better Biotech Pharma Job in North Carolina

A Worldwide Clinical Research Organization (CRO) is searching for a Clinical Data Manager I in their Durham, NC location. Provided below are the necessary responsibilities and qualifications for this position. Roles/Responsibilities: The role of the Clinical Data Manager (CDM) is to independently perform all clinical data cleaning activities on assigned projects, commensurate with experience and/or project role. Key activities include data validation, generation and integration of queries, coding of clinical

We are actively recruiting for a top-notch Senior Clinical Project Manager/Director, with strong bkgd in critical care trials, for key role in highly-regarded niche CRO. This company has earned a growing reputation for excellence, efficiency and employee-friendly policy. Its client base is expanding as is its therapeutic breadth. Seek a top-notch clinical project management leader to drive challenging and important global Critical Care trials. Critical care bkgd is essential. Experience with transplant

Clincial Staff Pharmacist Job Location: Wilmington, NC Category: Pharmacy - Staff Pharmacist Apply Now! Back to Results Experienced clinical staff pharmacist needed for a small community hospital in South Carolina. This 40 bed facility is looking for a pharmacist with prior hospital and clinical rotations to work Monday - Friday and every other weekend. Please call Lara Parker at 866-77-0734 or email me at lara.parker@soliant.com.

Medical Director Clinical Development Tracking Code 2009855 Job Description Based in Durham, NC and reporting to the Vice President of Regulatory and Clinical Affairs,the Medical Director of Clinical Development isresponsible for leading Smith & Nephew's, global clinical study strategy for the Biologics & Spine business unit. The role will work closely with Regulatory Affairs, Research and Development, Clinical Therapies, Business Development and Commercialization/Marketing team. The Medical Director is responsible

Must have no less than 3 total years in discrepancy management and be able to verbalize detailed processes of their experience. Must be able to detail the following: 1. Resolving discrepancies to zero count and if not zero, what was the rationale behind all discrepancies not being resolved 2. Tracking down missing pages and provide detail. Job Requirements: - 5 years experience minimum - Must have had to lock/close a study at study end - Global Phase III study management/ownership - Must have Oracle

3 contractors for data cleaning. Here are high level bullet points for requirements: - 5 years experience minimum - lock/close a study at study end - Global Phase III study management/ownership - Must have no less than 3 total years in discrepancy management and be able to verbalize detailed processes of their experience. Must be able to detail the following: 1. Resolving discrepancies to zero count and if not zero, what was the rationale behind all discrepancies not being resolved 2. Tracking down missing

Ockham is a global provider of resources to the Biotechnology and Pharmaceutical Industry. We work with companies involved with clinical trials and other market approval processes to help them deliver their products on time and on budget.One of our clients in Raleigh, NC has an immediate need for a Biostatistician. This is a permanent position. Biostatistician is responsible for the statistical deliverables and/or exploratory analysis of important clinical development consequence for one or more clinical

PharmaNet Resource Solutions is the new global alternative for flexible staffing with experienced clinical development professionals. We currently have an exciting opportunity for a Contract Clinical Data Analyst in Cary, NC. - Perform data review and query generation - Define edit checks to be programmed for the study/project - Review programmed edit checks - Track study progress and issue periodic status reports - Update the database to correct errors - Code

Clinical Data Analyst Permanent position available in the RTP area for a Clinical Data Analyst! Qualified candidates will have a strong background in reports programming and data integration task. They also must be highly proficient in SQL, PL/SQL and reporting tools for Oracle and SQL Server databases. Experience integrating data into relational databases, familiarity CDISC Lab is a PLUS, other healthcare/research standards are a plus. Salary range of $58,000 to $68,000 annually. Job Requirements

INC Research is headquartered in Raleigh North Carolina with 25 offices and a presence in 32 locations worldwide...

Department Biostatistics Clinical Programming Location USA North Carolina Durham Employment Type Full Time Job...

Senior Clinical Project Manager Job ID: 1386 Location: US-NC-Morrisville Category: Research and Development - Clinical More information about this job: Overview: The Senior Clinical Project Manager (Sr. CPM) is responsible for assuming a leadership role to ensure the operational milestones and timelines of clinical studies are achieved. Other responsibilities include advising Clinical Project Managers in the leading of vendor meetings, overseeing the design and development of CRFs, Informed Consents, specific

Prefer seasoned Clinical Data Manager/coordinators with 5 -7 years experience minimum Prefer candidates who have had to lock/close a study at study end Global Phase III study management/ownership Must have no less than 3 total years in discrepancy management and be able to verbalize detailed processes of their experience. Must be able to detail the following: 1. Resolving discrepancies to zero count and if not zero, what was the rationale behind all discrepancies not being resolved 2. Tracking down missing

