better Research Development Job in Minnesota

Piper Jaffray is a client-focused, leading middle market investment bank and institutional securities firm founded in 1895. The middle market is driven by the energy of entrepreneurship. At Piper Jaffray, our clients include the middle market's most dynamic companies. Guiding innovative organizations leaves no room for mediocrity, and with 1,200 employees worldwide, each one of us makes an impact every day. Our entrepreneurial culture means that individuals have a meaningful impact collaborating across business

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. Sr. Clinical Research Associate City:Plymouth Relocation Available:No State/Province:MN Country:United States Type (Duration):Regular, Full Time Job Number:1307 Functional Area:Clinical Division:Clinical Work Hours:Standard As aSr. Clinical

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

1256 Functional Area Research Development Division Research Development Work Hours Standard As aPrincipal R...Time Job Number 1256 Functional Area Research Development Division...

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 II City:Plymouth Relocation Available:No State/Province:MN Country:United States Type (Duration):Regular, Full Time Job Number:1222 Functional Area:Clinical Division:Clinical Work Hours:Standard As aClinical Research

Sr R&D Engineer Requisition ID 27365 Full/Part Time Location Maple Grove, MN Description Job Purpose: This position focuses on catheter product development including; project planning, innovative concept design, prototype fabrication, testing, analysis and reporting. Compiles and analyzes operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials. Provides direction to other team members consistent with goals and objectives of project

Senior Research Associate - Preclinical Requisition ID 27410 Full/Part Time Location Maple Grove, MN Description 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 its entire workforce General Summary: The Senior Research Associate is an expert responsible for independent management of complex projects

Senior Research Associate - Preclinical Requisition ID 27163 Full/Part Time Location Maple Grove, MN Description 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 its entire workforce. General Summary: The SRA is an expert responsible for independent management of complex projects. The position

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

We are located in NE Minneapolis just minutes from the University of Minnesota and downtown area...

-Clinical Research Associate will schedule and conduct monitoring activities at assigned centers assessing site compliance to the clinical investigation plan, regulations and GCPs, as needed. -Responsible for obtaining all relevant source data for adverse events and deaths, as needed. -Assist in the writing of AE/Death Summaries. Follow-up with any adverse event issues identified by the medical advisor. -Independently develop and implement corrective and preventive actions at sites and provide continuous

A Pharmaceutical company specializing in Women's Health has an immediate need for a Regional home based CRA. *60% travel *Contract of 1 year (possibly extended to 3 years) *Home based and ALL sites located in North Central region Monitoring Responsibilities: - Implementation and monitoring of the clinical trial at selected sites - Conduct site visits pre-study, study initiations, and to study close out - Ensure Case Report Forms (CRF) are reviewed and completed - Planning and implementing all activities required

There is an immediate need for a Research Assistant I at a company that provides microbiology and virology efficacy testing services to clients who develop antimicrobial and products. Minimum Requirements: Bachelors Degree in Biology or related field. 1+ year of Microbiology in the industry; specifically with Aseptic Technique Must be detail oriented and high attention to detail Responsibilities: Performs chemical and germicidal efficacy testing utilizing classical microbiological techniques Performs

Development Specialist Requisition Number 08 3171 State Minnesota City Minneapolis Shift Shift 1 Job Description...

Researcher/Pharmacist for i3 Innovus 218048 Job Description Submit Description Researcher/Pharmacist i3 Innovus Eden Prairie, MNor home based with experience i3 Innovus, a division of Ingenix, provides a scientific view of the marketplace, giving an expert perspective to help pharmaceutical companies make smart decisions about their products. With recognized experience in health economics and outcomes, data analysis, and strategic consulting, i3 Innovus delivers the scientific evidence that helps products

Analyst Job Reference 44804BR Location United States Minnesota City Minneapolis Function Category Portfolio and Fund...Working within the Growth Investors business of UBS Global Asset Management this role is based in Minneapolis Minnesota...

