators and vendors.
•Participate in outside meetings and working groups, assist with assigned projects.
•Maintain professional expertise and knowledge of local and international regulations.
•May participate in special projects, as needed.