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AE CASE MANAGEMENT Receipt Execute receipt of Drug Safety phone calls and complete telephone AE form Create phone call communication logs in ARISg Triage Support the triage of cases conducted by Snr Specialist as needed Assessment - Complex Case Support the assessment of complex cases conducted by Snr Specialist as needed Assessment - Non-Complex Case Execute QC on key fields of serious cases Create key fields updates in ARISg based on QC, as needed Execute case assessment (review events, determine labeledness

Our client, a clinical research firm, is actively seeking a Clinical Research Coordinator for their Tidewater area facilities. Clinical Research Coordinators will be responsible for: -Coordinating and implementing an approved research study according to protocols and policies -Working with physicians, clinical nurses and patients in the selection of and participation by appropriate patients. -Collecting and analyzing data for healthcare professionals -Monitoring study as required -Evaluating patients responses

Our client, a fast-growing CRO located in Midtown Manhattan is in need of a Clinical Research Coordinator. This is an immediate opening and a great opportunity for a Coordinator to get experience within a CRO and work in NYC. The Clinical Research Coordinator will be responsible for managing the coordination for several Phase I clinical trials. The CRC will be responsible for developing site documentation, collecting data, and study subject recruitment. The CRC will be responsible for enrolling and consenting

The primary purpose of this position is to receive and process adverse event information from clinical trials and spontaneous reports. These reports come from physicians and other health care providers, the clinical research department, subsidiaries, legal, etc. The specialist supervises the information coordinator in the entry of the data into the computerized database. The job requires the synthesis of the event into a cogent medical narrative summary and the evaluation and entry of the data into proprietary

A CRO has an immediate need for an experienced Regional Clinical Research Associate. This Regional Clinical Research Associate will be home-based and cover sites on the West Coast for a Post-Marketing Study. The initial contract is for 1 year and can be extended. Major job duties include: - Monitoring multiple clinical research sites. - Follow up with sites via phone and e-mail. - Responsible for managing regulatory site documents and binders. - Training of site staff. - Communicate with in-house CRO staff as

Our client in Frederick, MD develops and delivers Vaccines and related products and are an experienced in the advanced development of bio defense biologics, including live attenuated vaccines, recombinant vaccines, therapeutics, therapeutic polyclonal antibodies, and alternative vaccine delivery systems. Job Duties: CRA performing in-house duties including... -Assisting clinical project manager(s) in the management and coordination of assigned clinical research studies, in compliance with FDA regulations, ICH

Job Advertised by Pharmadiversity Job Board - Data Managers Are YOU Ready To Make A Global Impact?? Welcome to Covance! Since 1986, Covance Central Laboratory Services has been the world's leading provider of clinical trial laboratory services, dedicated to testing specimens and resulting and reporting data. We manage over a third of all clinical trials conducted in the world, have experience in over 100 countries, and service six continents. We are currently looking for a Data Manager to join our Indianapolis

Job Advertised by Pharmadiversity Job Board - Immediate Travel Position Available! Clinical Pharmacist Travel Job Hospital Shift: Days State License: IN Certifications: BLS/CPR, ACLS On Call requirements: No call Weekend requirements: No rotation. 1-2 years experience Start ASAP Medical Connections offers nationwide travel opportunities in a variety of settings; from skilled nursing to hospitals, outpatient and inpatient facilities that allow us to find you a travel assignment

Review incident reports and determine if any results are unfavorable or abnormal. Document results that may include negative reaction to the drug or a negative interaction with the other drugs. Specific qualifications: : Responsible for the telephone and written communication with physicians, other health-care professionals, Sales personnel, and patients, in response to spontaneous and clinical trial Adverse Drug Reactions, Medical Devices Experiences, and technical reports associated with company products

A pharmaceutical company has an opening for an In-House Clinical Research Associate in Beltsville, Maryland. JOB DUTIES INCLUDE: -Ensure compliance with appropriate SOPs. -Support Management in meeting company milestones. -Participate in regular meetings. -Coordinate/schedule internal and external meetings. -Track/update study activities, including: CRA monitoring visits, site monitoring visit reports. -Process Serious Adverse Experience Reports. JOB QUALIFICATIONS INCLUDE: -1-2 years of Clinical Documentation

