Field Trainer, Northeast
Dandy$82,100 - $95,000/year
Full Time
Mid-level (3 to 4 years), Senior (5 to 8 years)
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Part TimeJob Type
UnknownVisa
Clinical Research, Healthcare, PharmaceuticalIndustries
Requirements
- Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred
- 3+ years administering psychiatric assessments, rating scales, and structured clinical interviews (including EQ-5D-5L – Interviewer administered and Proxy 1 version, and smRS)
- 3+ years of clinical experience with psychiatric populations
- 3+ years administering scales in clinical research trials (excluding graduate/doctoral work)
- CNS trial experience is a plus
- Strong interpersonal and communication skills for professional interaction at all levels
- Excellent organizational skills, attention to detail, and time management
- Proficiency with Windows and Microsoft Office applications
- Fluency in English and native-level proficiency in Tamil
Responsibilities
- Participate in orientation, training, and calibration activities
- Review case data and prepare for rater discussions with all necessary documentation
- Conduct scheduled rater interactions and provide guidance on scoring techniques and methodology
- Complete assigned tasks and submit documentation accurately and on time
Skills
Key technologies and capabilities for this role
Questions & Answers
Common questions about this position
Is this position remote?
Yes, the position is remote/virtual with a flexible work schedule.
What are the education and experience requirements?
A Master’s degree in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent) is required, with MD, DO, or PhD preferred. Candidates need 3+ years administering psychiatric assessments and rating scales, 3+ years of clinical experience with psychiatric populations, and 3+ years administering scales in clinical research trials.
What language skills are required?
Fluency in English and native-level proficiency in Tamil are required.
How many hours per month is this part-time role?
The role is estimated at 10–16 hours per month.
What skills make a strong candidate for this role?
Strong interpersonal and communication skills, excellent organizational skills with attention to detail, time management, and proficiency with Windows and Microsoft Office are key. Experience in CNS trials is a plus.
IQVIA
Advanced analytics and clinical research services
About IQVIA
IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.
Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees
Risks
Rapid advancement of cancer vaccines may disrupt traditional clinical research models.
Proliferation of disparate technological solutions causes technology overload in clinical trials.
Generative AI technologies face challenges in adoption due to data privacy concerns.
Differentiation
IQVIA leverages advanced analytics and big data for life sciences solutions.
The company offers privacy-enhancing technologies to protect individual patient data.
IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.
Upsides
Increased adoption of decentralized clinical trials enhances patient-centric study designs.
AI-driven drug discovery accelerates identification of potential drug candidates.
Expansion of telemedicine facilitates remote patient monitoring and data collection.
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