a member of the iHireJobNetwork  Ad Agencies  Affiliates  Site Map 
Why iHireHealthCareAdministration?



Healthcare Area Administrator Jobs

Search all 1,323 Health Care Administration Jobs for Healthcare Area Administrator Jobs


Job Title: Marketing Director/Admissions
Company: Private
Location: Ennis, TX

Description:
Marketing Director/Admissions Coordinator needed for a 114 bed facility. The ideal candidate will have a minimum of 2 years experience and will be responsible for marketing the facility within the local community and surrounding area with a special emphasis on the local medical community. Marketing efforts will also include a 1.5 million dollar rehab wing expansion project scheduled for completion in the Spring of 2010.




Job Title: Associate Director of Medical Affairs
Company: Qiagen
Location: Germantown, MD

Description:
Associate Director of Medical Affairs   Responsibilities The Associate Director of Medical Affairs will provide essential support to the North American and global business organizations. These organizations include QIAGEN Sales and Marketing, Research and Development, Business Development, Regulatory and Legal Departments, and Corporate Communications. Product and basic medical training for the sales force and other groups in the organization are part of the job spectrum. This position will also be a strategic corporate interface with professional provider communities, societies, and events. Major responsibilities include: Participation in the design and development of current and evolving HPV testing studies Facilitation of scientific and clinical relationships with key opinion leaders guidance and review of promotional and educational materials for accuracy and completeness Coordination of corporate consultant and advisory board meetings; to include the establishment and maintenance of a KOL (Key opinion Leader) board of 15-20 physicians Advising QIAGEN leadership on clinical affairs, activities, and relations assisting the commercial team in development and communication of consistent global and regional brand messaging Providing strategic risk management consultation, program coordination and support Job Requirements Position requirements, qualifications, and experiences: M.D. degree, Board Certified or Board Eligible in Designated Specialty (preferred) Or PhD in Science Minimum three years clinical or clinical research experience Minimum two years experience in the pharmaceutical industry Excellent communication and presentation skills, strong interpersonal skills. Strong clinical research/medical affairs background and excellent problem solving abilities Demonstrated abilities to work effectively in a team matrix environment Ability to interpret and evaluate clinical data to bridge marketing and science needs Demonstrated leadership skills and ability to effectively manage projects and timelines. Knowledge of pharmaceutical/diagnostic clinical development and ability to effectively apply technical principles, theories, and concepts to a corporate environment Knowledge of FDA, other regulatory agency and professional requirements, regulations and guidances. Ability to work independently on all aspects of assigned projects Excellent organizational skills Excellent communication and presentation skills, strong interpersonal skills Demonstrate abilities to work effectively in a team matrix environment Leadership skills and ability to effectively manage projects and timelines




Job Title: DIRECTOR MEDICAL EDUCATION & PUBLICATIONS - Bridgewater, NJ
Company: Enzon Pharmaceutical
Location: Bridgewater, NJ

Description:
Enzon Pharmaceuticals is a biopharmaceutical company dedicated to the discovery, development and commercialization of therapeutics to treat life-threatening diseases. The Company has developed or acquired a number of marketed products, including PEG-INTRON®, marketed by Schering-Plough, and ABELCET®, ONCASPAR®, ADAGEN®, and DEPOCYT®, which are all marketed in North America by Enzon’s hospital sales force.  Enzon’s science- focused strategy includes an extensive drug development program that leverages the Company’s macromolecular engineering technology platforms, including PEG modification and single-chain antibody (SCA®) technologies.  Internal research and development efforts are complemented by strategic transactions that provide access to additional products, projects, and technologies.  Enzon has several drug candidates in various stages of development, independently and with partners. Enzon Pharmaceuticals corporate headquarters is located in Bridgewater, NJ.  This position will have oversight of the Educational Grant Website and Review committee and will be accountable for Enzon publications and medical education planning, processing, developing and executing. Other responsibilities include assisting in the review of all medical content for publication planning, speaker development, CME activities, internal training and promotional materials, and opinion leader development and management. The Director will be a member of all brand teams providing input on Medical Affairs support of brand strategy. You will interact internally with Marketing, Finance, Market Research, Regulatory, Legal, R&D and all departments within Medical Affairs. External relationships will include medical communication agencies, national thought leaders in the areas of oncology, infectious disease, transplant, immunology and clinical pharmacy. Requirements include an Advanced Scientific Degree; PharmD preferred or healthcare degree with appropriate experience considered; MBA a plus. Minimum of 8 years prior Pharmaceutical Medical Affairs experience and/or previous Medical Marketing experience required with an emphasis on Medical education and Publication Planning and strong clinical orientation with a minimum of 3 years clinical experience also required. Strong knowledge of FDA regulations, OIG and ACCME guidelines; strong analytical and evaluative skills with the ability to interpret clinical studies and data; and ability to translate/facilitate and communicate complex science and clinical concepts to different medical audiences are musts. Ability to travel to major medical conferences and advisory boards also required. We are prepared to offer you a competitive compensation and benefits package. Please send resume with cover letter, including salary history to:ENZON Pharmaceuticals, Inc.Sean Fitzmorris, Recruitment Manager685 Rt. 202/206Bridgewater, NJ 08807E-mail: Register to View Enzon Pharmaceuticals is a Tobacco Free Company