Clinical Data Analyst Permanent position available in the RTP area for a Clinical Data Analyst! Qualified candidates will have a strong background in reports programming and data integration task. They also must be highly proficient in SQL, PL/SQL and reporting tools for Oracle and SQL Server databases. Experience integrating data into relational databases, familiarity CDISC Lab is a PLUS, other healthcare/research standards are a plus. Salary range of $58,000 to $68,000 annually Requirements Analyzes

PRA International is one of the world's leading global clinical research organizations, conducting clinical trials in 65 countries across six continents. PRA provides outsourced clinical services across all phases of pharmaceutical and biotech drug development. Through its 30+ years of experience, PRA has developed the operational and therapeutic expertise to provide high quality, global service while maintaining our differentiating PERSONAL ELEMENT of commitment to excellence. We currently have openings

PRA International is one of the world's leading global clinical research organizations, conducting clinical trials in 65 countries across six continents. PRA provides outsourced clinical services across all phases of pharmaceutical and biotech drug development. Through its 30+ years of experience, PRA has developed the operational and therapeutic expertise to provide high quality, global service while maintaining our differentiating PERSONAL ELEMENT of commitment to excellence. We currently have openings

Department Biostatistics Clinical Programming Location USA North Carolina Durham Employment Type Full Time Job...

ClinForce is currently seeking a Senior Clinical Research Associate - CRA for Durham, NC. Successful candidate will manage study process to ensure adherence to protocol, SOPs, GCP/ICH Guidelines, applicable regulatory requirements and other documentation requirements. Candidate will monitor vendors and other service providers for quality of service as well as initiate and maintain expedited identification, retrieval and review of study documents particularly those required for site activation/study start-up

ClinForce is currently seeking a Senior Clinical Research Associate - CRA for Durham, NC. Successful candidate will manage study process to ensure adherence to protocol, SOPs, GCP/ICH Guidelines, applicable regulatory requirements and other documentation requirements. Candidate will monitor vendors and other service providers for quality of service as well as initiate and maintain expedited identification, retrieval and review of study documents particularly those required for site activation/study start-up

excellent organizational skills and a current North Carolina driver s license...

language and will have a current North Carolina driver s license...

Clinical Pharmacist needed in North Carolina near the Outer Banks...My client North Carolina s premier healthcare provider who serves...Pharmacy or PharmD Licensure North Carolina Board of Pharmacy Certification Certifications in...

language and will have a current North Carolina driver s license...

excellent organizational skills and a current North Carolina driver s license...

The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking a Sr. Director, Biostatistics to head our Biostatistics department in RTP, NC.

A Worldwide Clinical Research Organization (CRO) is searching for a Clinical Data Analyst in their Durham, NC location. Provided below are the necessary responsibilities and qualifications for this position. Roles/Responsibilities: The role of the Clinical Data Analyst (CDA) is to independently perform all clinical data cleaning activities on assigned projects, commensurate with experience and/or project role. Key activities include data validation, generation and integration of queries, coding of clinical data

A Worldwide Clinical Research Organizaion (CRO) is searching for an experienced Clinical Drug Safety Specialist located in their Raleigh/Durham, RTP, NC office location. Job duties and responsibilities will include but are not limited to the below criteria. Job Description: The function of the Drug Safety Specialist includes overseeing the case handling and processing of clinical trial and spontaneous postmarketing events, assisting in the management and analysis of safety data with a particular emphasis on

- - - Project Manager Research Triangle Park, NC Cenduit, LLC, a joint-venture between Quintiles and ThermoFisher, is looking for a Project Manager for our location in Research Triangle Park, NC. This is a rare opportunity to join a new organization in the early stages and be part of our exciting future! Cenduit was founded in May 2007 and emerges from a robust tradition of clinical development and clinical supply chain expertise from two world leaders. Cenduit provides clients with state-of-the-art

and current licensure to practice in North Carolina BS degree from recognized college or...

A Clinical Research Organization is searching for an immediate Drug Safety Specialist out of their office located in Raleigh-Durham, NC. A nursing or pharmacist background is preferred but not required for this opportunity. Please find details below for this contract opportunity. Description: Serve as Pharmacovigilance (PhV) team member and project team lead, with supervision. Assist PhV management in building a productive team environment among assigned staff and between other sections and departments. Obtain

Senior/ Principle Clinical Research Associate Job ID #:4059 Location:NC - RTP Functional Area:Research and Development Department:MED6873000 - Medical Affairs Position Type:Full - Time Regular Education Required:Associates Degree Experience Required:5 - 7 Years Relocation Provided:

Biostatistician Location: Durham, NC Category: Engineering Status: Direct Hire Reference: US_EN_2_108165_131507 Salary: N/A Posted: September 04,2009 Adecco Technical is currently seeking a lead biostatistician for a full time permanent opportunity in Durham, NC with a large, growing medical device/biotechnology company. The description and requirements are listed below. Relocation package is availabe, along with competitive salary structure and benefits. Position Description Understand and manage the

CLINICAL DATA ANALYST COMPANY INFO: MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device industries. We specialize in the nationwide recruitment of clinical trials personnel. Our client is a proven and committed partner to drug developers and medical device manufacturers looking to bring innovative new products to market and is seeking to add a Clinical Data Analyst to their team in Durham, NC or Lowell, MA. RESPONSIBILITIES

our Research Triangle Park office in North Carolina and the position requires 70 80...

