採用

Clinical Trial Psych Rater - Malay
Wilayah Persekutuan Kuala Lumpur, Malaysia
·
On-site
·
Contract
·
2mo ago
必須スキル
Psychiatric assessment administration
Rating scale administration
Structured clinical interviews
Interpersonal communication
Organization
Attention to Detail
Time Management
Problem-Solving
Clinical Specialist Consultant - Malay 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:
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Minimum of a master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing or Social Work, or equivalent. MD, DO or PhD preferred
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Minimum of 3 years’ experience administering psychiatric assessments, ratings scales and/or structured clinical interviews. Specifically, EQ-5D-5L (Interviewer administered and Proxy 1 version) & smRS
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Minimum of 3 years clinical experience with related psychiatric populations.
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Minimum of 3 years experience with administering scales in clinical research trials (not including graduate/doctoral research work).
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Experience in central nervous system (CNS) trials preferred.
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Strong interpersonal skills with ability to interact with all levels of personnel and clientele in a professional manner.
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Excellent organization, attention to detail, time management and problem-solving skills.
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Computer proficiency with Windows and Microsoft Office system and applications.
Tasks/Responsibilities:
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Participate in all orientation, training and calibration activities as required.
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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).
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Complete rater interactions and assigned tasks as scheduled.
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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.
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 https://jobs.iqvia.com
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IQVIAについて

IQVIA
PublicIQVIA Holdings, Inc. is an American company based in Durham, North Carolina, focused on health information technology and clinical research.
10,001+
従業員数
Durham
本社所在地
$17B
企業価値
レビュー
3.6
10件のレビュー
ワークライフバランス
3.8
報酬
2.5
企業文化
4.0
キャリア
3.2
経営陣
2.8
65%
友人に勧める
良い点
Good work-life balance
Supportive team and collaborative environment
Good benefits and flexible hours
改善点
Compensation below industry standards
High workload and overwhelming at times
Management communication and organization issues
給与レンジ
45件のデータ
Junior/L3
Senior/L5
Junior/L3 · Analyst
2件のレポート
$107,910
年収総額
基本給
$93,834
ストック
-
ボーナス
-
$97,750
$118,068
面接体験
3件の面接
難易度
3.0
/ 5
期間
14-28週間
体験
ポジティブ 0%
普通 33%
ネガティブ 67%
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Technical Manager Interview
5
Executive/GM Interview
6
Offer
よくある質問
Behavioral/STAR
Case Study
Technical Knowledge
Past Experience
Culture Fit
ニュース&話題
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5d ago
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1w ago