General Summary: The SRA is an expert responsible for independent management of complex projects. The position requires a mastered skill set allowing for independent reporting and regulatory submissions. The SRA provides analytical interpretation and provides recommendation of study outcomes to the Core teams and PC management. Mentors others within immediate preclinical group Minimum Education & Experience: Education: Bachelors Degree Biology or Veterinary Technology, Masters Preferred. Professional Exp

Job Category:Health Economics & Outcomes Reference Code:218048 Position Type:Full-time Researcher/Pharmacist for i3 Innovus - 218048 Job Description Description Researcher/Pharmacisti3 InnovusEden Prairie, MN or home based with experience i3 Innovus, a division of Ingenix, provides a scientific view of the marketplace, giving an expert perspective to help pharmaceutical companies make smart decisions about their products. With recognized experience in health

Position Description The Product Development Principal Clinical Research Specialist is responsible for developing strategies and driving processes to meet the Product Commercialization Process clinical requirements. Working with Medtronic Neuromodulation Product Development staff and some of the leading physicians in their fields of expertise, the Product Development Principal CRS will work on some of the newest technologies and applications being developed in the areas of direct drug delivery, spinal cord

Position Responsibilities Assures successful implementation of assigned studies consistent with Research Development program plans...

Assoc Clinical Research Spec Requisition 65099 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 10 - 20% Experience Required 1 year Education Required Bachelors Degree Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description The Associate Clinical Research Specialist works closely with

Clinical Research Specialist Requisition 64336 Category Clinical Studies Business Neuromodulation Division Neurological Clinical Location USA-MN-St. Paul-Shoreview Relocation No relocation assistance Job Type Full Time - Regular Exempt/Non-Exempt Exempt Shift First Travel Percentage less than 25% Experience Required 3 years Education Required Bachelors Degree Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description The Clinical Research Specialist (CRS) is either an assistant to

Prin Clinical Research Spec Requisition 63965 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 0% Experience Required 8 years Education Required Bachelor of Science Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description The Product Development Principal Clinical Research Specialist is

Prin Clinical Research Spec Requisition 63601 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 25 - 50% Experience Required 6 years Education Required Bachelors Degree Medtronic is an Equal Opportunity/Affirmative Action Employer Position Description The Principle Clinical Research Specialist is responsible for

Position Responsibilities Assures successful implementation of assigned studies consistent with Research Development program plans...

Postdoctoral Research Fellow Job ID 10495 Department RHSC S&B for Alzheimer Gro City St. Paul, MN Location RH - Regions Hospital & Clinics Position Type Temporary Full-Time Anticipated Work Schedule 9-5 M-F Shift Day Hrs/Pay Period 80 Job Description Responsibilities: Fellows will participate in the design, implementation and evaluation of research projects. Qualifications: Applicants need an M.D. or Ph.D. degree. Research experience in neuroscience, neuroanatomy, pharmacology, biochemistry or related field

Research Associate Md-Phd Job ID 10929 Department Alzheimer's Dept City St. Paul, MN Location RH - Regions Hospital & Clinics Position Type Full-Time Anticipated Work Schedule M-F Day Shift Shift Day Hrs/Pay Period 80 Job Description Responsibilities:Responsible for independently designing studies, implementing and conducting experiments, analyzing and interpreting data, and publishing results. This position will be expected to submit grant proposals to funding agencies. In addition, the Research Associate

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

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...

Executes the components of a study with direction from a principal investigator or supervisor, complying with regulatory laws and institutional guidelines. Prepares and edits study communications. Identifies, enrolls, and teaches study protocol participants. Responsible for accuracy and timeliness in completing study compliance activities, data collection, storage, and retrieval. Must be able to recognize defined adverse events and report to appropriate parties. (006294) Department: Cancer Center/Hematology

The RN Research Coordinator is responsible for complying with Institutional Review Board policies and procedures. Applies skills and experience towards pattern recognition of healthcare events and laboratory results supporting identification of on-going needs of the study in collaboration with other healthcare professionals. Accountable for and assures compliance throughout the research study by maintaining regulatory documentation. Assesses research protocols to determine subject eligibility. Reviews medical

This is a two year, limited tenure position that requires fluency in Spanish and English to be able to code videotapes of parent-child play sessions for a study funded by the National Institutes of Nursing Research. Executes the components of a study with direction from a principal investigator or supervisor, complying with regulatory laws and institutional guidelines. Prepares and edits study communications. Identifies, enrolls, and teaches study protocol participants. Responsible for accuracy and timeliness

Executes the components of a study with direction from a principal investigator or supervisor, complying with regulatory laws and institutional guidelines. Prepares and edits study communications. Identifies, enrolls, and teaches study protocol participants. Responsible for accuracy and timeliness in completing study compliance activities, data collection, storage, and retrieval. Must be able to recognize defined adverse events and report to appropriate parties. (006294) Department: Health Science Research-

Serves as expert resource and mentors other internal and external study/protocol personnel. Trouble shoots and resolves problems and contributes significantly to discussions on research study design, overall project management, and study results. Participates in designing, organizing, and monitoring protocols including budget elements. Independently write sections of grant applications, abstracts/posters, and manuscripts. Plans for and participates in the education of staff in areas required to carry out the