Clinical Pharmacists specializing in Pediatric Medicine and or Critical Care Established Financially Stable 700 bed hospital in North Carolina...Required Qualifications Licensed as a Registered Pharmacist in the State of North Carolina or transfer eligible...

Member of clinical research team responsible for data management activities across multiple trials. Activities include assisting in data entry, query processing, site management, data reporting and other data management activities in support of clinical trial projects. ESSENTIAL FUNCTIONS: Perform data management activities on both paper based and Electronic data capture (EDC) studies. Major activities include: CRF data review, preparation for entry, query processing, discrepancy management

Our client, a RTP-based specialty pharmaceutical firm, is experiencing significant growth and is looking to bring on a very sharp and knowledgeable Safety professional for key role within its Safety function. Role will require experience with post-marketed products. Seek a high caliber candidate who enjoys a growing dynamic setting. Responsibilities will include all tasks related to the collection, processing, reporting and analysis of adverse events for marketed products. The successful candidate will ensure

Our client, a RTP-based pharmaceutical company that is undergoing tremendous growth, is actively recruiting for a top-tier Clinical Research professional, with bkgd as a monitor, for key role on its Clinical Operations team. Company has several marketed products and many more in the pipeline. It outsources significant clinical duties to "best of class" CROs. The Senior Clinical Project Manager will manage all day-to-day clinical trials activities for assigned drugs. There is a lot to do. Seek a top-notch

Clinical Data Analyst Permanent position available in the RTP area for a Clinical Data Analyst! Qualified candidates will have a strong background in reports programming and data integration task. They also must be highly proficient in SQL, PL/SQL and reporting tools for Oracle and SQL Server databases. Experience integrating data into relational databases, familiarity CDISC Lab is a PLUS, other healthcare/research standards are a plus. Salary range of $58,000 to $68,000 annually. Job Requirements

This is a full time position that is office based in Chapel Hill North Carolina...

INC Research is headquartered in Raleigh North Carolina and has a presence in 40 locations worldwide...

A Worldwide Pharmaceutical Company is searching for an experienced Clinical Drug Safety Specialist located in their Raleigh/Durham, RTP, NC office location. Job duties and responsibilities will include but are not limited to the below criteria. Job Description: The function of the Drug Safety Specialist includes overseeing the case handling and processing of clinical trial and spontaneous postmarketing events, assisting in the management and analysis of safety data with a particular emphasis on support to clinical

Back to Results Permanent Clinical Pharmacist Job on the beautiful coast in North Carolina...

Pharmacy or PharmD Licensure North Carolina Board of Pharmacy Certification Certifications in...

An innovation driven Pharmaceutical Corporation in North Carolina has a need for a Sr...

Experienced Clinical Research Coodinator- Alzheimer's Memory Center Conduct study for clinical trails at the investigator site. Consult patients for study eligibility according to protocol and criteria. Perform ECG. Neurology expirience prefered, but not necessary. Job Requirements: Qualifications. Bachelor degree required. Ability and authorized to draw blood. Ability to perform ECG requeired.

Clinical Data Analyst / Programmer (Electronic Data Control) Permanent position available in the RTP area!! Perm salary range of $70,000 to $82,000 EDC Database Development Responsibilities: Develops, tests, and maintains eCRF screens per client requirements and specifications Develops, tests and maintains data validation code, triggers, and alerts per client specifications Develops complex rules and user defined functions for data validation. Job Requirements:

Our client, an emerging biotech with several cardiovascular compounds in clinical trials, has an immediate need for a very sharp, capable and versatile Project Manager for key role on its R&D team. The company is developing (amongst others) two compounds that are highly anticipated in the cardiovascular market. Industry leaders are involved as advisors and investors. Seek a top-notch PM with the skills, knowledge and enthusiasm to drive the clinical trials efforts. The focus of the role will be to independently

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

This position will perform management functions relating to the administrative and scientific activities of specific project work and team members: - Oversee statistical aspects in the design and analysis of clinical trials, including project management, statistical analysis, report preparation, and advising other project statisticians - Function as Biostatistics Project Leader for multiple protocols, projects, or NDA projects, including coordinating with other PPD divisions and interacting with the client