better Biotech Pharma Job in Minnesota

Director Biostatistics and Data Management Req. Code : 721 Division/Department : CARDI Location : Plymouth MN US 55442 Travel Required : None Job Type : Full Time Career Level : Manager (Manager/Supervisor of Staff) Education : Master's Degree Category : Biotechnology and medical device Job Description : At ev3 we’re committed to developing innovative endovascular technologies for coronary, peripheral and neurological applications. Creative, competent people with a passion for enhancing healthcare around

A leading Fortune 100 pharmaceutical client of ours has an opening for a Regional CRA based in Minneapolis, MN. Job DescriptionDelivery of high quality data according to agreed time lines and budget, ensuring adherence to international and local regulations and the client's SOP standards. Demonstrate exceptional customer focus as evidenced by positive feedback from the client's colleagues and external customers (Investigators). Participate in the site nomination process; perform evaluation of site capability

Clinical Research Mgr.-Women's Pelvic HealthMinnetonka, MN 11/11/2008 Clinical Studies & Field Clinical Research 125-08 POSITION DESCRIPTION: This position oversees a portfolio of clinical studies, data activities, and strategies for an entire therapeutic area of AMS technologies by providing leadership and management of a team of clinical professionals who are responsible for the design, planning, implementation and reporting of all human clinical studies and data activities for that therapeutic area(s). The

Clinical Operations Manager - (26656) Requisition Number: 26656 Location: MN, Minneapolis Job Description: Great Opportunity for a leadership position at our Headquarters (Minneapolis, MN) LifeWorks Organization! Read on to find out more!! Clinical background and management experience in operations. 1. Leadership Responsibilities within Service Delivery Comprehensive understanding of LifeWorks mission and vision and the ability to effectively communicate this throughout service delivery. Strong management

Sr. Clinical Research Associate Requisition ID 27096 Full/Part Time Location Maple Grove, MN Description Senior Clinical Research Associate - Field-based - Ohio Region Delivering on the promise of medical innovation begins at Boston Scientific! By delivering innovative products that help clinicians improve the lives of patients every single day, Boston Scientific makes a profound impact on the quality of medical care around the world. Join a global organization that is fueled by the diversity and talent of

Clinical Project Manager - Arden Hills Requisition ID 25361 Full/Part Time Location Maple Grove, MN Description Clinical Project Manager Delivering on the promise of medical innovation begins at Boston Scientific! By delivering innovative products that help clinicians improve the lives of patients every single day, Boston Scientific makes a profound impact on the quality of medical care around the world. As we continue to transform the field of medical technology, we seek dedicated individuals who possess the

-Biostatistician is responsible for writing stat plans for clinical protocols -SAS programming -Data collections using Clindex -Standard bio-statistical analysis -Working on 4 - 8 projects at a time Qualifications: -2+ years experience in a medical device company -Proficiency with SAS programming -Experience writing stat plans for study protocols -Experience with Clindex -Understanding of Regulatory strategy -Ability to work 40 hours a week -Ability to handle multiple projects at the same time Join Aerotek

AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease. Clinical Research Associate III City:Plymouth Relocation Available:No State/Province:MN Country:United States Type (Duration):Regular, Full Time Job Number:1294 Functional Area:Clinical Division:Clinical Work Hours:Standard As aClinical Research

Clinical Research Associate CRA Sr CRA Minnesota 0805980 Apply Online Description The Clinical Development...Profile Locations USA Minnesota Minneapolis Organization USA02 US Clinical Development Svcs...

Sr Clinical Research Manager Requisition 65043 Category Clinical Studies Business Neuromodulation Division Neurological Clinical Location USA-MN-Mpls-Fridley Relocation Relocation eligibility to be determined Job Type Full Time - Regular Exempt/Non-Exempt Exempt Shift First Travel Percentage 20 - 30% Experience Required 6 years Education Required Bachelors Degree Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description The Senior Clinical Research Manager will support clinical studies

Clinical Research Director Requisition 62585 Category Clinical Studies Business Neuromodulation Division Neurological Clinical Location USA-MN-Mpls-Fridley Relocation Relocation eligibility to be determined Job Type Full Time - Regular Exempt/Non-Exempt Exempt Shift First Travel Percentage less than 10% Experience Required 10+ years Education Required Bachelor of Science Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description The Clinical Research Director will create a competitive

Responsibilities: Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! You will be supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and our client's company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your

Responsibilities: Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! You will be supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and our client's company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your

Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! You will be supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and our client's company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal

Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! You will be supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and our client's company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal

