Covance Jobshttp://jobsearch.covance.com Dallas, TX jobs with Covance(c) 2009, Covance10Sat, 23 Jul 2016 10:55:22 EST1339813Associate Start Up Manager Early ClinicalAssociate Start Up Manager for Early Clinical Development Remote based position, openings nationwide Typically under the direction of the Project Manager/Sr. Project Manager/Project Director, the Associate Project Manager, Study Start Up oversees and manages the study start up phase of regional clinical trials. - Participate in the planning, management, and sharing of regional site start-up actihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339813Thu, 21 Jul 2016 13:16:11 GMT1339627Senior Manager Client Proposals Clinical Trial ServicesSenior Manager Client Proposals for Late Phase Clinical Trial Services Remote Home Based Working Option for highly Experience d candidates Working with a global team you will be a vibrant, self-motivated, process driven self-starter, possessing proven ability to deliver in a fast paced, high volume environment, working on both new and existing business opportunities. The primary remit of the rolhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339627Thu, 21 Jul 2016 05:59:14 GMT1339194Start Up Associate Project Manager ECDStart Up Associate Project Manager for Early Clinical Development Remote based position, openings nationwide Typically under the direction of the Project Manager/Sr. Project Manager/Project Director, the Associate Project Manager, Study Start Up oversees and manages the study start up phase of regional clinical trials. Responsibilities typically include contributing to the development and managehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339194Tue, 19 Jul 2016 12:39:03 GMT1339178Associate Start Up Manager Early ClinicalAssociate Start Up Manager for Early Clinical Development Remote based position, openings nationwide Typically under the direction of the Project Manager/Sr. Project Manager/Project Director, the Associate Project Manager, Study Start Up oversees and manages the study start up phase of regional clinical trials. - Participate in the planning, management, and sharing of regional site start-up actihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1339178Tue, 19 Jul 2016 12:38:05 GMT1338801Manager Investigator Health System RelationshipsThe Manager, Investigator & Health System Relationships is responsible for improving aspects of site identification and study performance by developing and maintaining highly effective relationships with our research partners. This includes understanding and driving innovations that are either envisioned from within Covance or are proposed by our research and channel partners. This role is responshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338801Mon, 18 Jul 2016 12:45:35 GMT1338732Project Mgr Regulatory AffairsGlobal Regulatory Affairs (GRA) is responsible for ensuring the quality of documents and submissions to regulatory authorities globally in support of both investigational and marketed product activities. GRA is also responsible for authoring medical & regulatory documents and providing strategic input for projects as required. The Project Manager, Regulatory Affairs is responsible for the managemhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338732Mon, 18 Jul 2016 12:45:24 GMT1338305Research Nurse IWe are currently hiring a Clinical Research Nurse for our Clinical Pharmacology site in Dallas, TX. MUST BE WILLING to work a flexible rotating shift or a straight night shift (a shift differential incentive will be provided). Strong technical skills (preferred) All levels of Experience . The Research Nurse will be responsible for study unit activities in the conduct of clinical trials with emphttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338305Thu, 14 Jul 2016 18:01:13 GMT1338182Sr QA Auditor I eTMF Audit Experience NeededSenior Auditor I Location: Virtual/Remote Travel: Up to 30% Covance is looking for a Senior Auditor to join the Regulatory team. This person will have Experience with TMF audit and auditing in a GCP environment. Responsibilities: - Conducts complex, directed, and/or time sensitive QA audits - Provides suitable recommendations for audit observations; ensures auditees deliver appropriate CAPAs anhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1338182Thu, 14 Jul 2016 14:16:27 GMT1336341Sr Associate CDS Clinical InformaticsThe Senior Associate, CDS - Clinical Informatics will: - Provide day to day support to a local Operational Strategy & Planning team so as to efficiently and effectively model and forecast from feasibility data and other relevant information to allow for the development of evidence-based planning associated with the implementation and conduct of clinical trials - Coaching and mentoring of relevanthttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1336341Thu, 07 Jul 2016 12:37:19 GMT1336190Account Director Market AccessCovance is recruiting an Account Director for its growing Market Access group. This position can be located in Gaithersburg, MD, San Diego, CA, Greenfield, IN or remotely. The Account Director is not a sales or marketing position. The Account Director is responsible for developing, maintaining, and expanding client relationships. This includes overseeing the strategic functions of the InTeleCentehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1336190Thu, 07 Jul 2016 05:22:08 GMT1335424Clinical Team LeadCovance is currently seeking a Clinical Team Lead (CTL) NATIONWIDE to function as the leader for the clinical team in our Clinical Operations Phase II-IV group. Up to 5K sign on bonus for Experience d, qualified CTL candidates The Clinical Team Lead (CTL) is the leader for the clinical team in our Clinical Operations Phase II-IV group. The Clinical Team Lead is a member of the Core Project Team