better Biotech Pharma Job in Texas

Our client is searching for two Nurse Clinical Research Coordinators to support a study in San Antonio. Candidates will be responsible to perform clinical research and patient treatment in conjunction with one or more protocols. Responsibilities: 1. Interviews patients for protocols and collects and analyzes appropriate data for recruitment purposes, determine patient commitment and obtains informed consent. 2. Reviews new patient records and screens patients for eligibility for participating in research

Our client is searching for a Clinical Research Assistant for a project in San Antonio. The candidate will be responsible to monitor the execution of clinical trials associated with specific projects and to ensure that all necessary steps are being taken. Responsibilities: 1. Ensures that regulatory documents are maintained and are up to date. 2. Ensures that all adverse events have been documented and forwarded to the appropriate principal investigator. 3. Reviews Case Report Forms for patient eligibility

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional 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 position is open as of 10/17/2009. Clinical Research Coordinator - Pharmaceutical CRO - San Antonio Clinical Research Coordinator - Pharmaceutical CRO - San Antonio We offer a full range of clinical research services. We provide expert advice on everything from protocol development to regulatory submission. Our two modern clinical research facilities in Austin (100 beds) and San Antonio (250 beds) offer a full range of clinical research services. Responsibilities: Assure that the integrity and

Clinical Research Analyst Job Category: Managerial/Professional Sub Category: Research Department: Gynecologic Oncology Salary:SALARY_LOW=0; SALARY_LOW=46800.00; if(SALARY_LOW==0) document.write('Not Available'); else document.write('$46800.00 - $70200.00'); Employment Status: Full Time Work Week: Mon-Fri Shift: Days SUMMARY The primary purpose of the Clinical Research Analyst is to provide strategic planning and administration of payment monitoring for research studies sponsored by private industry

Clinical Research Program Coordinator Job Category: Research Sub Category: Professional Department: Gynecologic Oncology Salary:SALARY_LOW=0; SALARY_LOW=46000.00; if(SALARY_LOW==0) document.write('Not Available'); else document.write('$46000.00 - $69000.00'); Employment Status: Full Time Work Week: Mon-Fri Shift: Days Function: Provides administrative and patient care services for the coordination of clinical research activities for the Clinical Cancer Genetics Program. Scope: Coordinates clinical research

ClinForce is currently seeking a Clinical Research Coordinator - CRC for Whitney, TX. Successful candidate will be responsible for the following: - Work directly with patient/subject interface at investigational sites to deliver high quality patient data in accordance with regulations and as required by the study protocol. - Participate in the recruitment and screening of research participants. - Design and maintain organizational tools to conduct the research study accurately in compliance with

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional 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

POSITION SUMMARY: The Clinical Data Coordinator (CDC) will assist in the planning, implementation, conduct and reporting of the Data Management portion of clinical trials as a member of clinical trial study teams per Department SOPs, guidelines and GCP. The CDC will work with the Supervisor and Study Lead to develop/execute technical Data Management responsibilities. DUTIES AND RESPONSIBILITIES (essential functions of position): Nothing in this job description restricts management s right to assign

Independent retail pharmacy in South Dallas needs Full-Time Pharmacist. Experience in retail pharmacy and experience in compounding as well as computer knowledge and outstanding customer service skills. Responsible for the daily clinical and customer service operations of the pharmacy including prescription dispensing and patient education. Paid Vacation, Holidays, & Sick Leave Excellent Salary Current B.S. Pharmacy or Pharm. D and TX Pharmaceutical license required At least 1 yr. exp of retail

This position will act as lead statistician on projects of moderate to large size and complexity; will support lead statistician on very large, complex studies. May have staff management and/or project management responsibilities. Responsibilities may include: - Leading a project team. This involves conducting team meetings, maintaining project timelines, assessing resources needed, providing resources, and preparing the budget. Ensure that Standard Operating Procedures are being followed and that appropriate

Job Summary The Director of Clinical Research is responsible for all clinical research operations at WellMed. It is the responsibility of the Director to plan and steer all activities required to attain corporate and departmental goals. Essential Job Functions 1. Develop short and long term departmental goals in accordance with corporate goals for growth and expansion. 2. Develop short and long term strategic plans to assure the maintenance and growth of the research department. 3. Develop

This position will act as lead statistician on projects of moderate to large size and complexity; will support lead statistician on very large, complex studies. May have staff management and/or project management responsibilities. Responsibilities may include: - Leading a project team. This involves conducting team meetings, maintaining project timelines, assessing resources needed, providing resources, and preparing the budget. Ensure that Standard Operating Procedures are being followed and that appropriate

Clinical Research Coordinator Description: - Responsible for procuring, maintaining, and assuring protocol compliance for all patients on clinical trials. - Collaborates with physician in determining eligibility of patients for clinical trials. - Provides education for staff and patients. - Ensures site research quality by practicing in compliance with Corporate Policy and Procedures, ICH principles of Good Clinical Practice and applicable federal, state, and local regulations. -

Equal Employment Opportunity The University of Texas Medical Branch at Galveston is an equal...