Making great happen. Work with great people and be challenged to reach your potential. We depend on highly skilled and enthusiastic achievers like you to provide innovative solutions for thousands of companies and twenty five million employees worldwide. By fostering values that promote freedom and flexibility we encourage professional growth and offer rewarding career opportunities. Innovate, lead, and grow by doing what you love to do. EEO/M/F/D/V Great Opportunity for a leadership position at our Headquarters

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

Clinical Operations Manager - (26656) Requisition Number: 26656 Location: MN, Minneapolis Job Description: Great Opportunity for a leadership position at our Headquarters (Minneapolis, MN) LifeWorks Organization! Read on to find out more!! Clinical background and management experience in operations. 1. Leadership Responsibilities within Service Delivery Comprehensive understanding of LifeWorks mission and vision and the ability to effectively communicate this throughout service delivery. Strong management

Manager Clinical Research Hill-Rom Holdings, Inc. is the parent company for Hill-Rom's operations and has been a leading worldwide manufacturer and provider of medical technologies and related services for the health care industry, including patient support systems, non-invasive therapeutic products for a variety of acute and chronic medical conditions, medical equipment rentals, and information technology solutions since 1929. Hill-Rom Holdings, Inc. (NYSE:HRC) currently employs more than 6,500 people

YOUR CAREER CAN MAKE A LIFE-SAVING DIFFERENCE The National Marrow Donor Program (NMDP) is a leader in the fast-growing field of cellular transplantation. Everyday, more than 6,000 children and adults are searching for a second chance at life due to a devastating illness such as leukemia, lymphoma or other threatening disease. These patients seek the resources of the NMDP with the hope of receiving a life-saving marrow or cord blood transplant. Our staff helps deliver cutting-edge science, service and support

At ev3 we re committed to developing innovative endovascular technologies for coronary, peripheral and neurological applications. Creative, competent people with a passion for enhancing healthcare around the globe have driven our success. Join us as we grow by making a meaningful difference. We are currently seeking a Director of Biostatistics and Data Management. This position is responsible for the coordination and development of all statistics and data management activities related to clinical studies conducted

AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease. As a Sr. Clinical Research Associate, you will design, implement, monitor and close out clinical investigations. Support professionalism and scientific expertise of department. - Follow department Standard Operating Procedures. - Set

AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease. As a Clinical Research Associate you will implement and carry out functions of clinical research. - Schedule and conduct monitoring activities at assigned centers assessing site compliance to the clinical investigation plan, regulations and

AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease. As a Clinical Research Associate, you will implement and carry out functions of clinical research. - Schedule and conduct monitoring activities at assigned centers assessing site compliance to the clinical investigation plan, regulations

Making great happen. Work with great people and be challenged to reach your potential. We depend on highly skilled and enthusiastic achievers like you to provide innovative solutions for thousands of companies and twenty five million employees worldwide. By fostering values that promote freedom and flexibility we encourage professional growth and offer rewarding career opportunities. Innovate, lead, and grow by doing what you love to do. EEO/M/F/D/V Great Opportunity for a leadership position

YOUR CAREER CAN MAKE A LIFE-SAVING DIFFERENCE The National Marrow Donor Program (NMDP) is a leader in the fast-growing field of cellular transplantation. Everyday, more than 6,000 children and adults are searching for a second chance at life due to a devastating illness such as leukemia, lymphoma or other threatening disease. These patients seek the resources of the NMDP with the hope of receiving a life-saving marrow or cord blood transplant. Our staff helps deliver cutting-edge science, service and support

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

The health plan clinical pharmacist positively impacts formulary decisions by compiling, evaluating and presenting clinical drug information and serves as a drug information resource for internal staff, external customers, and the Pharmacy and Therapeutics Committee. Whether you are a new graduate or experienced clinical pharmacist this is an opportunity to make a positive impact to health care! In this highly visible role the successful candidate will provide cost effective pharmaceutical care to Rocky

The health plan clinical pharmacist positively impacts formulary decisions by compiling, evaluating and presenting clinical drug information and serves as a drug information resource for internal staff, external customers, and the Pharmacy and Therapeutics Committee. Whether you are a new graduate or experienced clinical pharmacist this is an opportunity to make a positive impact to health care! In this highly visible role the successful candidate will provide cost effective pharmaceutical care to Rocky

Making great happen. Work with great people and be challenged to reach your potential. We depend on highly skilled and enthusiastic achievers like you to provide innovative solutions for thousands of companies and twenty five million employees worldwide. By fostering values that promote freedom and flexibility we encourage professional growth and offer rewarding career opportunities. Innovate, lead, and grow by doing what you love to do. EEO/M/F/D/V Great Opportunity for a leadership position

