Regional Cra Jobs in Butler County, Kentucky

The Fountain Group is a Professional Staffing Service We are currently seeking a Regional Clinical Research Associate for ......  More »    Fewer «   our client, Novartis - for what is anticipated to be a long term open ended contract assignment. Details for the position below Kindly respond with your updated resume should you qualify and would like to pursue. LocationNashville based CRA Travel at least 50 Seasoned Regional CRA experience required. Delivery of high quality data according to agreed timelines and budget, ensuring adherence to international and local regulations and Novartis SOP standards. Demonstrate exceptional customer focus as evidenced by positive feedback from Novartis colleagues and external customers Investigators. Participate in the site nomination process perform evaluation of site capability to deliver the contractually agreed to number of patients and high quality data then make recommendation for inclusion in the clinical trial.           Fewer «

Chicago Based Regional CRA - 4310139 Company: ConsignMed Job#: 1048 Positions: 1 Job Type: Full Time - Contract Location: ......  More »    Fewer «   Chicago - IL Department: Clinical Research Apply To This Job Email This Job Return To List Job Description Participate in the site nomination process; perform evaluation of site capability to deliver the contractually agreed to number of patients and high quality data then make recommendation for inclusion in the clinical trial. > Assume ambassadorial role to facilitate communication between sites and Novartis line functions to increase value proposition to investigators. > Facilitate preparation and collection of site level documents. > Execute site initiation and training activities. > Perform monitoring visits according to monitoring plan and author study monitoring reports. > Manage site drug supply management. > Resolve site level update of technical systems (ClinAdmin, EDC). > Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc).           Fewer «

Chicago Based Regional CRA - 4310139 Company: ConsignMed Job#: 1048 Positions: 1 Job Type: Full Time - Contract Location: ......  More »    Fewer «   Chicago - IL Department: Clinical Research Apply To This Job Email This Job Return To List Job Description * * * Participate in the site nomination process; perform evaluation of site capability to deliver the contractually agreed to number of patients and high quality data then make recommendation for inclusion in the clinical trial. > Assume ambassadorial role to facilitate communication between sites and Novartis line functions to increase value proposition to investigators. > Facilitate preparation and collection of site level documents. > Execute site initiation and training activities. > Perform monitoring visits according to monitoring plan and author study monitoring reports. > Manage site drug supply management. > Resolve site level update of technical systems (ClinAdmin, EDC). > Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc).           Fewer «

Nashville Based Regional CRA - 431627 Company: ConsignMed Job#: 1051 Positions: 1 Job Type: Full Time - Contract Location: ......  More »    Fewer «   Nashville - TN Department: Clinical Research Apply To This Job Email This Job Return To List Job Description * * * Nashville based CRA Travel at least 50% Seasoned Regional CRA experience required. Please include city/state on resume Manager would consider a strong Coordinator with Oncology experience Delivery of high quality data according to agreed timelines and budget, ensuring adherence to international and local regulations and Novartis SOP standards. Demonstrate exceptional customer focus as evidenced by positive feedback from Novartis colleagues and external customers (Investigators). Participate in the site nomination process; perform evaluation of site capability to deliver the contractually agreed to number of patients and high quality data then make recommendation for inclusion in the clinical trial.           Fewer «

Regional CRA for immediate need. Must have Womens Health experience. .As key team members supporting new drug applications ......  More »    Fewer «  , the Regional CRA is accountable for on-site clinical monitoring activities from study start-up through close-out. As specified in the monitoring plans, the RCRA will perform source document verification review of Case Report Forms, oversee drug accountability, as well as manage investigational site to ensure compliance with FDA regulations, ICHGCP guidelines, and company SOPs. Requirements Travel These positions are home-based and require over 50 travel Experience For you to be the successful candidate we are looking for in these roles you must have a proven track record of monitoring clinical trials in a variety of Therapeutic Areas through the CRO or Pharmaceutical industry Education For consideration, you must hold a Bachelors degree, preferably in a scientific or nursing discipline Due to the precise requirements of these positions           Fewer «

Permanent Regional Home-based CRA position available across the United States Company is requiring previous experience ......  More »    Fewer «   working in Cardiovascular and Device trials. You MUST have BOTH of these therapeutic areas to qualify. Need to have at least 2 years home-based experience and 3 years monitoring multiple sites Bachelors Degree is required You must be located within 30 miles or an international airport **If you meet these requirements, please contact me at your earliest convenience to setup a phone screen.           Fewer «

Currently, one of our top clients is in search of an exceptional Regional Clinical Research Associate located in Cleveland ......  More »    Fewer «  , Ohio. The Regional CRA will be responsible for conducting all clinical site activities according to the monitoring plan and in accordance with the study timelines and company objectives. This includes but is not limited to:Manage the activities of clinical investigative sites           Fewer «

