Covance Jobs - Page 5 | CareerArc

Jobs at Covance - Page 5

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Senior In-House CRA

Covance by Labcorp - Chicago, IL

Job Overview: Whether it's at home, school, the office or other alternate location, GlobalCare's ambulant care services for clinical trials conveniently bring visits to the study patient. GlobalCare maintains a global network of multi-lingual Country Coordinators and local traveling service providers (nurses and physicians). We are seeking a Senior In-house CRA to jo...

Senior Clinical Data Coordinator

Covance by Labcorp - BC, Canada

Job Overview: The Clinical Data Management team is seeking candidates for a Senior Clinical Data Coordinator role. The Senior Clinical Data Coordinator will be remotely located anywhere within the United States or Canada. Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation activit...

Senior Clinical Data Coordinator

Covance by Labcorp - Montreal, QC, Canada

Job Overview: The Clinical Data Management team is seeking candidates for a Senior Clinical Data Coordinator role. The Senior Clinical Data Coordinator will be remotely located anywhere within the United States or Canada. Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation activit...

Budget Project Associate

Covance by Labcorp - Madison, WI

Job Overview: Covance is now part of LabCorp. We are a leading global life sciences company that is deeply integrated in guiding patient care, providing comprehensive clinical laboratory and end-to-end drug development services. With a mission to improve health and improve lives, LabCorp delivers world-class diagnostic solutions, brings innovative medicines to patients faster and uses techno...

Senior Clinical Data Coordinator

Covance by Labcorp - Durham, NC

Job Overview: The Clinical Data Management team is seeking candidates for a Senior Clinical Data Coordinator role. The Senior Clinical Data Coordinator will be remotely located anywhere within the United States or Canada. Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation activit...

Senior Clinical Data Coordinator

Covance by Labcorp - Raleigh, NC

Job Overview: The Clinical Data Management team is seeking candidates for a Senior Clinical Data Coordinator role. The Senior Clinical Data Coordinator will be remotely located anywhere within the United States or Canada. Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation activit...

Budget Project Associate

Covance by Labcorp - Princeton, NJ

Job Overview: Covance is now part of LabCorp. We are a leading global life sciences company that is deeply integrated in guiding patient care, providing comprehensive clinical laboratory and end-to-end drug development services. With a mission to improve health and improve lives, LabCorp delivers world-class diagnostic solutions, brings innovative medicines to patients faster and uses techno...

Biostatistician 2

Covance by Labcorp - Greece

Job Overview: Biostatistician 2 required to work for Covance by Labcorp supporting the Lead Biostatistician on studies in Phases I to IV You will be employed by Covance and work within our FSPx department 100% dedicated to one Sponsor The Sponsor is a top 20 pharmaceutical company Office based or home based in Netherlands Candidates mus...

Start-Up Specialist

Covance by Labcorp - Osaka, Osaka, Japan

Job Overview: トップグローバルCROであるCovanceの新薬開発の国際共同治験において、各施設との契約締結までのプロセスを一括管理していただくStart Up Specialistを募集しています。 こちらのポジションで行って頂く業務は、主に上記に関わるプロセスの管理と必須文書の確認・承認を実施していただきます。 具体的には、下記の通りとなっています。 【プロセスの管理】 ・施設立ち上げ時の同意説明文書の作成補助・契約締結・費用の合意に向けたCRAの内勤業務 ・個々の施設における治験文書および契約書の準備状況について、関係者に情報提供 ・治験契約書の作成補助 ・治験の各種マイルストーンに関連したデータをデータベースに入力・管理 ・必須文書のQC点検の実施...

Laboratory Technician I

Covance by Labcorp - England, United Kingdom

Job Overview: About Covance by Labcorp Your new employer is Covance by Labcorp, the world's most comprehensive drug development company, dedicated to improving health and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along ...

Assoc Dir Reg Sub

Covance by Labcorp - Tokyo, Tokyo, Japan

Job Overview: IVD及びCDxを開発するクライアントに対して、製品開発に関わる薬事規制や承認申請等に向けての助言を行うとともに、承認申請に関わる資料を作成する。 PMDAとの対面助言( IVD、CDx及び医薬品)における相談資料のうちCMC/ QAに関わる事項について、Regulatory Strategy部門と協力してその作成や案のレビューを行う。 承認申請、先駆的医薬品やオーファンの指定申請等のCMC/ QAに関わる薬事関連業務を行う。 ビジネス・ディベロップメントチームから要請があれば、CMC/ QAの経験・知識をもとにクライアントにプレゼンを行う。 Education/Qualifications: 海外クライアントとのテレカンが可能なビジネスレベルの英語力 Exp...

Senior Medical Writer

Covance by Labcorp - Durham, NC

Job Overview: Senior Medical Writer Remote in the United States Full-Time Medical Writers in the Early Phase group would typically work on clinical documents for studies in the early phases of clinical development; this includes Phase I through IIa studies focused on safety, pharmacokinetics and pharmacodynamics. Responsible for preparation and coordination of clinica...

Start-Up Specialist

Covance by Labcorp - Tokyo, Tokyo, Japan

Job Overview: トップグローバルCROであるCovanceの新薬開発の国際共同治験において、各施設との契約締結までのプロセスを一括管理していただくStart Up Specialistを募集しています。 こちらのポジションで行って頂く業務は、主に上記に関わるプロセスの管理と必須文書の確認・承認を実施していただきます。 具体的には、下記の通りとなっています。 【プロセスの管理】 ・施設立ち上げ時の同意説明文書の作成補助・契約締結・費用の合意に向けたCRAの内勤業務 ・個々の施設における治験文書および契約書の準備状況について、関係者に情報提供 ・治験契約書の作成補助 ・治験の各種マイルストーンに関連したデータをデータベースに入力・管理 ・必須文書のQC点検の実施...

Manager - Regulatory CPC

Covance by Labcorp - United Kingdom

Job Overview: Are you currently working as a manager / leader within either industry, a CRO or a Consultancy and looking to develop you career by taking that next management role step? Do you want to make a difference working for a world leader in Crop Protection and Chemicals Development? ...

Sr. Safety Science Specialist

Covance by Labcorp - Bengaluru, KA, India

Job Overview: - Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial. This includes, but is not limited to: - Entry of safety data onto adverse event database(s) and tracking systems - Rreview of adverse events for completeness, accuracy and appropriateness for expedited reporting