Clinical Trial Psych Rater

6 days ago


Bengaluru, Karnataka, India IQVIA Full time ₹ 1,04,000 - ₹ 1,30,878 per year

Clinical Specialist Consultant - Malayalam Speaking

 

Location:  Remote/virtual

Hours:  Estimated 10-16h/month

Role:  Clinical Specialist

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-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



  • Bengaluru, Karnataka, India IQVIA Full time ₹ 1,04,000 - ₹ 1,30,878 per year

    Clinical Specialist Consultant - Oriya Speaking Location:  Remote/virtualHours:  Estimated 10-16h/monthRole:  Clinical SpecialistJob 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...


  • Bengaluru, Karnataka, India beBeeDermatologist Full time ₹ 1,00,00,000 - ₹ 2,00,00,000

    Clinical Trials Dermatologist Role OverviewAs a skilled Clinical Trials Dermatologist, you will play a pivotal part in the success of our dermatology-focused clinical trials. Your expertise in medicine and dermatology will enable you to conduct clinical trials as an investigator or co-investigator, performing dermatological evaluations for diagnosing and...


  • Bengaluru, Karnataka, India beBeeCustomerSupport Full time US$ 80,000 - US$ 1,20,000

    Job DescriptionWe are seeking a highly motivated and organized Research Associate to join our team. The ideal candidate will have excellent communication skills, be highly personable, and possess a passion for ensuring outstanding customer support.Understand and interpret clinical trial study protocols to design and develop calendars.Design and develop case...


  • Bengaluru, Karnataka, India beBeeScientific Full time ₹ 15,00,000 - ₹ 25,00,000

    Job OverviewDevelop high-quality clinical trial documents, including protocols and study reports.Translate complex scientific data into clear, regulatory compliant documents.Key Responsibilities:Create key clinical trial documents such as protocols, investigator's brochures, informed consent forms, case report forms, and clinical study reports.Communicate...


  • Bengaluru, Karnataka, India beBeeClinicalOperations Full time ₹ 1,04,000 - ₹ 1,30,878

    Job Title: Associate Clinical LeadOur organization is seeking a highly skilled and experienced Clinical Operations Manager to lead and oversee clinical trial activities. This key role will be responsible for ensuring that trials are conducted according to protocols and regulations, managing clinical trial staff and resources, reviewing and approving trial...


  • Bengaluru, Karnataka, India MS CLINICAL RESEARCH Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...


  • Bengaluru, Karnataka, India beBeeData Full time ₹ 8,00,000 - ₹ 15,00,000

    Statistical Data Analyst RoleThis role combines statistical knowledge with programming skills to drive clinical research forward.Key Responsibilities:Contribute to dataset development and statistical output creation for clinical trial reportingAssist in producing key statistical outputs used in clinical trial documentationReview AI-generated statistical...


  • Bengaluru, Karnataka, India beBeeclinical Full time

    Job SummaryThis role is responsible for supporting the management of clinical trials in Japan. The successful candidate will have experience with document collection, customization, and review, as well as knowledge of clinical trial documentation, processes, and systems.">\


  • Bengaluru, Karnataka, India beBeeMonitoring Full time ₹ 80,00,000 - ₹ 1,60,00,000

    Job Overview:Centralized Monitoring LeadAs Centralized Monitoring Lead, you will be responsible for providing strategic leadership to a team of professionals in achieving project objectives. Your expertise will ensure the efficient review of site visit reports and consistent quality standards.This role requires a strong understanding of clinical trial...


  • Bengaluru, Karnataka, India beBeeStatistical Full time ₹ 1,00,00,000 - ₹ 1,40,00,000

    Job Title: Statistical ProgrammerJob Description:We are seeking a skilled Biostatistician cum Statistical Programmer to join our team. As a key member of our cross-functional team, you will be responsible for performing biostatistical and SAS programming activities for clinical trials involving novel, biosimilar, and PMS studies.Your primary responsibilities...