better Biotech Pharma Job in Indiana

Clinical Pharmacist Department: CHS - Pharmacy Schedule: Full Time (Benefited) Shift: Days/Evenings Hours: Job Details: DUTIES: To review and evaluate drug regimens, which include the medication profile, in order to identify issues which require pharmacy intervention or monitoring. Clinical functions include patient education, management of medical staff approved protocols, and participation in multi-disciplinary rounds. Distribution responsibilities include reviewing and interpreting physician medication

Clinical Pharmacist Department: TIHH - Pharmacy Schedule: Full Time (Benefited) Shift: Days/Evenings Hours: Job Details: DUTIES: Clinical functions include patient education, management of medical staff approved protocals, and participation in multi-disciplinary rounds. Distribution responsibilities include order review, order entry, admixing IV's and preparing unit dose medications for nursing, code blue participation, competency in core clinical functions. LICENSURE: Current IN Pharmacist licensure. ADDITIONAL

Clinical Pharmacist Department: CHE - Pharmacy Schedule: Part Time (Benefited) Shift: Days/Evenings Hours: Variable Job Details: Graduate Degree DUTIES: Clinical functions include patient education, management of medical staff approved protocals, and participation in multi-disciplinary rounds. Distribution responsibilities include order review, order entry, admixing IV's and preparing unit dose medications for nursing, code blue participation, competency in core clinical functions. LICENSURE: Current IN

Clinical Pharmacist Department: CHN - Pharmacy Schedule: Part Time (Benefited) Shift: Days/Evenings Hours: Variable Job Details: Bachelor's Degree DUTIES: Clinical functions include patient education, management of medical staff approved protocals, and participation in multi-disciplinary rounds. Distribution responsibilities include order review, order entry, admixing IV's and preparing unit dose medications for nursing, code blue participation, competency in core clinical functions. LICENSURE: Current

Clinical Staff Pharmacist Department: Pharmacy Job Code: C057-RPh (PRN) Schedule: PRN Shift: Day Hours: Weekday Availability, weekend call responsibility Job Details: Be a Part of Something Awesome! Healix is a national leader in providing high-tech pharmaceutical services in physician-office based outpatient infusion therapy settings. Qualifications: ? IV Infusion Experience ? Clinical Patient Management ? Excellent Communication Skills ? Home Infusion Background a Plus

Requires current Indiana license or eligibility for Indiana licensure as a Pharmacist Board Certification in...outcomes QUALIFICATIONS KNOWLEDGE SKILLS ABILITIES Requires current Indiana license or eligibility for...

Current State of Indiana Pharmacist license required...

KNOWLEDGE SKILLS ABILITIES Requires current State of Indiana licensure as a Registered Nurse Basic Life...

KNOWLEDGE SKILLS ABILITIES Requires current State of Indiana licensure as a Registered Nurse Basic Life...

KNOWLEDGE SKILLS ABILITIES Requires current State of Indiana licensure as a Registered Nurse Basic Life...

Manager Biotech New Product Planning Location Indiana Indianapolis Education Required MBA Job ID 50327392...

A Pharmaceutical company has an immediate opening for a Clinical Research Coordinator in Indianapolis Indiana...

Indiana is the preferred location...Job Category Clinical Affairs Location United States Indiana United States Missouri United States Michigan United...

A CRO has an immediate need for a Home-Based Regional CRA to cover sites in the Midwest. Regional Clinical Research Associates are involved in all aspects of clinical trials management, including initiating, investigating and monitoring of clinical studies. Regional CRAs are home-based and travel within their region. Major job duties and responsibilities: - Monitor clinical trial sites from pre-study through closeout. - Travel regionally between 60-80%. - Ensure site compliance. - Manage protocols. - Work with

accredited School of Pharmacy and a Current Indiana license as a pharmacist...

Job Classification: Direct Hire Description: A CRO has an immediate need for a Home-Based Regional CRA to cover sites in the Midwest. Regional Clinical Research Associates are involved in all aspects of clinical trials management, including initiating, investigating and monitoring of clinical studies. Regional CRAs are home-based and travel within their region. Major job duties and responsibilities: - Monitor clinical trial sites from pre-study through closeout. - Travel regionally between 60-80%. - Ensure

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic Assistant Clinical Data Manager/Data Team Lead to join our team!

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic Assistant Clinical Data Manager/Data Team Lead to join our team!

Clinical Research Associate / CRA / Sr CRA Description The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA

Concentrics Research is a unique CRO specializing in late-stage (Phase II IV) research. With more than 20 years of expertise in clinical and regulated healthcare marketing research, we create and execute custom research to meet our clients needs. We work with some of the leading pharmaceutical, biotechnology, nutritional/dietary supplement and medical device companies nationwide. At Concentrics, we re centered around our clients AND our employees, with concentric circles of knowledge, experience, service

Central Indiana Cancer Centers has an exciting opportunity for a Clinical Research Coordinator in Indianapolis IN...

We were also named Indiana s only hospital to be recognized for...licensure or eligible for licensure by the Indiana State Board of Pharmacy Completion of a...