Our client, a leader in healthcare information services, is looking for a Clinical Research Associate. This person will be responsible for all aspects of study initiation, including coordinating with various departments to ensure a smooth start-up. Additional responsibilities: - Presenting professional presentations at meetings - Monitoring sites and preparing reports for sponsor - Work with QA for study specifications - Review reports and release to sites - Traveling to investigator meetings This position will

My client a medium size biopharmaceutical company is looking for an In House CRA. The CRA is assist in the preparation for an NDA submission. This position involves the ability to recognize and locate study related ICH essential documents within the company's document management system and in official paper files. My client is looking for someone who is familiar with data management and or statistical documents and data would be a plus. Knowledgeable with FDA/GCP/ICH guidelines and phase 1-3 clinical trial

A CRO has an immediate need for an experienced Regional Clinical Research Associate. This Regional Clinical Research Associate will be home-based and cover sites on the West Coast for a Post-Marketing Study. The initial contract is for 1 year and can be extended. Major job duties include: - Monitoring multiple clinical research sites. - Follow up with sites via phone and e-mail. - Responsible for managing regulatory site documents and binders. - Training of site staff. - Communicate with in-house CRO staff as

Our client, a fast growing pharmaceutical company is in need of a Clinical Data Manager. They would like someone to join their team full-time as a partner for their Data Management team. The right candidate will manage all aspects of data collection within a specific disease area. They will also: -Generate queries for missing and/or discrepant data -Review sections of study protocols related to patient treatment, supportive care, specimen submission, patient follow-up, and any other sections requiring understanding

A CRO has an immediate need for an experienced Regional Clinical Research Associate. This Regional Clinical Research Associate will be home-based and cover sites on the West Coast for a Post-Marketing Study. The initial contract is for 1 year and can be extended. Major job duties include: - Monitoring multiple clinical research sites. - Follow up with sites via phone and e-mail. - Responsible for managing regulatory site documents and binders. - Training of site staff. - Communicate with in-house CRO staff as

An outstanding opportunity to work at Fresenius Medical Care North America. Fresenius is the world's largest, integrated provider of products and services for individuals with chronic kidney failure, a condition that affects more than 1,300,000 individuals worldwide. Through its network of over 49,000 employees in over 100 countries, FMCNA offers outstanding career opportunities across the globe in a rapidly expanding yet stable environment . Working at Fresenius means growing your career while making a difference

Company Name: Provena United Samaritans Medical Center Employment Type: Full Time (Exempt) Department: Pharmacy Salary: Highly Competitive Shift/Hours: 8 hours/day Shift Details: primarily to rotate first and second shift. Occasional rotate 3rd shift Hours/Pay Period: 80 Degree Required: None Specified Job ID: 2008.63700.1955 Date Posted: Sep 25, 2008 Years Experience: unspecified Job Class: Professional/Leadership Note: Please read the complete description below before applying for

- The pharmacist assures appropriate selection, dosing, administration, and monitoring of medication orders. Graduate from a College of Pharmacy accredited by the American Council on Pharmaceutical Education (ACPE). One year Pharmacist experience in hospital setting preferred. Licensure: Licensed as a Pharmacist(D.Ph) in the State of Tennessee. ~cb~ Hours: 9p - 7a Shift: 7on/7off

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 of information

POSITION SUMMARY: The Clinical Data Manager is responsible for processing and reviewing data for all clinical trials. ESSENTIAL DUTIES AND RESPONSIBILITIES: - Coordinate the printing, shipping and receipt of CRFs in multiple studies/sites/countries. - Process, review, and query clinical trial data using Oracle Clinical database. - Generate, track, and resolve data queries using data clarification forms (DCFs). - Perform review of CRFs, issue manual queries as needed, and maintain archiving of CRFs in house

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and develop

Job Classification: Contract Description: A Pharmaceutical company has an immediate opening for an experienced Clinical Data Manager in North Chicago, Illinois. The Clinical Data Manager 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. Job Duties Include: -Provides accurate data acquisition to statistical

Job Classification: Contract Description: A Pharmaceutical company has an immediate opening for a Senior Clinical Research Associate in North Chicago, Illinois. The Senior Clinical Research Associate is responsible for conducting Phase I-IV studies according to Federal Regulations and ICH guidelines and study protocol. Job Duties Include: -Responsible for training sites on protocol related issues. -Home-Based Regional Travel 35-40%. -Writing study protocols. -Designing CRFs, CRO selection, CRO training