http://jobsearch.covance.com/CustomJobDetail.aspx?id=1335424Wed, 06 Jul 2016 05:27:12 GMT1335015Clinical Research Associate I CRA Monitoring Excellence Academy MEA Research Coordinators and Nurses NeededClinical Research Associate I – Monitoring Excellence Academy Location: Remote/Home Based Are you an Experience d Research Nurse or Study Coordinator? Join the Covance Monitoring Excellence Academy (MEA) and train to be a CRA. If you bring the therapeutic expertise, we will train you to be a top notch CRA. You'll be hired into a full time CRA I position, the first 3-6 months of which will providehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1335015Tue, 05 Jul 2016 15:09:06 GMT1334783Sr CRA Line Manager Home BasedSr. CRA Line Manager Location: Remote/Home-based Covance's Early Clinical Development team is seeking a Sr. CRA Line Manager for a home-based opportunity. Responsibilities include: - Responsible for appropriate management and resolution of performance issues - Measure performance indicators for assigned staff within Clinical Operations - Identify individual training needs and assist in the conduhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334783Fri, 01 Jul 2016 14:51:45 GMT1334754Associate Manager Early Clinical Development Home BasedAssociate CRA Line Manager, Early Clinical Development Location: Remote/ Home-based Covance's Early Clinical Development (ECD) team is seeking an Associate CRA Line Manager for a home-based opportunity. In this role you'll work with our Monitoring Excellence Academy new-to-role CRAs and support their training in the CRA position. Managing a team of CRAs at Covance can lead you to a more fulfillihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334754Fri, 01 Jul 2016 14:49:33 GMT1334591Regulatory Specialist IDuties/Responsibilities: - Provide assistance to staff and clients regarding regulatory responsibilities, where appropriate. - Maintain accurate and complete regulatory documents for all clinical studies conducted in the division of clinical pharmacology. - Responsible for weekly filing of Study Master Files and document submission for Trial Master Files - Assist with regulatory training for http://jobsearch.covance.com/CustomJobDetail.aspx?id=1334591Fri, 01 Jul 2016 04:38:26 GMT1334374Clinical Research Associate I CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associate I (0-2 years monitoring Experience ) Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines ahttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334374Thu, 30 Jun 2016 13:40:30 GMT1334295Senior Clinical Research Associate CRA up to 15K Sign on Bonus Seeking Remote Senior Clinical Research Associates (4+ years monitoring Experience ) Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelihttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334295Thu, 30 Jun 2016 13:40:29 GMT1334216Clinical Research Associate II CRA up to 15K Sign on Bonus Seeking Remote Clinical Research Associates II (2-4 years monitoring Experience ) Nationwide (US and Canada) in all phases and in all therapeutic areas! Ability to travel 65-80% is a must! Up to 15K sign on bonus for Experience d CRAs!! The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelineshttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334216Thu, 30 Jun 2016 13:40:27 GMT1334197Clinical Research Associate CRA Limited Travel up to 15K sign on Remote/Home Based opportunities available near Dallas, TX and Evansville, IN and Daytona Beach, FL. These are limited travel roles! Covance is looking for Experience d Clinical Research Associate (CRA) to monitor at our Phase I clinical research units.. This is a field based role, but the bulk of sites you'd be visiting are at the unit or in the surrounding area. This is an ideal position for a Chttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334197Thu, 30 Jun 2016 13:40:23 GMT1334195Clinical Research Associate CRA Limited Travel up to 15K sign on Remote/Home Based opportunities available near Dallas, TX and Evansville, IN and Daytona Beach, FL. These are limited travel roles! Covance is looking for Experience d Clinical Research Associate (CRA) to monitor at our Phase I clinical research units.. This is a field based role, but the bulk of sites you'd be visiting are at the unit or in the surrounding area. This is an ideal position for a Chttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334195Thu, 30 Jun 2016 13:40:23 GMT1334196Clinical Research Associate CRA Limited Travel up to 15K sign on Remote/Home Based opportunities available near Dallas, TX and Evansville, IN and Daytona Beach, FL. These are limited travel roles! Covance is looking for Experience d Clinical Research Associate (CRA) to monitor at our Phase I clinical research units.. This is a field based role, but the bulk of sites you'd be visiting are at the unit or in the surrounding area. This is an ideal position for a Chttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334196Thu, 30 Jun 2016 13:40:23 GMT1334194Clinical Research Associate CRA Limited Travel up to 15K sign on Remote/Home Based opportunities available near Dallas, TX and Evansville, IN and Daytona Beach, FL. These are limited travel roles! Covance is looking for Experience d Clinical Research Associate (CRA) to monitor at our Phase I clinical research units.. This is a field based role, but the bulk of sites you'd be visiting are at the unit or in the surrounding area. This is an ideal position for a Chttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334194Thu, 30 Jun 2016 13:40:23 GMT1334141Senior Manager Monitoring Data Flow OptimizationThis role will focus on Covance's Xcellerate Monitoring Solution Development e.g. leading product development, process excellence, internal initiatives. The Senior Manager, Central Monitoring is a key member of the global Risk Based Monitoring Team and has overall