Job Requirements Job Requirements and Compensation Prefer experienced LVN or RN with Texas License...

collection Equal Employment Opportunity The University of Texas Medical Branch at Galveston is an equal...

Clinical Staff Pharmacist Location: TX-Sugar Land Department: St. Luke's Sugar Land Hospital ID: 934 # of openings: 1 Description Per Diem Clinical Staff Pharmacist St. Luke s Sugar Land Hospital / Sugar Land, TX Description:You will interpret, evaluate, compound, and dispense medications according to written orders issued by an authorized prescriber. You will also identify, prevent, assess and resolve medication-related problems to ensure a safe and optimal patient outcome; and promote, through criteria-based

Location San Antonio Texas Austin Texas Want to interview today...

is preferred Country USA State Province Region Texas Site Location Field Research Employer of Choice...

Clinical Staff Pharmacist Location: TX-Huntsville Department: Huntsville Memorial Hospital ID: 932 # of openings: 1 Description Clinical Staff Pharmacist - Full Time Huntsville Memorial Hospital, Huntsville, TX Description:You ll fill orders with accuracy; check technician prepared products before release; maintain security of pharmacy and controlled substances; enter orders and patient information with accuracy; aid in the training of new staff; update the Director about the daily activities of the pharmacy

Clinical Research Associate H/O Department: CCHS H/O Program Supp. Schedule: Full-Time Shift: Days Hours: varies HR Use Only: CB- 10/21/09 Job Details: Summary: Responsible for coordinating the use of cooperative group studies within the Hematology and Oncology Center. He/She will facilitate the initiation and maintenance of the protocol, determine eligibility, register patients on study, as well as ensure that complete and accurate data are collected and maintained for all patients on study or undergoing

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. OptumHealth is part of the family of companies that make UnitedHealth Group one of the leaders across most major segments of the US health care system. If you want more meaning in your career - as a clinician or a business

experience Equal Employment Opportunity The University of Texas Medical Branch at Galveston is an equal...

preferred Equal Employment Opportunity The University of Texas Medical Branch at Galveston is an equal...

DIRECT HIRE Clinical Research Coordinator (CRC) Opportunity! Currently available: A Full Time, DIRECT HIRE Clinical Research Coordinator (CRC) opportunity at a growing CRO located in the San Antonio, TX area! Award winning benefits package includes 401K performance incentive plan, and childcare reimbursement. Please see below for more details! Responsibilities: - Will review study protocol and investigator's brochure for studies they will be assigned to. - Will attend the investigator's meeting, pre-study

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. OptumHealth is part of the family of companies that make UnitedHealth Group one of the leaders across most major segments of the US health care system. If you want more meaning in your career - as a clinician or a business

Wilford Hall Medical Center in San Antonio Texas...

- The Henry M. Jackson Foundation (HJF) is seeking a Clinical Research Assistant for the Infectious Disease Clinical Research Program (IDCRP)located at the Brooke Army MedicalCenter and WilfordHallMedicalCenter located in San Antonio, TX. HJF provides administrative and management support to IDCRP. The IDCRP is a collaborative research effort with the National Institute of Allergy and Infectious Diseases (NIAID). Established at USUHS in 2005, this unique program aims to strengthen infectious disease clinical

Clinical Staff Pharmacist - Full Time Huntsville Memorial Hospital, Huntsville, TX Description: You ll fill orders with accuracy; check technician prepared products before release; maintain security of pharmacy and controlled substances; enter orders and patient information with accuracy; aid in the training of new staff; update the Director about the daily activities of the pharmacy; and aid the Director in maintaining the pharmacy. This position is 40 hours per week, working a combination of days and

Clinical Staff Pharmacist - Full Time Huntsville Memorial Hospital, Huntsville, TX Description: You ll fill orders with accuracy; check technician prepared products before release; maintain security of pharmacy and controlled substances; enter orders and patient information with accuracy; aid in the training of new staff; update the Director about the daily activities of the pharmacy; and aid the Director in maintaining the pharmacy. This position is 40 hours per week, working a combination of days and

Inventiv Clinical Solutions is looking for a CRA II to join their team Can be located in any of the following locations: -Dallas, TX -Chicago, IL -Denver, CO -Cincinnati, OH -Indianapolis, IN -Atlanta, GA Responsibilities: - Serve as a liaison between clinical trial sponsor(s) and sites - Conduct site qualification, initiation, monitoring and close-out visits of moderate to complex clinical studies according to regulatory standards, SOPs and contract requirements - Identify, evaluate and recommend

At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance s impressive history of company stability and growth. We ve achieved these results by fostering a work environment that encourages, develops and leverages our team s capabilities. Covance s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! As the Clinical

At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance s impressive history of company stability and growth. We ve achieved these results by fostering a work environment that encourages, develops and leverages our team s capabilities. Covance s ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! As the Clinical

Clinical Staff Pharmacist Job Code: 21867 Facility: Doctors Hospital of Laredo Location: LAREDO, TX US Travel Involved: None Job Type: Full Time Job Level: Experienced (Non-Manager) Minimum Education Required: Bachelor's Degree Skills: Health Care ->Pharmacy Category: Professionals FTE: 1.00 Position Summary: Process orders for parenteral and enteral medications, and other pharmaceuticals as needed for optimal patient care according to standards and practices for patients in all age groups including neonatal