Currently, one of our top clients is in search of an exceptional Regional Clinical Research Associate located in ......  More »    Fewer «   Indianapolis, Indiana. The Regional CRA will be responsible for conducting all clinical site activities according to the monitoring plan and in accordance with the study timelines and company objectives. This includes but is not limited to: * Manage the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas with the ability to manage, with minimal supervision, sites participating in more complex clinical studies and/or sites requiring more oversight of operational issues * Manage the overall activities of site personnel over whom there is no direct authority and motivate/influence them to meet study objectives * Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel           Fewer «

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional ......  More »    Fewer «   development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you. This allows you to stay just as dedicated and still strike a balance between work and home. Currently, one of our top clients is in search of an exceptional Regional Clinical Research Associate located in Cleveland, OH. The Regional CRA provides site management and clinical monitoring for assigned clinical studies, assuring compliance with GCP/ICH and study objectives. Specific Accountabilities:           Fewer «

Send this job to a friend See all Kforce Professional Staffing opportunities Status: Temporary/Contract/Project Level: ......  More »    Fewer «   Experienced (Non-Manager) Job Location: Birmingham, AL Job Ref Code: 1300~NRC~998767T1 About Kforce . . . . . . . . . . . . . Kforce Clinical Research offers more than 20 years of experience with a strong commitment to providing exceptional service by building great teams dedicated to operational excellence. Kforceâs long-term client relationships open the door to rewarding opportunities, giving candidates access to the worldâs top biopharmaceutical companies. In addition to providing exciting opportunities, our Firm takes the time to get to know each candidateâs career aspirations, enabling Kforce to be their career advocate. Our clinical research specialty areas include: monitoring/site management, study management, regulatory affairs, drug safety, data management, data entry, clinical programming, biostatistics and quality assurance.           Fewer «

A Large Clinical Research Organization is searching for an immediate Clinical Research Associate-Contract (CRA) based in the ......  More »    Fewer «   East Coast area. The following experience and expertise are required. Project Details: Study/Therapeutic Area: Oncology (Solid Tumor) Region: East Coast Contract = Yes (Door to Door Travel Payment) Phase:III Travel: 60% Homebased? Yes Allocation Required: 100% Full-time Monitoring Responsibilities will include: -Preparing and distributing case report forms (CRF), study reference manuals, and monitoring guidelines/manuals. -Modifying and developing Case Report Forms (CRF's) -Participating in investigator meetings. -Site selection, initiation, interim and closeout. -Managing Institutional Review Board (IRB) and informed consent issues as well as participating in investigator recruitment and site selection visits. -Collecting and verifying essential regulatory documents, and site personnel training.           Fewer «

A Large Clinical Research Organization is searching for an immediate Clinical Research Associate-Contract (CRA) based in the ......  More »    Fewer «   East Coast area. The following experience and expertise are required. Project Details: Study/Therapeutic Area: Oncology (Solid Tumor) Region: East Coast Phase:III Travel: 60% Homebased? Yes Allocation Required: 100% Full-time Monitoring Responsibilities will include: -Preparing and distributing case report forms (CRF), study reference manuals, and monitoring guidelines/manuals. -Modifying and developing Case Report Forms (CRF's) -Participating in investigator meetings. -Site selection, initiation, interim and closeout. -Managing Institutional Review Board (IRB) and informed consent issues as well as participating in investigator recruitment and site selection visits. -Collecting and verifying essential regulatory documents, and site personnel training. -Conducting periodic monitoring activities with the investigative sites, including reviewing case report forms (CRF).           Fewer «

A Large Clinical Research Organization is searching for an immediate Clinical Research Associate-Contract (CRA) based in the ......  More »    Fewer «   East Coast area. The following experience and expertise are required. Project Details: Study/Therapeutic Area: Oncology (Solid Tumor) Region: East Coast Contract = Yes (Door to Door Travel Payment) Phase:III Travel: 60% Homebased? Yes Allocation Required: 100% Full-time Monitoring Responsibilities will include: -Preparing and distributing case report forms (CRF), study reference manuals, and monitoring guidelines/manuals. -Modifying and developing Case Report Forms (CRF's) -Participating in investigator meetings. -Site selection, initiation, interim and closeout. -Managing Institutional Review Board (IRB) and informed consent issues as well as participating in investigator recruitment and site selection visits. -Collecting and verifying essential regulatory documents, and site personnel training.           Fewer «