responsibility and accountability for the execution and implementation of Risk Based Monitoring activities. The Senior Manager, Centrhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1334141Thu, 30 Jun 2016 13:39:25 GMT1333822Sr Manager Central MonitoringCovance needs a Senior Manager, Central Monitoring who: - Prepares and provides RBM proposal text & review of costing, contributes to proposal strategy and development. - Collaborates in the development of RBM sponsor presentations/bid defense support. - Oversees at a study or tactical level tracking data to ensure it is used to effectively to anticipate and mitigate risk. - Leads, plans, preparehttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1333822Wed, 29 Jun 2016 14:52:01 GMT1333804Screening Technician IResponsibilities/Duties: - Read protocols in order to assist with screening procedures necessary to determine participant qualification as well as to understand the Inclusion and Exclusion criteria for the study. - Work with Project/Study Manager and Screening/Recruitment Supervisor to arrange any special screening procedures that may be necessary for the study. - Provide assistance to ensure http://jobsearch.covance.com/CustomJobDetail.aspx?id=1333804Wed, 29 Jun 2016 14:51:57 GMT1325749Research Tech IICovance is recruiting for a Research Technician II in its Dallas, TX location. This is an exciting time to join our growing company! **Must be able to work a rotating shift Duties and Responsibilities include: - Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings - Preparation and accurate recording of ECGs/Holters - Collection and processing of biolohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325749Fri, 17 Jun 2016 12:31:31 GMT1325573Director Site Activation pre awardThe Project Director oversees and directs international clinical trials in the start up phase. Responsibilities typically include developing and managing budgets, timelines, and quality guidelines for projects, thereby ensuring that expectations are met while identifying and mitigating risks. They also drive documentation for the project, ensuring the accuracy and quality of regulatory data. They http://jobsearch.covance.com/CustomJobDetail.aspx?id=1325573Fri, 17 Jun 2016 05:29:53 GMT1325279Experienced Histotechnician Pathology 500 Sign On Bonus and Relocation Offered Research Assistant/Histotechnician - Pathology ***This position is based in Madison, WI. $500 Sign On Bonus and Relocation assistance is available. Covance is seeking a Research Assistant to join the Pathology team in Madison, WI. You should have prior histology and necropsy Experience and may be eligible for a sign on bonus.* Job Duties and Responsibilities: - Performs necropsy and/or histolohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1325279Thu, 16 Jun 2016 14:57:36 GMT1324548Associate Scientific DirectorThe Associate Scientific Director will support commercial, operational and biometrics teams for Global Clinical Pharmacology (GCP), providing input into study design, acting as GCP representative on molecule development teams and performing scientific review of biometrics deliverables. This position must be located at one of our facilities in: Dallas, TX, Evansville, IN or Madison, WI. Re-locatiohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324548Tue, 14 Jun 2016 15:12:59 GMT1324545Associate Scientific DirectorThe Associate Scientific Director will support commercial, operational and biometrics teams for Global Clinical Pharmacology (GCP), providing input into study design, acting as GCP representative on molecule development teams and performing scientific review of biometrics deliverables. This position must be located at one of our facilities in: Dallas, TX, Evansville, IN or Madison, WI. Re-locatiohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324545Tue, 14 Jun 2016 15:12:59 GMT1324543Associate Scientific DirectorThe Associate Scientific Director will support commercial, operational and biometrics teams for Global Clinical Pharmacology (GCP), providing input into study design, acting as GCP representative on molecule development teams and performing scientific review of biometrics deliverables. This position must be located at one of our facilities in: Dallas, TX, Evansville, IN or Madison, WI. Re-locatiohttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1324543Tue, 14 Jun 2016 15:12:59 GMT1320537Senior Medical Writer ICovance is seeking a Senior Medical Writer to join our Global Medical Writing team. The Senior Medical Writer must have Experience in clinical trials documentation. The Sr. Medical Writer is a remote position. The Global Medical Writing department is responsible for ensuring that work undertaken meets the requirements of government regulatory agencies locally and worldwide. This responsibility http://jobsearch.covance.com/CustomJobDetail.aspx?id=1320537Thu, 26 May 2016 15:12:18 GMT1312266Senior Site Management AssociateCovance is hiring a Senior Site Management Associate to be remotely based within the US. Responsibilities / Duties: *Provide training and direction to the study team regarding adherence to Covance Standard Operating Procedures (SOPs), Project-specific Controlled Documents, FDA and ICH Guidelines, GPPs, and GCPs *Oversee the development and maintenance of tracking systems for projects *Conduct http://jobsearch.covance.com/CustomJobDetail.aspx?id=1312266Wed, 04 May 2016 14:39:29 GMT1280108Project DirectorCOVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We are currently recruiting for a Project Director that will lead a core project team and facilitate team's ability to lead extended/complete relevant studies. This role is a permanent, full-time position that can be either office or home based in a European couhttp://jobsearch.covance.com/CustomJobDetail.aspx?id=1280108Mon, 08 Feb 2016 15:17:56 GMT