Clinical Trials Jobs in Brooklyn

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

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...

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...

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...

Assists in the preparation and submission of clinical trial documents for review of ethics committees. Conducts identification, evaluation, qualification, initiation, monitoring and visits of investigators and sites (including close-out visits). Checks implementation of company st More...

Clinical Project/Trial Management of phase I-III clinical trials according to ICH-GCP guidelines Selection, Management and Coordination of Clinical Research Organization (CRO) and External Service Providers. Submissions to ethics committees and competent authorities Budget planni More...

Bachelor’s degree in life/health sciences or related discipline, or equivalent required. 6 to 8 years of relevant clinical research experience in a Clinical Research Organization/Pharmaceutical Company, with a minimum of 3 years of Project Management experience in a CRO or ph More...

Bachelor’s degree in life/health sciences or related discipline, or equivalent required. 6 to 8 years of relevant clinical research experience in a Clinical Research Organization/Pharmaceutical Company, with a minimum of 3 years of Project Management experience in a CRO or ph More...

Bachelor’s degree in life/health sciences or related discipline, or equivalent required. 6 to 8 years of relevant clinical research experience in a Clinical Research Organization/Pharmaceutical Company, with a minimum of 3 years of Project Management experience in a CRO or ph More...

Position: Clinical Data ManagerRequirement: Immediate JoinerLocation: HyderabadExperience: 3 to 10 Years Key Roles & Responsibilities: Provide leadership and vision to the team.Manage and deliver largescale highcomplexity studies across a range of sponsors and therapeutic areas.Ma 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...

Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company Solid experience with complex o More...

Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company Solid experience with complex o More...

Location: IC: CSR Street: 6701 Rockledge Drive Bldg: x Room: 3030 City: Bethesda State & Zip: MD 20892 Weekly Hours FT: 3040 hours per week Overall Position Summary and Objectives Provide support services to satisfy the overall operational objectives of the Center for Sc More...

Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company Solid experience with complex o More...

Job Title: Principal BiostatisticianLocation: HyderabadJob Type: FullTime Key Responsibilities:1. Biostatistical Analysis and Strategy: Develop statistical analysis plans for clinical trials. Collaborate with clinical teams to design studies and determine primary endpoints.2. St 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...

Support and provide scientific nonbiased information and data relevant to Therapeutic Area, and Pharmaceutical Products to external stakeholders (KOLs, Academic Institutions, Regulatory Authorities, etc..) to ensure safe effective utilization of Products, to advance the scientific p More...

Our Client a top Global Pharmaceutical Research Company is looking to utilize AI to streamline additional processes and expand capabilities in their Clinical Trials. The Clinical IT Project Manager should have previous exposure to: patient recruiting trial design data collection and p More...