Job Title: Medical Director (Drug Safety)
Company: Clinical Staffing, Inc.
Location: Wayne, PA

Description:
Medical Director - Drug Safety (Must be MD) About Us Clinical Staffing Inc. is a national Pharmaceutical recruiting firm that focuses on Clinical Personnel such as CRA's,Data Management, Regulatory Affairs and Quality Assurance. Our clients are Pharmaceutical, Biotech and CRO companies. We cover all over the US with majority of the jobs located in NJ,PA, California and Mass. areas. We work with small to Fortune 500 companies Medical Director/Drug Safety Physician Under the oversight of the Medical Surveillance and Risk Management Vice President and in collaboration with key colleagues in PV&RM, the PV&RM Director is responsible for ensuring appropriate medical safety assessments and surveillance, compliant regulatory authority reporting, development and implementation of risk management strategies, and communication of safety information for assigned products, globally. • Oversee investigational and postmarketing regulatory reporting and pharmacovigilance activities for assigned products • Lead the development and execution of risk management strategies and author internal risk management plans and risk management/pharmacovigilance plans for submission to global health authorities, as required• Medically review individual case safety reports from post-marketing surveillance, from interventional and observational clinical trials, and from compassionate/named patient use.• Oversee, prepare and review scheduled Periodic/Annual Reports (FDA) and Periodic Safety Update Reports (FDA and Global Regulatory Agencies)• Oversee, prepare and review responses to ad hoc regulatory queries• Assist the Medical Surveillance and Risk Management VP in developing and maintaining state-of-the-art pharmacovigilance processes and procedures within R&D, and as part of the Global PV & RM organization• Lead pharmacovigilance activities as a member of drug development project teams; co-lead Safety Review Teams • Lead safety-labeling activities for assigned products.• Support the Qualified Person for Pharmacovigilance in the EEA relative to issues related to assigned products Requirements • Medical Degree required• Post-graduate training in a clinical discipline subspecialty preferred, hands-on clinical practice experience desirable.• Will generally have at least 3 years of pharmaceutical industry experience, within a relevant department (e.g. clinical development, drug safety, medical affairs).• Strong post-marketing and investigational event and aggregate assessment/review/ documentation skills; must have experience is writing/oversight of Annual Reports, PSURs, Type II Variations.• Must have a strong working knowledge of ICH guidelines, FDA & EMEA Regulations and must be experienced in safety reviews of IBs, protocols, final clinical study reports, and summaries of safety.• Experience in communicating with the EMEA and/or FDA or other recognised local Competent Authorities.• Global drug safety experience preferred.• Ability to read, analyse and interpret scientific and technical journals.• Must have very strong English language writing skills and mature verbal communication and presentation skills.• Working knowledge of MedDRA coding and case series retrieval strategies.• Experience using a large-scale electronic data storage and retrieval system.• Requires strong attention to detail in composing and/or proofing materials, establishing priorities, scheduling and meeting deadlines.• Ability to work in a fast paced environment with demonstrated ability to simultaneously manage multiple competing tasks and demands.• Ability to work independently, take initiative and complete tasks to deadlines.• Proven ability to independently resolve problems and conflicts.• Excellent interpersonal, analytical, managerial, and organizational skills.• Demonstrated ability to motivate, mentor, influence and collaborate with others in a complex global organizational matrix.• Ability to empathise with and support staff working in other national environments. Please send resumes to Register to View or Call Jesse Gill Recruiter Clinical Staffing Inc. Register to View Register to View an> tr>




Job Title: Director of Medical Records
Company: Life Care Centers of America
Location: Phoenix, AZ

