وظائف بحث سريري في International

Location: Belgium - Hybrid Type: Full-timeDo you want to protect the safety & well-being of subjects and guarantee data quality Do you get energy from daily communication with investigators study coordinators and study teams Do GCP ICH E6 R2 and ISO 14155 have no secrets anymore for you Do you like...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (F...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (F...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (F...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies across development and manufacturing. Our expertise includes full-service capabilities resourcing and Functional Service (FSP) solutions.Th...

Location: Hybrid Type: Full-timeDo you get energy from coordinating dynamic clinical trials with a quality-driven and pragmatic approach Do you like to partner with many stakeholders Do GCP ICH E6 R3 and ISO 14155 have no secrets anymore for you You might be the Clinical Project Manager we are look...

Qarads IVD CRO is a clinical research organization (CRO) specializing in In Vitro Diagnostics (IVD) providing full-service solutions to support diagnostic development from concept to commercialization. With a growing portfolio of projects we are dedicated to delivering high-quality outcomes through...

Consultant Regulatory Affairs & Publishing Location: Hybrid (Spain or UK) Type: Full-timeThe QbD Group supports life sciences companies worldwide from idea to patient. QbDs team offersknowledge&tailored (software) solutionsin development clinical regulatory & compliance production and distribution...

Location: Hybrid Type: Full-timeWe are seeking a dynamic and experienced Expert in Clinical Performance Studies to join our team specializing in In Vitro Diagnostics (IVD). In this role you will be designing executing and overseeing clinical performance studies for in vitro diagnostic (IVD) product...

3 Months Contract with Local AuthoritySummaryThe Resident Liaison Officer (RLO) will be integral to supporting Enfield Councils energy-efficiency and retrofit programs facilitating major works across council homes. The role ensures residents are informed supported and engaged throughout these projec...

Responsibilities:Provides project management on large scale complex high profile and high risk projects for OPS I&IT initiatives. Ensures project deliverables meet clients business requirements on time scope and budget with a foc Senior Project Manager to:Collaborate with ITOD various levels for pro...

The role will be reporting into Clinical Operations Manager.Advance AbbVies pipeline by striving for excellence in clinical research turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. Partners with the investigator and site...

RThis is a remote role based in the US. Candidates must be physically located within the US.Have you ever wondered whether Millennials are truly different from Gen Z Or how emerging technologies will reshape our everyday lives At the NIQ Consumer Behavior and Insights team we help shape the products...

We are looking for a pharmacovigilance medical writer to join our team. The  Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to determine scheduling...

Triages incoming SAE information in order to fulfill timely reporting according to the authority/regulatory requirements.Participate in safety surveillance activities for assigned products; and also in area projects/goals. Identify and escalate problems to manager.Collecting analyzing and triaging A...

Start your career in clinical research streamlining communication maintaining systems and managing documents & information.Office-based - BelgradeThe scope of responsibilities will include:Maintenance of databases and tracking systemsWork with large amount of documents including their compiling proc...

We are seeking an experienced GCP GLP and GVP Quality Assurance Program Manager who will serves as a hands-on embedded Quality Assurance resource supporting clinical research nonclinical and pharmacovigilance activities for early- to late-stage pharmaceutical development focused on fluorescence imag...

PSI CRO is looking for an experienced project finance professional in the Clinical Research industry who will be responsible for creating managing negotiating and analyzing clinical project budgets as well as providing support with bids and contract management activities within the company.Responsib...

Dalhousie University and Nova Scotia Health (NSH) are seeking a qualified full-time ophthalmologist with subspecialty training in glaucoma to practice in a challenging and rewarding academic medical environment. The successful candidate will be granted a continuing appointment with the Faculty of Me...

The Chairholder will be provided protected time for research activities in accordance with departmental and program priorities. Appointment will include medical staff appointment by Nova Scotia Health. The appointment will include a continuing academic appointment in the Faculty of Medicine.The Chai...