Job Classification: Contract Description: A Pharmaceutical company has an immediate opening for a Jr-level Clinical Research Associate with a good attitude in North Chicago, Illinois. The Clinical Research Associate is responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines and study protocol. Job Duties Include: -Responsible for training sites on protocol related issues. -Home-Based Regional Travel 20%. -Assisting staff in planning study

Shift: 4 - Rotating/Variable Shift Department: LCMH PHARMACY Employment Status: On Call Providence Little Company of Mary Hospital, located in Torrance, CA is a 300+ bed facility which provides premier healthcare to the Southbay area. We currently have an on-call pharmacist, variable shift position available. I. POSITION SUMMARY The Clinical Pharmacist is a registered pharmacist who is responsible for ensuring the safe and appropriate use of drugs. Fullfillment of this responsibility is

Success through teamwork We work together to find a better way and break new ground to make progress possible. Focused on common goals, we raise the standard and make a difference. We strive for excellence in everything we do. At ICON, career possibilities can become realities for those who look for challenges and embrace learning and growth opportunities. ICON Clinical Research is dedicated to providing the pharmaceutical and biotechnology industries with exceptional clinical research and biometrics services

Senior Clinical Data Manager MUST BE WORKING FOR A PHARMA COMPANY & NO JOB HOPPERS PLEASE. LOCAL IS BEST BUT WE WILL RELO IF NECESSARY. Our client is a leading global biotechnology company unlocking the potential of molecular discovery and advancing the practice of medicine. The company provides molecular and pharmacogenomics services, as well as clinical diagnostics for the improvement of patient care with headquarters in Newton, Massachusetts and operations in Texas, Connecticut, RTP - North Carolina

How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Support projects and functions throughout Research & Development, including compound selection, exploratory clinical development, and late development, with decision analysis and statistical modeling. - Integrate information, opinion, and data regarding drug efficacy, safety, and market conditions to evaluate

How do you spend your day? Are you passionate about what you do? At Novartis, our focus is clear, our purpose defined. We're part of a team that's making a difference in the quality of people's lives. Support projects and functions throughout Research & Development, including compound selection, exploratory clinical development, and late development, with model-based planning, clinical trial design, evaluations, integrated analysis, and reporting. Support decision-making by pre-clinical or clinical teams with

Clinical Research Coordinator - Dallas Clinical Research Coordinator - Dallas Summary Texas Oncology Cancer Center at Presbyterian Hosp[ital of Dallas, in Dallas, Texas has an exciting opportunity for a Clinical Research Coordinator. This is a full time position for an experienced oncology research nurse in a growing, state of the art, medical oncology practice. Excellent salary and benefits included. Responsibilities of Clinical Research Coordinator - Dallas - Screens potential patients for protocol

Job Classification: Direct Hire Description: Our client, a fast-growing CRO located in Midtown Manhattan is in need of a Clinical Research Coordinator. This is an immediate opening and a great opportunity for a Coordinator to get experience within a CRO and work in NYC. The Clinical Research Coordinator will be responsible for managing the coordination for several Phase I clinical trials. The CRC will be responsible for developing site documentation, collecting data, and study subject recruitment. The

Our client is currently hiring for the following position: Clinical Pharmacist (Organ Transplant) Position Details: Establishes and coordinates the department's clinical services for patients. Will work with physicians in developing and assessing new programs. Participates in the department's teaching/training activities and conducts research.. Job Requirements: Minimum Qualifications: - Doctor of Pharmacy from an accredited School of Pharmacy (or equivalent experience). - Current licensure

Our client is currently hiring for the following position: Clinical Pharmacist (Infectious Diseases) Position Details: Establishes and coordinates the department's clinical services for patients. Will work with physicians in developing and assessing new programs. Participates in the department's teaching/training activities and conducts research. - Participation in the facility's Antibiotic Utilization Subcommittee - Participation in antimicrobial tracking and quality improvement initiatives

Job Title: Clinical Research Coordinator- Cardiovascular Portfolio Job Category: Professional/ Technical Hours per Shift: 8 Shift Start Time: 8 Shift End Time: 5 FTE: 1.0 Shift: 1st Company: WFH-Corporate Services-9001 Department: Research State: Wisconsin City: Wauwatosa Location: Wisconsin Heart Hospital - 10000 W. Blue Mound Rd Requirements: RN Preferred but will consider an LPN 3-4 years Externally funded clinical research experience preferred Excellent communication skills Entrepreneurial spirit Solutions