Description:
At Life Care Centers of America, we appreciate your desire to care for others and appreciate your strengths as a professional. Our focus is mission-minded with the intention of giving only top-quality care to those in our facilities. We strive to excel in the healthcare industry by constantly moving with the age of technology and the new ways of business. As a community, we appreciate who you are. We thrive from growing together and forming relationships that are irreplaceable.We also understand that you want to succeed not only as a person, but as a professional. This is why we offer many professional growth opportunities for you to advance your career.The HEALTH INFORMATION MANAGEMENT (HIM) DIRECTOR maintains the residents’ clinical records, including coding, auditing, and providing pertinent staff education regarding recordkeeping procedures in accordance with state, federal, and LCCA policies and procedures. Also serves as the designated Privacy Official for the facility. At LCC Paradise Valley, our competitive benefits package will help you feel secure in your new position: medical and dental coverage 401(k) paid vacation and holidaysPlease contact:Dee Dee Ramon, E Register to View -phon Register to View -faxSkills/ Requirements• Must possess a college degree or an equivalent combination of education and experience• Must be credentialed as a Registered Health Information Administrator (RHIA) or a Registered Health Information Technician (RHIT) or have a degree in a health related field with extensive training and demonstrated competence in the HIM field• Must have training in long-term care health information management




Job Title: Associate Director - Medical Science Liaison - Endocrinology
Company: SciencesCrossing
Location: Cambridge, MA

Description:
Associate Director - Medical Science Liaison - EndocrinologyResponsibilities: Direct activities of assigned medical liaison team - ensure clear objective setting and performance management in place. Serve in the Medical Liaison role to assigned national key opinion leaders. Ensures the cascade and acceptance of core messages to key opinion leaders. Participate in delivering disease state and product training within team. Oversee the preparation and delivery of accurate, impactful presentations that support core therapeutic area messages to key opinion leaders (advisory boards, educational lectures, speaker training). Assure all follow company and regulatory requirements associated with their roles and responsibilities. Other related duties as assigned.Requirement: An Advanced science degree with therapeutic area expertise is strongly preferred. 3 years of pharmaceutical industry experience 1 of which were in either Clinical Development or Medical Services/Affairs position. Previous successful management experience of high level professionals is strongly preferred. Good understanding of Good Clinical Practices and drug development guidelines. Experience in clinical study protocol design, review and implementation. Strong analytic capabilities and ability to work independently.For further information, please visit us online at http://www.sciencescrossing.com Please send your resume to SciencesCrossing at Register to View Apply Now There will be charge of $29.95 per month (or a lower monthly rate based on agreement length) after your 7 day FREE Trial to use our service.




Job Title: Physician – Medical Director – Medical Informatics
Company: MRINetwork
Location: San Francisco, CA

Description:
Physician – Medical Director – Medical Informatics We have a strong opportunity for someone interested in a Medical Director – Clinical Informatics position for a subsidiary of a large respected and affluent healthcare system in the western region. Position is located in the greater San Francisco bay area with the systems corporate establishment. This position reports to the Chief Medical Officer and works in collaboration with the SIP Medical Director for the health system. Candidates will be physicians working in Family Practice, Internal Medicine, or Pediatrics.  This is a very important position and requires a licensed practicing physician that is highly motivated and interested in pursuing a position that will cater predominantly to the clinical informatics and healthcare delivery systems for the institution.  Successful candidate will:  Support and champion the implementation of EMR systems catering to physician integration Have working knowledge of Centricity and EPIC Works collaboratively with SIP administrative team to define strategies for the implementation and increased use of web based clinical systems Liaison for communication between the EMR steering committee and clinician users Educate clinicians and physician groups on the applications skills of the EMR system Push towards automation and use of web based tools and Assist on workflow testing for upgrades and/or new clinical programs Maintain an active clinical presence and membership in the systems independent physician group Will work approximately 60% administrative and 40% clinical in their respective specialty (Has the potential to develop into a 100% administrative position)  Successful candidate must have: A Doctor of Medicine Degree (MD), Doctor of Osteopathic Medicine (DO) with Board Certification (BC in Internal Medicine, Pediatrics or Family Practice Medicine) Current California Medical License A minimum of 5 years of clinical experience A minimum of 2 years experience working with EMR systems, preferably with Centricity products Formal training in clinical informatics The ability to communicate effectively and appropriately The ability to train and coach effectively The ability to explain and present technical information to non-technical users  We are offering a strong compensation, benefits, bonus, and relocation (if needed) structure for the qualified candidate.   Physicians coming from active practice with very little management experience, but have sufficient experience and formal training in clinical informatics are encouraged to apply Please contact or send resume to:   Jonas I. Wilber, NAM National Account Manager, Healthcare Specialist Management Recruiters Of FRESNO 5715 N. West Avenue, Suite 101Fresno, CA 93711 Tel1: Register to View x119Tel2: Register to View x119Fax: Register to View   Register to View -fresno.com www.mrinetwork.com  MRINetwork®  EXPERTS IN GLOBAL SEARCH 