SUMMARY The primary purpose of the Clinical Research Analyst is to provide strategic planning and administration of payment monitoring for research studies sponsored by private industry, foundations, and federal agencies for the Department of Gynecologic Oncology. SCOPE: Responsible for the financial management and oversight of all research protocol contracts. Assists faculty and Principal Investigators with the development and negotiation of financially appropriate contracts and budgets for research protocols

At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional 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

Clinical Research Coordinator, Clinical Operations At ICON it's our people that set us apart. ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I - IV clinical studies. ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract

Clinical Research Coordinator, Clinical Operations At ICON it's our people that set us apart. ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development - from compound selection to Phase I - IV clinical studies. ICON enjoys a strong reputation for quality and is focused on staff development. We make it our

THIS POSITION IS LOCATED IN SAN PEDRO, CA RELOCATION IS REQUIRED Shift: 4 - Rotating/Variable Shift Department: SPH PHARMACY Employee Status: On Call Providence Little Company of Mary Medical Center San Pedro is a 259-bed nonprofit hospital that has served the Harbor and greater South Bay communities since 1925. The hospital is co-operated by the sisters of Little Company of Mary and the Sisters of Providence. Little Company of Mary - San Pedro was named one of the nation's Top 100 Performance Improvement

THIS POSITION IS LOCATED IN TORRANCE, CA RELOCATION IS REQUIRED Shift: 4 - Rotating/Variable Shift Department: LCMH PHARMACY Employee Status: Full-Time Little Company of Mary Hospital Torrance has served the South Bay communities for more than 40 years and today boasts a reputation for clinical excellence andas a highly regarded emergency healthcare designation. The 434-bed hospital is known for specialties including cardiovascular services, women's and children's health, oncology and is at the forefront

Staff/Clinical Pharmacist - Nights Kaye/Bassman International has been engaged by a 250 bed, suburban hospital in Northern Colorado to locate a Staff/Clinical Pharmacist for a new position. This beautiful, financially sound Medical Center provides the surrounding communities with a number of medical specialties ranging from comprehensive cardiac and trauma care to family-based primary care services. The Director of Pharmacy is willing to train and mentor motivated pharmacists looking for more clinical exposure

Clinical Staff Pharmacist PRN Location: TX-San Antonio, 78240 Department: Foundation Surgical Hospital ID: 899 # of openings: 1 Description Comprehensive Pharmacy Servicesis the nation's leading independent pharmacy management service provider to acute care hospitals and behavioral systems, delivering pharmacy service value through financial, operational, clinical, therapeutic, and regulatory expertise. CPS has outstanding opportunities for pharmacists in the areas of dispensing, clinical and administrative

Chiltern International is a well established global contract research organization with offices throughout Europe, North America and India. We were established in 1982 and have served pharmaceutical, biotechnology, and device companies in over 38 countries worldwide. Due to our continued growth, Chiltern is seeking a highly motivated individual to join us as a Senior Clinical Research Associate. SUMMARY OF POSITION: The SCRA is a high-profile role within the Department, using their experience as a knowledge

PerDiem Clinical Staff Pharmacist weekends Texas Regional Medical Center Sunnyvale TX Description You...a hospital setting or residency preferred Facility Texas Regional Medical Center is a brand new...

PerDiem Clinical Staff Pharmacist weekends Texas Regional Medical Center Sunnyvale TX Description You...a hospital setting or residency preferred Facility Texas Regional Medical Center is a brand new...

Business Title Clinical Research Manager - RN Requisition ID 17655BR Job Category Clinical Research Locations USA - Dallas, TX Shift 1 Job Posting At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance's impressive history of company stability and growth. We've achieved these results by fostering a work environment that encourages, develops and leverages our team's capabilities. Covance

Supervisor, Clinical Research Scope - Under limited supervision, is responsible for enlisting and maintaining patients on research protocol regimens. - Collaborates with physician in determining eligibility of patients for clinical trials. - Provides education to staff and patients. - Ensures proper treatment and assumes responsibility for clinical documentation for patients on protocol. - Practices in compliance with principles of Good Clinical Practice and applicable federal, state

Sr Biostatistician I- Clinical Trials Job ID: CJF20090408-10830 Description: The incumbent will provide statistical and technical expertise in support of R&D pipeline objectives. They will be responsible for providing timely and accurate expert-level support for clinical study design, analysis plan preparation, statistical analysis, and interpretation of clinical study results. Responsibilities also include coordination of Biostatistics support with Clinical Trial Management and other functional units

Manager Biostatistics - Medical Devices Job ID: WP20093108-10935 Description: Plans, directs, and coordinates activities of Biostatistics in one or more therapeutic areas to ensure that aims, goals, and specified objectives are accomplished in accordance with prescribed priorities, time limitations, and funding conditions. Acts as an advisor to subordinate staff members, the SAS programming group, and Clinical Data Management to help ensure that R&D objectives are met according to established schedules