The Qualified Candidate Will Possess: -3-4 yrs+ of on-site clinical trial monitoring --1-2 yrs+ CNS/Oncology/ or Infectious ......  More »    Fewer «   Disease Therapeutic background as a monitor --Bachelors or higher degree mandatory in Life or Health Science (RN or medical background is a plus) -Preferred Nursing Background --SOPs, FDA, and GCP regulations and practices --Strong working knowledge of guidelines, and systems for clinical trial management --Excellent interpersonal, verbal, and written communication skills --Attention to detail and strong organizational skills Required Skills for Regional CRA Job: CRA REGIONAL MONITORING CLINICAL RESEARCH ASSOCIATE GCP CLINICAL RESEARCH OTHER:NO relocation assistance available for this position Join Aerotek Scientific LLC(SM), one of the fastest growing providers of scientific and clinical research services in the nation.           Fewer «

Our client, located in Chicago, IL is seeking a Sr. CRA for an immediate contract position. Details include: Responsible for ......  More »    Fewer «   performing study site management activities regarding the implementation, monitoring, and summarization of clinical trials to ensure adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Develop and maintain collaborative working relationships with clinical investigative sites. Reports to the Senior Regional Manager/Regional Manager, Field Trial Operations. Receives direction on individual clinical studies by the Site Management Lead, Project Manager and Clinician responsible for that project. Other internal relationships include other functional groups within CTO. External relationships are with clinical investigative sites. * Serves as the primary contact for clinical investigative sites on multi-therapeutic trials.           Fewer «

Job: IRC107133 Description Position Summary: · Design and implement internal and external communications strategy ......  More »    Fewer «  , including, but not limited to: marketing, public relations and community involvement strategies in partnership with all regional lines of business and consistent with overall regional business strategy. Ensure partnership with corporate community development/CRA objectives/teammates. · Assist in designing regional business strategy as member of regional senior leadership team with focus on internal and external communications. · In coordination with Regional President, create strategic partnerships and maintain visibility with top decision makers/influential organizations within the community on behalf of Huntington. Identify appropriate matches for Huntington financial investment and Huntington colleague board involvement within influential community organizations.           Fewer «

One of Aerotek's clients a fast growing CRO company is looking to bring on a Home-Based Lead Clinical Research Associate to ......  More »    Fewer «   join their team. The ideal candidate will have 3-4 years experience in Clinical Research. This company is based in the Midwest. Some of the job responsibilities are as follow: -Helping out Clinical operations group get monitoring set up. -Lead CRA will be involved in going on monitoring visits. -Previous experience Regional Monitoring. -Working with Clinical Research Associates to make sure that they are performing well. -Less than 10% Travel. Join Aerotek Scientific LLC(SM), one of the fastest growing providers of scientific and clinical research services in the nation. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across the scientific and clinical research communities.           Fewer «

One of Aerotek's clients a fast growing CRO company is looking to bring on a Home-Based Lead Clinical Research Associate to ......  More »    Fewer «   join their team. The ideal candidate will have 3-4 years experience in Clinical Research. This company is based in the Midwest. Some of the job responsibilities are as follow: -Helping out Clinical operations group get monitoring set up. -Lead CRA will be involved in going on monitoring visits. -Previous experience Regional Monitoring. -Working with Clinical Research Associates to make sure that they are performing well. -Less than 10% Travel. Join Aerotek Scientific LLC(SM), one of the fastest growing providers of scientific and clinical research services in the nation. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across the scientific and clinical research communities.           Fewer «

Job Code Description: Regional Commercial RE Sales Manager - 66959 Job Purpose/Mandate: At our company, we have been ......  More »    Fewer «   helping our customers and communities for over 125 years. Working with us means being part of a team of talented, passionate individuals with a shared focus on working together to deliver great customer experiences. We stand behind your success with the support you need to turn your potential into performance. Harris is committed to an inclusive, equitable and accessible workplace. We are an Equal Opportunity Employer. By embracing diversity, we gain strength through our people and our perspectives. This position is responsible for championing the affordable housing finance and some commercial real estate sales management leadership elements throughout the organization. Serves as a member of the management team with direct responsibility for the development and risk management of commercial real estate related relationships; deposits and loans.           Fewer «

Job Code Description: Regional Commercial RE Sales Manager - 66959 Job Purpose/Mandate: At our company, we have been ......  More »    Fewer «   helping our customers and communities for over 125 years. Working with us means being part of a team of talented, passionate individuals with a shared focus on working together to deliver great customer experiences. We stand behind your success with the support you need to turn your potential into performance. Harris is committed to an inclusive, equitable and accessible workplace. We are an Equal Opportunity Employer. By embracing diversity, we gain strength through our people and our perspectives. This position is responsible for championing the affordable housing finance and some commercial real estate sales management leadership elements throughout the organization. Serves as a member of the management team with direct responsibility for the development and risk management of commercial real estate related relationships; deposits and loans.           Fewer «