Clinical Trials Jobs in Senegal

Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drug More...

Job Title: Clinical Trials Manager Duration: 06 Months (Contract) Location: 333 Lakeside Drive Foster City CA 94404 Job Responsibilities: Serves as the key biomarker and bioanalytical operational (BBOps) contact with internal and external stakeholders for successful implementation More...

Roles & Responsibilities: Conduct audits of clinical trial study Conduct operations as per SOP Conduct vendor audits Maintain Quality system for clinical trial unit Maintain relevant documentation

Foster City CA Contract Duration: 636 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Clinical Trials Manager in the Foster City CA area. Hybrid Clinical Operations is responsible for the worldwide execution of all Phase I IV clinical trials across a More...

OverviewhVIVO are currently seeking an addition to our Data Entry team to work across our London sites in Whitechapel Canary Wharf East London.hVIVO conducts human challenge studies offering services to both pharmaceutical and biotechnology companies using a range of different clinica More...

Experience in data modelling using statistical methods to identify behavioural and data patterns. Industry experience would be advantageous but this is not clinical endpoint analysis so a different way of thinking about data and stats modelling is required.An interest and/or experienc More...

Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs More...

Job Title: Clinical Trial Coordinator Location: Santa Monica CA 90404 Duration: 12 months (contract) Shift Hours: Monday Friday Description: Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. Provides admin More...

This a Full Remote job, the offer is available from: Africa, EMEA Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTR More...

This a Full Remote job, the offer is available from: Africa, EMEA Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manag More...

Provide support to the Head of unit with many of the tasks involved with the smooth running of clinical trials in compliance with DDI processes. Collaborate in taking action to address issues as they arise Conceptualize and conduct short-term experiments and research activities in More...

Day to Day: This opportunity will be part of the clinical trials in a pharmacy. Bringing the trials to the people at their local pharmacy. The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruitin More...

Clinical Research CoordinatorAbout the jobRole DescriptionThis is a fulltime hybrid role for a Clinical Research Coordinator with Client. The Clinical Research Coordinator will be responsible for daytoday tasks related to clinical research including informed consent protocols research More...

Clinical Data Management Job DescriptionWe are looking for a detailoriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity ensuring the smooth and efficient flow More...

Responsibilities Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines and company SOPs. Assist in site qualification initiation and monitoring visits. Review and track clinical trial documentation ensurin More...

Location: IC: NIMH Street: 10 Center Drive Bldg: 10 Clinical Center Room: 4C438 City: Bethesda State & Zip: MD 20892 Weekly Hours PT: Less than 30 hours per week Total No. Of Hours 20 Overall Position Summary and Objectives The position will independently provide support s More...

Description: ** Locations: Foster City CA** Will Consider Remote for well qualified candidates ** **Candidates must be able and willing to work onsite ** Hybrid model accepted 2 to 3 days on site. The R&D Sourcing and Contracting Associate will be responsible for assistance in th More...

Duration : 12 months contract Locations: Foster City CA **Candidates must be able and willing to work onsite ** Hybrid model accepted 2 to 3 days on site. The R&D Sourcing and Contracting Associate will be responsible for assistance in the preclinical / research clinical sour More...

Undertake patient consultations and physical examinations, assessment and plan treatment requirements through clinics at a minimum of 4-5 time per week including evening clinic. Conduct CPET and provide consultation for patients through weekly clinics Liaise with other doctors, More...

Description: Manager Vendor Outsourcing ** Locations: Foster City CA** Will Consider Remote for well qualified candidates ** **Candidates must be able and willing to work onsite ** Hybrid model accepted 2 to 3 days on site. The R&D Sourcing and Contracting Associate will be resp More...