better Biotech Pharma Job in Illinois

State of Illinois license as a Registered Pharmacist required...

experienced Clinical Data Manager in North Chicago Illinois...

Senior Clinical Research Associate in North Chicago Illinois...

with a good attitude in North Chicago Illinois...

their team in Northern Suburb of Chicago Illinois...

This position is NonExempt. Hours over 40 will be paid at Time and a Half. Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year. The primary goals are to provide accurate data acquisition and to furnish accurate and well-documented study databases to the statistical and clinical teams. Also includes Case Report Forms; initiating the purchase of CRFs, diaries, and related documents from clinical protocols, preparing the study database

A Pharmaceutical company has an immediate opening for a Senior Clinical Research Associate in North Chicago Illinois...

SUMMARY: Responsible for coordinating and managing contracted homecare services in the support of sponsored projects and Phase 1 IV clinical studies in a variety of therapeutic areas ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: Other duties may be assigned. Assist in developing study / project support information, i.e. proposals, training manuals, data collection forms, Physician Order forms Identify resources (e.g. homecare agencies) for contracted study services

A Pharmaceutical company has an immediate opening for an experienced Clinical Data Manager in North Chicago Illinois...

A global healthcare and pharmaceutical company has an immediate need for a In-House Clinical Research Associate (CRA). Clinical Research Associates will be responsible for assisting Clinical Project Manager's with day-to-day activities that support global clinical research trials. CRA's are office-based with low travel (around 20%). Major job duties include: File and track clinical documents and trial master files. Participate in clinical trial meetings. Track and update clinical trial activities. Receive

Travel 25 Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

Travel 5 Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

Travel 20 Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

is desired Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

Travel 20 Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

10 25 Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

RN in Illinois or ability to become registered in Illinois...to 10 Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

0 10 Country USA State Province Region Illinois Site Location For corporate headquarters positions please...

with a good attitude in North Chicago Illinois...

Job Classification: Contract Description: A global healthcare and pharmaceutical company has an immediate need for a In-House Clinical Research Associate (CRA). Clinical Research Associates will be responsible for assisting Clinical Project Manager's with day-to-day activities that support global clinical research trials. CRA's are office-based with low travel (around 20%). Major job duties include: File and track clinical documents and trial master files. Participate in clinical trial meetings. *

This position is NonExempt. Hours over 40 will be paid at Time and a Half. Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year. The primary goals are to provide accurate data acquisition and to furnish accurate and well-documented study databases to the statistical and clinical teams. Also includes Case Report Forms; initiating the purchase of CRFs, diaries, and related documents from clinical protocols, preparing the study database

FT Clinical Pharmacist Jobs in Central Illinois Job Location Decatur Illinois Category Pharmacy Staff Pharmacist Apply Now...

Knowledge Registered Pharmacists in the state of Illinois or eligible for same...

Knowledge Registered Pharmacists in the state of Illinois or eligible for same...

Clinical Research Associate C to their team in Northern Suburbs of Chicago Illinois...

This position is NonExempt. Hours over 40 will be paid at Time and a Half. Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year. The primary goals are to provide accurate data acquisition and to furnish accurate and well-documented study databases to the statistical and clinical teams. Also includes Case Report Forms; initiating the purchase of CRFs, diaries, and related documents from clinical protocols, preparing the study database

Clinical Research Associate CRA Sr CRA Illinois 0805976 Apply Online Description The Clinical Development...Profile Locations USA Illinois Chicago Organization USA02 US Clinical Development Svcs...

JOB PURPOSE/SUMMARY: Serves as the primary Kendle CDM contact with Sponsors and represents CDM on project teams. Responsible for project timelines, deliverables, financial results, reporting and overall quality. Primary responsibility for Level 4 Balanced Score Card (Biometrics stand-alone). Responsible for the creation and maintenance of CDM project budgets and essential CDM documents for assigned projects. Approves the building, testing and validation of clinical databases. Coordinates the receipt and processing

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Develop Case Report Forms for clinical trials Present (e.g. study specific guidelines and procedures, case report forms

Clinical Research Coordinator KSR-Clinical Research is seeking a clinical research coordinator in the greater Chicagoland area. The CRC will: - Coordinate effective communication between data management and CRO to ensure timely design and delivery of CRFs, database(s), and the data management plan; - Understand and implement clinical protocols, CRFs, and other documents pertinent to study conduct day-to-day supervision of defined aspects of the study, such as recruitment activities or randomization status

Join one of the fastest-growing, successful Pharmaceutical organizations in the world. Currently, this organization is seeking multiple Regional Clinical Research Associates to perform field monitoring visits in a 3-5 state region. Enjoy a competitive benefits package, a work/life balance and the opportunity for extensive professional development. - 8-10 site visits per month - any therapeutic background will be considered - second-to-none industry training. Job Requirements: Viable candidates

About Us: Clinical Resource Network, LLC specializes in the provision of in-home nursing, pharmacy and phlebotomy services to facilitate clinical trials. We centrally manage these services to support Phase I-IV clinical trials conducted in the US, Canada, and Europe. We support trials in all therapeutic categories and in all age groups by providing protocol-related tests, assessments or drug administration in the patient s home or workplace. Currently, we are searching for a Clinical Research Associate (CRA

Clinical Research Coordinator KSR-Clinical Research is seeking a clinical research coordinator in the greater Chicagoland area. The CRC will: - Coordinate effective communication between data management and CRO to ensure timely design and delivery of CRFs, database(s), and the data management plan; - Understand and implement clinical protocols, CRFs, and other documents pertinent to study conduct day-to-day supervision of defined aspects of the study, such as recruitment activities or randomization status

Florida Dallas Austin and San Antonio Texas Illinois Michigan and Ohio Contract Regional Clinical Research...