Our customer is a medical device company in the Minneapolis/St. Paul area that is going through a period of tremendous growth. This company seeks a Clinical Project Manager to add to their team. In this combination role, the incumbent will be responsible for participating in site and vendor management, protocol development, and clinical site monitoring. This is an exceptional opportunity for a seasoned CRA with some management experience to join a tenured and collaborative organization that will only grow

Our customer is a medical device company in the Minneapolis/St. Paul area that is going through a period of tremendous growth. This company seeks a Clinical Project Manager to add to their team. In this combination role, the incumbent will be responsible for participating in site and vendor management, protocol development, and clinical site monitoring. This is an exceptional opportunity for a seasoned CRA with some management experience to join a tenured and collaborative organization that will only grow

Job Description: Humana Inc., headquartered in Louisville, Kentucky, is one of the nation's largest publicly traded health benefits companies. Humana offers a diversified portfolio of health insurance products and related services - through traditional and consumer-choice plans - to employer groups, government-sponsored plans, and individuals. Today, Humana is a leader in consumer engagement. Throughout its diversified customer portfolio, the company provides guidance that can both help lower costs and lead

We are headquartered in Eagan Minnesota with locations in Nebraska New Mexico Texas and Illinois...

Principal Biostatistician Cary North Carolina Eden Prairie Minnesota Indianapolis Indiana Lexington Kentucky Lenexa Kansas San...

We are headquartered in Eagan Minnesota with locations in Nebraska New Mexico Texas...

Humana Inc., headquartered in Louisville, Kentucky, is one of the nation's largest publicly traded health benefits companies. Humana offers a diversified portfolio of health insurance products and related services - through traditional and consumer-choice plans - to employer groups, government-sponsored plans, and individuals. Today, Humana is a leader in consumer engagement. Throughout its diversified customer portfolio, the company provides guidance that can both help lower costs and lead to a better health

Manager Clinical Research Hill-Rom Holdings, Inc. is the parent company for Hill-Rom's operations and has been a leading worldwide manufacturer and provider of medical technologies and related services for the health care industry, including patient support systems, non-invasive therapeutic products for a variety of acute and chronic medical conditions, medical equipment rentals, and information technology solutions since 1929. Hill-Rom Holdings, Inc. (NYSE:HRC) currently employs more than 6,500 people

(Job #20614) Perform clinical monitoring process in accordance with GCP s and SOP s to assess efficacy and safety. You ll manage clinical projects to timelines/ budgets, assist in managing the selection process of clinical investigators, ensure proper collection of study data/analysis, and prepare manuscripts for publication. Bachelor s degree in nursing, science or engineering or associate s degree with relevant experience and minimum three years experience in clinical research, preferably as a CRA or research

AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease. As a Clinical Research Associate, you will implement and carry out functions of clinical research. - Schedule and conduct monitoring activities at assigned centers assessing site compliance to the clinical investigation plan, regulations

AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease. As a Sr. Clinical Research Associate, you will design, implement, monitor and close out clinical investigations. Support professionalism and scientific expertise of department. - Follow department Standard Operating Procedures. - Set

AGA Medical Corporation, a medical technology company, is dedicated to the development, design, manufacture, and marketing of nitinol-based occlusion devices and accessories for the minimally invasive treatment of cardiovascular defects and peripheral vascular disease. As a Clinical Research Associate you will implement and carry out functions of clinical research. - Schedule and conduct monitoring activities at assigned centers assessing site compliance to the clinical investigation plan, regulations and

Clinical Research Associate We are in need of several highly qualified Clinical Research Associates The ideal candidates must have experience basic medical and business knowledge. Desired competency in clinical research or having demonstrated adequate level of proficiency within the CRA II competency profile. Understands and can apply knowledge of clinical trial designs to trial execution. Knowledge and experience in international standards (GCP/ICH), international (FDA, EMEA) and local regulations. Expertise

Organizes and supervises new clinical studies. Acts as primary author for clinical study protocols and supporting documents (informed consent, case report forms, training materials, etc). Investigator, IRB and IACUC approval contacts for both human and animal studies. Primary responsibility for recruitment, selection, and training of clinical investigators with respect to protocol and data submission requirements. Responsible for completing appropriate Study Organizer forms (i.e. Request for CRD number,

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 Statprobe provides a full range of data management and biostatistical services for the pharmaceutical and biotechnology industries. We not only pay relentless attention to the details, we also lend a broader perspective

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 - 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

At ev3 we re committed to developing innovative endovascular technologies for coronary, peripheral and neurological applications. Creative, competent people with a passion for enhancing healthcare around the globe have driven our success. Join us as we grow by making a meaningful difference. We are currently seeking a Director of Biostatistics and Data Management. This position is responsible for the coordination and development of all statistics and data management activities related to clinical studies conducted