better Biotech Pharma Job in Michigan

Company: Barbara Ann Karmanos Cancer Institute Facility: Harper Professional Building at Detroit Department: Clinical Trials Provide data management/regulatory specialist support to Clinical Trials Office, with level of supervision correlated to both performance and experience. Assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines. Maintain logs and update the Clinical Trials Office Oncore database in a timely manner. Respond

Company: Barbara Ann Karmanos Cancer Institute Facility: Karmanos In-Patient Units at Detroit Department: 10 WN Bone Marrow Transplant Unit Provide data management/regulatory specialist support to Clinical Trials Office, with level of supervision correlated to both performance and experience. Assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines. Maintain logs and update the Clinical Trials Office Oncore database in a timely

Job Title: Clinical Research Coordinator Job Title Description: Clinical Research Coordinator Location: Ann Arbor, MI Division: THI Ann Arbor, MI Job Type: Regular Description: Terumo Heart, Inc. is a growing subsidiary of a multi-billion dollar, global medical products company. We manufacture, distribute and market high-quality capital equipment and consumable medical devices. Working in an industry where we have a tangible difference in people's lives is one of the most rewarding things about working at our

Clinical Research Associate CRA Sr CRA Michigan 0805979 Apply Online Description The Clinical Development...Profile Locations USA Michigan Ann Arbor Organization USA02 US Clinical Development Svcs...

Profile Locations USA Michigan Ann Arbor Organization USA02 US Clinical Development Svcs...

Collaborative for Health based in Ann Arbor Michigan...SUPERVISION RECEIVED Supervision is received from the Japan DOPPS Project Manager based in Ann Arbor Michigan...

Clinical Research Associate CRA Sr CRA Michigan The Clinical Development Services division of Quintiles...Job Requirements Clinical Research Associate CRA Sr CRA Michigan Prefer BS BA...

Requires State of Michigan Pharmacist and Controlled Substance licensure...

Clinical Research Coordinator (CRC) Kelly Scientific Resources (KSR) currently has an exciting Direct Hire Clinical Research Coordinator (CRC) opportunity available in the Ann Arbor, MI area! Our client is a subsidiary of a multi-billion dollar global medical products company. Competitive salaries, generous benefits (401(k), tuition reimbursements and health/vision/dental plans) are provided! Please see below for more details and click 'Apply Now!' for immediate consideration. Description: This position

Clinical Research Coordinator (CRC) Kelly Scientific Resources (KSR) currently has an exciting Direct Hire Clinical Research Coordinator (CRC) opportunity available in the Ann Arbor, MI area! Our client is a subsidiary of a multi-billion dollar global medical products company. Competitive salaries, generous benefits (401(k), tuition reimbursements and health/vision/dental plans) are provided! Please see below for more details and click 'Apply Now!' for immediate consideration. Description: This position

Qualified candidates will have a B S in Pharmacy or a PharmD with a current Michigan State Pharmacist license...

Home based Opportunities Available! Statewide! 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

Home based Opportunities Available! Statewide! 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

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

Founded in 1963, BIOTRONIK, Inc. is a pioneer in developing innovative technologies and medical devices that save and enhance the quality of life for millions of individuals living with cardiovascular conditions. With a growing base of over 4,100 employees worldwide, we're continually looking for talented professionals with the passion and drive for excellence to join our mission. BIOTRONIK, Inc. now has multiple exciting opportunities available for Regional Clinical Research Associates. POSITION

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

Director of Clinical Development This exciting opportunity will give you the chance to build and mold the clinical division within a smaller biopharmaceutical company under your direction and vision. This individual must have clinical trial experience, and Infectious Disease background, and a vision to build and create a clinical program. Responsibilities To design, supervise, and conduct clinical strategy including protocol development, safety monitoring, statistical strategy and consistent management

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

Qualifications Qualifcations: - B.A./B.S. Degree in related field, or an equivalent combination of education and work experience - Five + years relevant clinical data management experience - Previous management experience or demonstrated leadership ability - Ability to work in and lead multi-disciplinary/cultural teams - Proven ability to effectively recruit and develop staff - Proficient in the use of the clinical data management systems used at i3 Statprobe - Ability to prioritize

Qualifications Qualifications: - MS degree required with a minimum of five years experience in statistics or PhD with two years of experience in statistics - Ability to work in a fast-paced, team-oriented environment - Computer proficiency is required - Ability to perform statistical analyses of clinical data - Ability to define problems, collect data, establish facts, and draw valid conclusions - Ability to interpret an extensive variety of technical instructions in mathematical or

Qualifications Qualifications - Demonstrated ability to manage multiple tasks. - Demonstrated strong teamwork skills and ability to influence others. - Demonstrated strong attention to detail and accuracy of work. - Demonstrated learning agility. - Excellent written and verbal communication skills. - Working knowledge of clinical trial processes with emphasis on data collection and reporting of clinical trial data. - Demonstrated ability to quickly learn technical databases

Qualifications - BA or BS with a science, statistics or health-related background is required. Equivalent experience in data management and a medical-related field may be substituted - 5 years experience managing research data in a scientific/health research related field is required - Oracle Clinical development proficiency is required - SAS experience a plus - Knowledgeable and expert in all areas of database setup and programming for clinical studies - Familiarity with data management processes

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.