وظائف بحث سريري في International

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...

GROUP OVERVIEWGovernment Affairs drives our business by shaping the policy and regulatory environment to accelerate digital payments ensuring Visa is the best way to pay and be paid for everyone everywhere. We excel with clients governments and partners to enable everyone to participate fully in the...

You will lead the identification pursuit and execution of government-funded programs on behalf of the firm and its clients. This role is responsible for the full lifecycle of government contracts and grants - from capture and proposal leadership through successful delivery of high-impact healthcare...

Role Summary The Senior Manager People & Purpose is responsible for overseeing all functions in the People and Purpose Department. Key responsibilities include but are not limited to; maintaining and enhancing the firms human resources by planning implementing and evaluating employee relations and h...

Date Posted:Country:United States of AmericaLocation:Sarasota Cattlemen OfficeWHY JOIN FCS At Florida Cancer Specialists & Research Institute we believe our people are our strength and we invest in addition to having a positive impact on the people and communities we serve associates benefit from s...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...

JOB DESCRIPTION:Job DescriptionPrimary Job Function:The Site-ICRA I based in India is primarily responsible for support services in partnership and collaboration with the US and EMEA Clinical Site Operations team. Primary focus is on providing and leading support of site management activities such...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

Fortrea is growing his FSO department! We are actively looking for a CRA I to join our team.Responsibilities:Responsible for all aspects of site management as prescribed in the project plans.General On-Site Monitoring Responsibilities.Ensure the study staff who will conduct the protocol have receive...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials ac...

Current Employees:If you are a current Staff Faculty or Temporary employee at the University of Miami please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position please review this tip sheet.The University of Miami/UHealth Dep...

Job Overview:Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. Assures the implementation of project plans as assigned.Summary of Responsibilities:Responsible for all aspects of study s...