Job Posting Title Clinical Trial Psych Rater - Italian Speaking
41.000 € - 61.400 €IQVIA
Clinical Trial Psych Rater - Italian Speaking
Location: Remote/Virtual
Hours: Estimated 10–16 hours per month
Role: Clinical Specialist
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
Position Overview
The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation.
Key Responsibilities
Participate in all required orientation, training, and calibration activities.
Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.
Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.
Complete assigned tasks and rater interactions according to schedule.
Submit all required documentation accurately and on time.
Required Qualifications
Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
Experience:
Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically BEHAVE,-AD, E-BEHAVE-AD, BEHAVE-AD-FW, NPIC, ADAS-Cog; CGI-S, C-SSRS ).
Minimum 3 years of clinical experience with psychiatric populations.
Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).
Experience in CNS trials preferred.
Skills:
Strong interpersonal and communication skills for professional interaction at all levels.
Excellent organizational skills, attention to detail, time management, and problem-solving ability.
Proficiency with Windows and Microsoft Office applications.
Language Requirement
Current openings require fluency in English and native-level proficiency in Italian.
#LI-DNP #LI-Remote #LI-HCPN
IQVIA 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
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is €41,000.00 - €61,400.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
- ...Clinical Research Associate ICON plc is a world-leading healthcare... ...will design and analyse clinical trials, interpreting complex medical... ...will contribute to clinical trial monitoring activities, taking... ...after being certified as per Italian Law Prior experience in Oncology...Lingua italianaLavoro da remoto
- JOB DESCRIPTION Work Schedule Standard (Mon-Fri)... ...life-changing therapies. With clinical trials conducted in 100+ countries and... ...digital and decentralized clinical trial services. Your determination... ...Fluency in English and in Italian Valid Driver's License...Lingua italianaLavoro da remotoTempo pienoOrario flessibileDal lunedì al venerdì
- Job PurposeThe Clinical Trial Liaison Manager (CTLM) is responsible for site performance, trial delivery and Sponsor oversight across assigned countries... ....Required LanguagesFluent written and spoken English, Italian and another European languageTravel required in %...Lingua italianaRemoto
- ...the key scientific point of contact for clinical trial sites—supporting site engagement, education... ..., ideally in solid tumors.Fluent in Italian and English; additional fluency in Greek... ...based on a number of factors including job-related qualifications such as knowledge...Lingua italianaPart-timeTempo pienoDisponibilità immediata
- ...Start Up Associate IIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new... ...Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and contribute...ConsigliatoTempo pieno
- ...privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for... ...to groundbreaking advancements in the pharmaceutical industry.Job DescriptionClincial Data Manager plays a critical role in the...
- ...II ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment... ...Associate II at ICON, you will lead the initiation of clinical trials, ensuring compliance with regulatory requirements, and...Lavoro da remoto
- ...“Personalized response monitoring in oncology: co-creating clinical trials in advanced breast cancer” PREMIO-COLLAB - è un progetto di... ...collaborazione di 10 Centri di eccellenza europea, oltre all'Istituto Clinico Humanitas di Rozzano. E’ un progetto che viene svolto in...
