Clinical Trial Psych Rater
il y a 1 semaine
Job Description :The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is evaluated, and live interaction with raters is conducted to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. Other Clinical Specialist responsibilities may include, but are not limited to, functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications.Required Experience, Knowledge, Skills:• Minimum of a master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing or Social Work, or equivalent.MD, DO or PhD preferred• Minimum of 3 years’ experience administering psychiatric assessments, ratings scales and/or structured clinical interviews.Specifically,Primary: YGTSS-R, TS-CGI-S, TS-CGI-C• Minimum of 3 years clinical experience with related psychiatric populations.• Minimum of 3 years' experience with administering scales in clinical research trials (not including graduate/doctoral research work).• Experience in central nervous system (CNS) trials preferred.• Strong interpersonal skills with ability to interact with all levels of personnel and clientele in a professional manner.• Excellent organization, attention to detail, time management and problem-solving skills.• Computer proficiency with Windows and Microsoft Office system and applications.Tasks/Responsibilities:• Participate in all orientation, training and calibration activities as required.• Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available).• Complete rater interactions and assigned tasks as scheduled.• Responsible for timely submission of all documentation associated with assigned tasks.*Current openings require fluency in English and a native speaker in the language needed for the trial.#LI-DNP #LI-Remote #LI-HCPNIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
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Senior Clinical Trial Manager
il y a 1 semaine
Zaventem, Belgique ICON Temps pleinICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...
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Clinical Research Lead
il y a 1 semaine
Zaventem, Belgique ICON Temps pleinWe are hiring a Clinical Research Lead, sponsor dedicated in Brussels, Belgium.Our client is a medicine company turning science into healing to make life better for people around the world. Would you like to become part of this team and take your next challenge with ICON Strategic Solutions?Apply today and we'll be happy to discuss this opportunity with...
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Intern - Clinical Research Associate, Multi-sponsor, Belgium
il y a 1 semaine
Zaventem, Belgique IQVIA Temps pleinThe IQVIA Internship provides you with the opportunity to gain relevant, project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future. You will be working in our **Clinical Trials Team** together with some of the most...
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Clinical Project Manager, FSP Belgium
il y a 1 semaine
Zaventem, Belgique IQVIA Temps pleinJob OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...
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Clinical Data Management Lead
il y a 1 semaine
Zaventem, Belgique IQVIA Temps pleinRESPONSIBILITIES Serve as primary point of contact for customer on data management deliverablesManage multiple large studies or program of studies (possibly global)Provide leadership and senior support to DTLs on multiple large global programs of global studiesProvide project management expertise working with customer data managers, key decision makers, and...
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Experienced Clinical Research Associate, FSP Belgium
il y a 1 semaine
Zaventem, Belgique IQVIA Temps pleinClinical Research AssociateIQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team CRA (Junior - Senior) . At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career...
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Zaventem, Belgique LivaNova PLC Temps pleinDescription of role, key tasks etcEnsure sponsor compliance to local and international government regulationsDrive Health Care Professionals (HCP) and Health Care Organizations (HCO) selection, activation, management and any close-out activities including all necessary documentationEstablish and maintain first-line contact with HCPs (mainly...
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Associate Medical Safety Director
il y a 1 semaine
Zaventem, Belgique IQVIA Temps pleinOur ever-growing Lifecycle Safety Medical team is expanding. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes, but is not limited to providing and maintaining of PV and risk management expertise to internal and external stakeholders, maintaining knowledge relevant to allocated product portfolios,...
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Contracts Associate
il y a 1 semaine
Zaventem, Belgique ICON Temps pleinAs a Contract Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You will prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a ClinicalResearch Organization responsible for contract negotiations. Provide support to the...
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Senior CRA
il y a 1 semaine
Zaventem, Belgique ICON Temps pleinJob Title: Clinical Research Associate (CRA)Location: BelgiumTravel Requirement: Up to 60%Summary:We are seeking a dedicated Clinical Research Associate (CRA) to join our team. In this role, you will be responsible for identifying, initiating, monitoring, and closing investigational sites for clinical studies. You will ensure that all activities align with...