This is a long term contract position based in Northern Illinois...

CLINICAL PHARMACIST Coram Specialty Infusion Services, an Apria Healthcare company is currently seeking a Registered Pharmacist to join our expert team in Mount Prospect, IL. This is an excellent opportunity for an individual looking for a clinical pharmacy environment free of the hassles associated with retail pharmacy, or the schedule of a hospital environment. Coram offers competitive wages, and a comprehensive benefit package that rivals any infusion competitor. You will perform all daily pharmacy operational

their team in Northern Suburb of Chicago Illinois...

(1789) Clinical Data Manager - C (3 Openings ACG) Overview: -Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year. -The primary goals are to provide accurate data acquisition and to furnish accurate and well-documented study databases to the statistical and clinical teams. -Also includes Case Report Forms; initiating the purchase of CRF?s, diaries, and related documents from clinical protocols, preparing the study database dictionary

Clinical Research Coordinator Description: Clinical site in Chicago, IL needs CRC to assist in running Phase IIb/III clinical trials. Must have be an experienced coordinator who is organized, experienced with EDC, strong knowledge of GCP and phlebotomy experience. Study: Urology Study; 36 week study; the first 13 weeks are the most intense Prefer: CCRC , RN/LPN When you work for Smith Hanley Consulting Group, you are partnering with a leader in clinical trials and scientific staffing. For over

Long term contract for an experienced Clinical Data Coordinator--paying to: $43.00 per hour! Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year. The primary goals are to provide accurate data acquisition and to furnish accurate and well-documented study databases to the statistical and clinical teams. Also includes Case Report Forms; initiating the purchase of CRF s, diaries, and related documents from clinical protocols

Clinical Research Associate: Perform all clinical research activities including data collection, monitoring of study participants, data entry and data quality control. When appropriate, work with the study nurse to order and assure scheduling of all tests required for study entry and will assure that the results meet specific protocol criteria prior to patient enrollment. Prepare for and participate in all audits and reviews of their program.

Follow your aspirations to Abbott for diverse opportunities, competitive salaries, great benefits, a 401(k) retirement savings plan, a company paid pension plan and profit sharing, all with a company providing the growth and strength to build your future. This is an excellent opportunity for an seasoned clinical research professional to apply established skills with developmental products through managing new and existing clinical studies. The incumbent will initiate and coordinate study start-up activities

This position is responsible for the accurate delivery of pharmacy services which include dispensing of medications, quality assurance, clinical monitoring, and control of inventory. Ensures that the pharmacy operates in accordance with Federal/State regulations, JCAHO standards, as well as company policies.. Job Requirements: Duties: Pharmacy knowledge; Microsoft Office literacy; Excellent oral and written communication skills; 1-3 years experience in retail, hospital, or managed care setting. Exposure to

Kendle, a leading clinical research organization, is seeking experienced Clinical Research Associates (CRAs) with one to four years of regional site monitoring experience. Kendle offers a travel expectation of 60 - 80% averaging up to three overnight stays per week, career advancement that can be home-based up to and including Project Leader (Project Manager) as well as a company core value to have a balance between work and life. Key Responsibilities CRAs at Kendle complete project activities associated

Description Asen computer associates has been in business for over 30 years. We are a preferred vendor for our clients and we pride ourselves in our ethical values. We strive to present the best candidates for our clients. This position is for our fortune 500 Pharmaceutical client in the North suburbs of Chicago. We provide candidates for both clinical and IT. I am the SR recruiter for Asen and have been servicing this client on both IT and clinical for over 5 years. If interested in this position please

This is a Home Based CRA role that can be located anywhere within the Central United States. The Senior Clinical Research Associate performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products and/or medical devices. Conducts site visits to determine protocol and regulatory compliance, and prepares required documentation. Represents PPD in the global medical research community and develops collaborative

Candidate must have a minimum of 3 years experience in Data Management including preparation of CDM plans, review draft protocols, CRF Design and review, etc. The candidate will also be responsible for generating paper and electronic queries to appropriate internal and external personnel, sites, vendors, CRA's and the candidate must also be able to act as a lead Data Manager for multiple projects.. Job Requirements: Must have 2-3 years of Clinical Data Coordinator experience. Cleaning data, generating queries

Astellas is the bright spot in the pharmaceutical industry - not just because of what we do, but in the way we do it. If you are looking for a company where you can change a life, make a dream come true, and light the way for a better tomorrow, Astellas is the place where you can shine. We offer a different kind of work culture. A high standard of ethics is mandatory. Quality is our pledge. Diversity is valued. Individual initiative is rewarded. Astellas offers an environment where our employees can make a real

Senior Clinical Research Associate - Bannockburn Location The Senior Clinical Research Associate will report to the Executive Director, Clinical Affairs and will work in matrix team with Program Managers. The Sr. Clinical Research Associate is responsible for managing, implementing and monitoring clinical studies in a team setting. Member of the clinical team responsible for conducting Phase I - IV studies according to Federal Regulations and ICH guidelines and study protocol, including planning study conduct

Do you want a job that s not just a job, but a career? Are you looking for a chance to grow professionally? If so, we want to hear from you! About Us: Clinical Resource Network, LLC specializes in the provision of in-home nursing, pharmacy and phlebotomy services to facilitate clinical trials. We centrally manage these services to support Phase I-IV clinical trials conducted in the US, Canada, and Europe. We support trials in all therapeutic categories and in all age groups by providing protocol-related