55.000 € - 65.000 €
...Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing... ...cancer research in the clinical trial setting. Our passionate team is committed... ...monitoring early-phase trials Read, write and speak fluent English Completion of a science...Tempo pienoLavoro da casaOrario flessibile- ...Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive... ...ICON, you will support the management and monitor of clinical trial sites by ensuring compliance with study protocols, regulatory requirements...Lavoro da remoto
- ...service CRO with a global reach, supporting clinical trials across multiple countries and continents... ...in the pharmaceutical industry. Job Description As part of PSI's... ...participants Ensure that the reported trial data is accurate, complete, and verifiable...Tempo pieno
- Plan and conduct independent clinical (GCP) audits to assess compliance... ...Italy in accordance with the Italian Decree of the Ministry of... ...Experienced in the conduct of clinical trial Investigator site audits.•... ...a number of factors including job-related qualifications such as...Lingua italianaPart-timeTempo pienoDisponibilità immediata
- Clinical Research AssociateICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new... ...suppliers.As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-...Tempo pieno
- Senior Clinical Research AssociateICON is a global healthcare intelligence and clinical research organisation united by a mission to bring... ...a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol,...Tempo pieno
- Job SummaryOur clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates... ...;Familiarity with Microsoft Office;Fluent in English and Italian language; Strong communication and presentation skills...Lingua italianaTempo pienoLavoro da casaOrario flessibile
33.900 € - 66.700 €
...Job Overview Perform monitoring and site management work to ensure that sites are... ...accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt,... ...are available for filing in the Trial Master File (TMF) and verify that the Investigator...Part-timeTempo pienoDisponibilità immediata- ...Scientific/TechnologyAll Job Posting Locations:Brussels,... ...consistent and optimum clinical outcomes. Provides outcomes... ...J&J products including clinic workflow, patient pre management, pre & post operative checks and... ...Other languages valued (Italian)Position Accountability...Lingua italianaTempo pienoOrario flessibile
32.200 € - 53.400 €
...Experienced Clinical Research Associate, Italy Your responsibilities will include: Performing... ...in Pharma Industry, and/or Clinical Trials environment Very good computer skills... ...based on a number of factors including job-related qualifications such as knowledge,...Part-timeTempo pienoAuto aziendaleDisponibilità immediataOrario flessibile25.000 € - 34.000 €
...services. It is also a market leader in certain areas of genomics, clinical trial support, and contract development and manufacturing in the... ...best-performing stocks in Europe over the past 20 years. Job Description Eurofins Biopharma Product Testing is...Tempo pieno- ...all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development... ...regulatory relevant to drug development, global labeling and post-marketing requirements.Strong scientific background and...Tempo pienoRemoto
- Clinical Research AssociateICON is a global healthcare intelligence and clinical research organisation... ..., you will design and analyse clinical trials, interpreting complex medical data, and... ...Will Do:You will contribute to clinical trial monitoring activities, taking...Tempo pieno
- ...Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to... ...development. As a CRA at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-...Lavoro da remoto
- ...IQVIA is looking for a Senior Clinical Trials Assistant #LI-CES #LI-DNP IQVIA is a leading global provider of clinical research services... ...pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and...Part-timeTempo pienoDisponibilità immediata
33.900 € - 61.700 €
...Job Overview Perform monitoring and site management work to ensure that sites are... ...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference... ...documents are available for filing in the Trial Master File (TMF) verify that the Investigator...Part-timeTempo pienoDisponibilità immediata- Job SummaryThe Clinical Research Associate position at Medpace offers the unique opportunity to have... ...RepresentativeBiomedical/Chemical EngineerPhD/Post-DocPharm.D candidateHealth and... ...DMC 15 /11 / 2011;Fluent in English and Italian language; Strong communication and...Lingua italianaLavoro da casaOrario flessibile
- ...Senior Clinical Reseacrh Associate ICON plc is a world-leading healthcare intelligence... ...ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute... ...Do: You will contribute to clinical trial monitoring activities, taking...Lavoro da remoto
- Job SummaryWe are seeking a Hepatologist to join our team in London. The Medical Director... ...planning, execution, and reporting of clinical trials. Additionally, this role acts as the... ...licensure are preferred;Prior clinical trial research experience preferred; andPrevious...Lavoro da casaLavoro ibridoOrario flessibile
- ...Sr. Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud... ...will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol,...Lavoro da remoto
- ...interpersonal skills Fluency in English and Italian Leadership abilities Proactive,... ...IQVIA is a leading global provider of clinical research services, commercial insights and... ...vary based on a number of factors including job-related qualifications such as knowledge,...Lingua italianaPart-timeTempo pienoDisponibilità immediataOrario flessibile
73.900 € - 125.900 €
...Job Overview The Associate Medical Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions... ...Science involvement on assigned trials. Serve as a medical expert... ...review and clarification of trial-related Adverse Events (AEs)....Part-timeTempo pienoDisponibilità immediata
