
Leading company in the technology industry
Ctry Approval Spec
Work Schedule
Standard Office Hours (40/wk)
Environmental Conditions
Office
Job Description
- Prepares, reviews and coordinates, under guidance, regulatory submissions to EU CTIS ( and additional special national local applications if applicable, e.g. gene therapy approvals) in alignment with global submission strategy;
- Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients;
- May have contact with investigators for submission related activities;
- Key-contact at country level for either Ethical or Regulatory submission-related activities;
- Coordinates, under guidance, with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation;
- Achieves PPD’s target cycle times for site;
- May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable;
- May develop country specific Patient Information Sheet/Informed Consent form documents;
- Enters and maintains trial status information relating to start up activities onto PPD tracking databases in an accurate and timely manner;
- Ensures the local country study files and filing processes are prepared, set up and maintained as per PPD WPDs or applicable client SOPs;
- Maintains knowledge of and understand PPD SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided.
Qualifications:
Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years).
**Working Conditions and Environment: **
- Work is performed in an office/ laboratory and/or a clinical environment.
- Exposure to biological fluids with potential exposure to infectious organisms.
- Exposure to electrical office equipment.
- Personal protective equipment required such as protective eyewear, garments and gloves
閲覧数
0
応募クリック
0
Mock Apply
0
スクラップ
0
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Thermo Fisherについて

Thermo Fisher
PublicThermo Fisher Scientific Inc. is an American life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.
10,001+
従業員数
Waltham
本社所在地
$200B
企業価値
レビュー
10件のレビュー
3.5
10件のレビュー
ワークライフバランス
2.8
報酬
3.2
企業文化
4.1
キャリア
2.9
経営陣
2.7
65%
知人への推奨率
良い点
Great team culture and dynamics
Excellent benefits and health plans
Supportive management
改善点
Heavy workload and frequent overtime
Poor management and lack of direction
Limited advancement opportunities
給与レンジ
2,095件のデータ
Junior/L3
Mid/L4
Senior/L5
Junior/L3 · CLIENT SERVICES PROJECT MANAGER III
1件のレポート
$79,685
年収総額
基本給
$79,685
ストック
-
ボーナス
-
$79,685
$79,685
面接レビュー
レビュー3件
難易度
3.3
/ 5
期間
14-28週間
内定率
33%
体験
ポジティブ 0%
普通 67%
ネガティブ 33%
面接プロセス
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Panel Interview
5
Offer
よくある質問
Behavioral/STAR
Past Experience
Technical Knowledge
Culture Fit
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