Job Title: Medical Director
Company: Correct Care Solutions
Location: Washington, DC

Description:
  Are You Ready To Take The Next Step In Your Career?   Do You Want To Take Your Career In Another Direction?   Working At Correct Care Solutions May Be Just The Career For You!   Medical Director Topeka, KS     Correct Care Solutions (CCS), a leading provider of health care to correctional facilities,  is looking for professionals that are dedicated to the highest levels of patient care.     CCS allows you to concentrate on the patient and not the paperwork.  This position is for someone who is ready to take the next step in their career or someone that is wanting to take their career in a different and exciting direction.   Correctional healthcare is one of the safest, most rewarding, and professional careers in the healthcare field.   CCS currently has a part-time Medical Director position open at our Topeka Correctional Facility in Topeka, KS.    The Medical Director provides clinical oversight to the facility medical program. Supervises care given by other professional or non-professional personnel providing instructions as needed.  Reviews and countersigns therapeutic orders and corresponding progress notes of inmates seen by the physician assistant/nurse practitioner are appropriate and effective. Consults with medical specialists for advice and expertise in their respective areas.    Please apply online Register to View http://www.correctcaresolutions.com/ or e-mail CV's to [Click Here to Email Your Resumé]   CCS is an Equal Opportunity Employer Requirements Doctor of Medicine from an accredited University. Proper licensure for the state of Kansas.  Family Practice, Emergency Medicine, Internal Medicine or Public Health experience.




Job Title: Medical Director, Chronic Kidney Disease-Nephrologist
Company: Laboratory Corporation of America
Location: CHICAGO, IL

Description:
The Medical Director, Nephrologist will be the face ofthe program of Litholink to the medical and managed carecommunity. The responsibilities are asfollows:-Promoting the general medical necessity of ChronicKidney Disease testing, and in particular, the merits ofour programmatic approach to physician groups andmanaged care organizations. -Presenting data of work work at nationalsocieties, networks, and guidelinegroups. -Taking direct calls from physician customers to helpwith general questions about the management of the CKDpatient in our program. -Lead and coordinate process improvements and bestpractices in the development of the CKD program incollaboration with the Advisory Board as needed.-Providing strategic oversight of the CKDprogram. -Producing high quality peer reviewed research papers tobe published. -Serving on a pro-bono basis in a CKD teaching clinicapproximately 1/2 day or one full day per week.-Ensures compliance with required national qualitystandards regarding laboratory practices, policies, andprocedures.Required Skills:Licensed Nephrologist & License in State where the laboratory is located, and meet applicable CLIA requirements. Expert in the field of clinical management of the CKD patient. Job Code : 087093 Division/Department : Diagnostic Sciences Travel Required : 10-20%




Job Title: Medical Director
Company:
Location: Belleville, IL

Description:
- Medical Director - RN Menard Correctional Facility * PREMIUM WAGES * FULL BENEFITS including MEDICAL/DENTAL/VISION at low rates * Up to 34 PAID DAYS off in 1st year * 2 pay raises per year * Potential for Tuition Reimbursement * 401K Match When ordinary patients are just too... well, ordinary... ...it's time to join Wexford Health Sources - a privately owned and nationally recognized leader in contracted medical services for correctional facilities. Here, you'll get a chance to work in a safe environment with those who really appreciate your efforts, without the distraction of family interaction or insurance bureaucracy - simply a lot more REAL patient care. Requires current IL licensure. For more information and to apply, please fax or email resume to: Anna Vozar Staffing Consultant [Click Here to Email Your Resumé] Phone: Register to View Fax: Register to View An Equal Opportunity Employer M/F/D/V Wexford Health SOURCES INCORPORATEDSource - Belleville News Democrat Requirements Please refer to the Job Description to view the requirements for this job




iHireLLC - iHireHealthCareAdministration
iHireLLC - iHireHealthCareAdministration 1999 - 2009 iHire LLC, All Rights Reserved.
Candidate Toll Free Customer Service: 866-238-0161
Employer Toll Free Customer Service: 877-798-4854
Privacy Policy
iHireLLC - iHireHealthCareAdministration
iHireLLC - iHireHealthCareAdministration
iHireLLC - iHireHealthCareAdministration