This is a limited tenure position that has been approved for 1 year that may have the possibility of turning into a regular position. Executes the components of a study with direction from a principal investigator or supervisor, complying with regulatory laws and institutional guidelines. Prepares and edits study communications. Identifies, enrolls, and teaches study protocol participants. Responsible for accuracy and timeliness in completing study compliance activities, data collection, storage, and retrieval

The Research Protocol Specialist II assists in the development and maintenance of the protocol document and process from initial receipt of participation through study completion, termination and/or publication. Responsibilities may include, but are not limited to: preparing drafts of Mayo Informed Consent Forms (ICFs), determining appropriate forms and documentation for Institutional Review Board (IRB) submission, such as participating modalities, investigational drug brochures, investigational new drug (IND

Independently executes experimental studies, after initial discussions with principal investigator, in support of lab goals, grant commitments, including independent sub-projects. Designs and troubleshoots experiments and independently determines experimental progression. Analyzes and aids in interpretation of data; authors and co-authors papers and presentations. Trains and oversees work of residents/fellows/other lab personnel. Reviews literature and customizes techniques for lab applications. (002454) Department

Provide overall management of the protocol development process from initial concept through study completion, termination and/or publication. Responsibilities include, but are not limited to: ongoing management of the protocol document and process through editing, amendments, proofing, coordination of study logistics, (i.e. blood collection kits, data collection booklets, use of CRU, etc) and verification of content to meet institutional and federal standards; communication with study sites and/or federal agencies

The Research Protocol Specialist III provides overall management of the protocol development process from initial concept through study completion and/or publication. Responsibilities include but are not limited to: ongoing management of the protocol document through editing, amendments, proofing, coordination of study logistics, (i.e. blood collection kits, data collection booklets, use of CRU, etc) and verification of content to meet institutional and federal standards; communication with study sites and/or

Travel: 20% Overview: The Packaging R&D Manager plays a key role in driving business success by providing packaging expertise and leadership on new product innovation, HMM, core renovation, and sustainabiltity initiatives for the division. In addition to managing 3 direct reports, this role also includes the development and advancement of our global Pkg R&D organization (20 developers in the field). This position will travel between the RTC and JFB facilities. Accountabilities: - Provide strategic leadership

State Canada Province MINNESOTA Country United States USA Position Type Full...

State Canada Province MINNESOTA Country United States USA Position Type Full...

Class Scientist Job Category Experienced Professional State Minnesota Relocation Available Negotiable Req Type Blue Sky...

Research Assistant I Req Number: mons-00009502 Location(s): Stanton MN Responsibilities: Monsanto is seeking a highly motivated individual with the ability to work as a part of a multidisciplinary corn breeding and testing team. The candidate will be responsible for assisting in the management of a large, multi breeder, corn research program consisting of test plot and nursery operations. Site Safety: Adhere and enforce Monsanto safety policies. Keep safety as

Research Associate, North RM/DH Req Number: mons-00009274 Location(s): Stanton MN Responsibilities: Monsanto is seeking a highly motivated individual with the ability to work as a member of a multidisciplinary corn breeding team. The primary responsibilities will be supporting the activities of breeders within the respective region and the DH breeding team. These activities will include developing advancement summaries on key breeding lines and testers; preparation

Research Associate I Req Number: mons-00009197 Location(s): Olivia MN Responsibilities: Monsanto is seeking a highly motivated individual with the ability to work as part of a multidisciplinary corn breeding and testing team. Incumbent will be responsible for assisting in the management of a comprehensive corn testing and breeding program consisting of test plot and nursery operations aimed at producing and identifying high yielding hybrids. Major responsibilities

Job Description: General Summary: The SRA is an expert responsible for independent management of complex projects. The position requires a mastered skill set allowing for independent reporting and regulatory submissions. The SRA provides analytical interpretation and provides recommendation of study outcomes to the Core teams and PC management. Mentors others within immediate preclinical group Minimum Education & Experience: Education: Bachelors Degree Biology or Veterinary Technology, Masters Preferred. Professional

Position Description The Product Development Principal Clinical Research Specialist is responsible for developing strategies and driving processes to meet the Product Commercialization Process clinical requirements. Working with Medtronic Neuromodulation Product Development staff and some of the leading physicians in their fields of expertise, the Product Development Principal CRS will work on some of the newest technologies and applications being developed in the areas of direct drug delivery, spinal cord

Research and Development Director for its Winona Minnesota based operation...

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,