Job Summary For assigned studies, provides oversight and support to clinical operations team in planning, conduct, and closeout of assigned clinical studies assuring consistency across regions and compliance with GCP/ICH and study objectives. Provides sponsor oversight of clinical monitoring activities including site initiation and management, document management, study training, safety reporting, and oversight of regional leads and field CRAs including management of trip report review and issue resolution

-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

Aerotek is currently looking for a qualified candidate that will serve as a lead Biostatistician on clinical studies. We are looking for a Biostatistician with a Masters Degree in biostatistics, statistics or an other related scientific field and five years of relevant professional experience. A PhD in those fields are preferred. Qualified candidates must be familiar with clinical trial design and analysis activities and basic knowledge of regulatory guidelines. You must have expertise in manipulating and analyzing

Our client is currently seeking a Clinical Research Coordinator with 1-2 years of experience. Neurology experience is a plus, but not required. Also, our client offers an exceptional benefits package and is looking to interview candidates ASAP! 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

Aerotek is currently looking for a qualified candidate that will serve as a lead Biostatistician on clinical studies. We are looking for a Biostatistician with a Masters Degree in biostatistics, statistics or an other related scientific field and five years of relevant professional experience. A PhD in those fields are preferred. Qualified candidates must be familiar with clinical trial design and analysis activities and basic knowledge of regulatory guidelines. You must have expertise in manipulating and analyzing

-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

DUTIES: -Identifies, evaluates and selects study centers -Obtain, review for appropriateness and process regulatory and administrative documents from study sites -Maintain clinical files -Track progress and status of contractual agreements (non-disclosure agreements, clinical trial agreements, contracts with vendors) -Manages central IRB, where applicable -Process/track safety information (IND Safety Reports/SAE Reports) to ensure regulatory compliance and real-time reconciliation of the clinical trial and

A Pharmaceutical company has an immediate opening for a Jr-level Clinical Research Associate with a good attitude in North Chicago, Illinois. The Clinical Research Associate is responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines and study protocol. Job Duties Include: -Responsible for training sites on protocol related issues. -Home-Based Regional Travel 20%. -Assisting staff in planning study conduct. -Writing basic study protocols. -Designing

SUMMARY: - Assists in the management and implementation of study protocols - Coordinating development of study materials and plans - Support Clinical project Manager RESPONSIBILITIES: - Performs essential documentation collection, review, and maintenance - Study tracking - Liaises with internal and external partners *MUST HAVE A BACHELORS DEGREE *MUST HAVE RECENT INDUSRTY EXPERIENCE (leading Pharma/Biotech/CRO) 3-5 years Join Aerotek Scientific LLC(SM), one of the fastest growing providers of scientific and

Aerotek's client in Waltham is looking for a Senior Clinical Research Associate to join their team. Our client is a life sciences company focused on the discovery, development and commercialization of novel molecular diagnostics based on biomarkers to improve patient outcomes and contain healthcare costs. The Senior Clinical Research Associate participates in the planning, designing, and executing of high quality clinical studies. This person works with confidential patient and company data, and interfaces with

Our client in the Central valley is looking for a Clinical Research Coordinator to join their amazing team. Job Requirements: *Must have a current RN License *Prior experience as an RN in an inpatient or outpatient setting, and/or research experience. *Knowledge of medical terminology, basic anatomy, physiology, pharmacology, and lab procedures enabling assessment of patient eligibility. *Knowledge of clinical research study principles. *Conduction of research protocols. *Maximize research study income. *Follow

Our client, a prestigious CRO located in Midtown Manhattan is in need of a SR Clinical Project Manager. This is a permanent opportunity with a competitive salary and comprehensive benefits. The responsibilities of the Project Manager will include: -Project management of multiple clinical trials -Act as primary liaison between the sponsor and CRO -In-house and on-site monitoring of trials as necessary (limited travel to NJ) -Managing study budgets and contracts -Reviewing and developing protocols -Reviewing

Aerotek Scientific is currently looking for a Clinical Research Coordinator to work for our client located in Phoenix. This is a large company with plenty of opportunity to grow. Qualified Candidates must have the following: -A minimum of 3 years experience as a Clinical Research Coordinator -Some experience in surgical clinical research. -Must be flexible with hours -Must be able to multi-task For immediate consideration please contact Erica Holder at (623) 518-1360 or by email at eholder@aerotek.com Join Aerotek