Be a Part of Something RARE and AWESOME Position: Clinical Staff Pharmacist (PRN) Highland, IN (C057) The Company As the leading authority on the management and provision of parenteral services, our program enables our clinical team to provide leading-edge treatments in an ambulatory setting. Infusion therapy, for specific disease states, is provided by collaborative care teams, which combine the skills and expertise of the physician, pharmacist, and nurse to benefit the patient. Our team approach

Cary North Carolina Eden Prairie Minnesota Indianapolis Indiana Lexington Kentucky Lenexa Kansas San Diego California...

At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance s impressive history of company stability and growth. We ve achieved these results by fostering a work environment that encourages, develops and leverages our team s capabilities. Covance s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! Data Managers

UnitedHealth Group is an innovative leader in the health and well-being industry, serving more than 55 million Americans. Through our family of companies, we contribute outstanding clinical insight with consumer-friendly services and advanced technology to help people achieve optimal health. i3 Research is a full-service, global CRO specializing in central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. We approach our work with an intense

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team in our Midwestern region. The clinical research

Qualifications - Bachelor s degree in clinical, biological or mathematical sciences, nursing degree or related field, with a minimum of 3 years experience in a clinical data management role, specifically in a CRO, pharmaceutical or biotech environment or the equivalent of education, training or experience. - Candidates must have prior work experience in a lead role, managing assigned projects on all levels, acting as the lead. - Candiate must have a thorough knowledge of the clinical trial data management

The Clinical Development Associate will be responsible for partnering with the cross-functional study team to develop the clinical strategy/plan that leads the study team in the execution of clinical trials within the clinical plan. This role will also be responsible for supporting non-trial, trial and project level assignments within the team. The ability to ensure quality on-time fulfillment of deliverables is essential for this position. DUTIES AND RESPONSIBILITIES " Plans and executes trial-level

Job Responsibilities: The Associate Clinical Project Manager will support the Clinical Project Manager in all operational aspects of nutritional clinical trials. Responsibilities will include, but will not be limited to: Participate in the design of the case report forms and source documents for a study and the writing of informed consents. Participate in the review of essential study documents from study sites such as clinical study protocols, Case Report Forms (CRFs), informed consent forms, and source documents

MAKRO delivers custom client-centric solutions by offering contract outsourcing and premium staffing to the most well known life science organizations throughout United States. Our broad geographic reach, scalability and immense talent pool enable us to reliably meet the needs of enterprise-level clients. We at MAKRO thoroughly understand and believe that long lasting in-depth relationships with clients is an integral part in the business environment. Our vision is to become a most reliable 'connector' between

Indianapolis Indiana As an Industry Leader in Healthcare known...

Qualifications - B.A / B.S degree in a related field. - Experience with Oracle Clinical and ClinTrials. - Phase Forward InForm experience. - Experience with Medidata RAVE. - Significant clinical data programming experience or related experience. - Proficiency in database set-up and programming relating to area of expertise. - Able to program data listings and manipulate data in SAS (SAS Programming area of expertise). - Self-motivated, willing to learn and demonstrates success at current job

Qualifications - B.A / B.S degree in a related field. - Experience with Oracle Clinical and ClinTrials. - Phase Forward InForm experience. - Experience with Medidata RAVE. - Significant clinical data programming experience or related experience. - Proficiency in database set-up and programming relating to area of expertise. - Able to program data listings and manipulate data in SAS (SAS Programming area of expertise). - Self-motivated, willing to learn and demonstrates success at current job

Qualifications - B.A / B.S degree in a related field. - Experience with Oracle Clinical and ClinTrials. - Phase Forward InForm experience. - Experience with Medidata RAVE. - Significant clinical data programming experience or related experience. - Self-motivated, willing to learn and demonstrates success at current job. - Excellent people and communication skills (written and oral). - Extensive experience and understanding of lab and other third-party data regarding to his/her area of expertise

Qualifications - B.A / B.S degree in a related field. - Experience with Oracle Clinical and ClinTrials. - Phase Forward InForm experience. - Experience with Medidata RAVE. - Significant clinical data programming experience or related experience. - Self-motivated, willing to learn and demonstrates success at current job. - Excellent people and communication skills (written and oral). - Extensive experience and understanding of lab and other third-party data regarding to his/her area of expertise

Qualifications - Prefer BS/BA. - 1 year monitoring experience or combination of on-site monitoring and clinical research coordinator experience. - Customer service orientation. - Sound knowledge of medical terminology and clinical monitoring process. - In depth therapeutic and protocol knowledge as provided in company training. - Ability to perform regionalized travel an average of 65%, depending on project needs. - Excellent verbal and written communications skills.

Clinical Research Associate (CRA) - part time Description: Everyday, Volt Life Sciences (VLS) partners with the most respected and innovative companies in the scientific and clinical research community to assist them in their goal of sustaining and improving life. Our customers' quest for new medical breakthroughs, our candidates' aptitude for achievement and our ability to bring the two together have made us the choice partner for WorkforceDesign in the bio-technology, pharmaceutical, and medical device

Clinical Project Manager / Sr Project Manager Description: Volt Life Sciences (VLS) partners with the most respected and innovative companies in the scientific and clinical research community to assist them in their goal of sustaining and improving life. Our customers' quest for new medical breakthroughs, our candidates' aptitude for achievement and our ability to bring the two together have made us the choice partner for Workforce Designs in the bio-technology, pharmaceutical, and medical device industries