
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
전체 조회수
0
전체 지원 클릭
0
전체 Mock Apply
0
전체 스크랩
0
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Thermo Fisher 소개

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+
직원 수
Waltham
본사 위치
$200B
기업 가치
리뷰
10개 리뷰
3.5
10개 리뷰
워라밸
2.8
보상
3.2
문화
4.1
커리어
2.9
경영진
2.7
65%
지인 추천률
장점
Great team culture and dynamics
Excellent benefits and health plans
Supportive management
단점
Heavy workload and frequent overtime
Poor management and lack of direction
Limited advancement opportunities
연봉 정보
2,095개 데이터
Junior/L3
Mid/L4
Senior/L5
Junior/L3 · CLIENT SERVICES PROJECT MANAGER III
1개 리포트
$79,685
총 연봉
기본급
$79,685
주식
-
보너스
-
$79,685
$79,685
면접 후기
후기 3개
난이도
3.3
/ 5
소요 기간
14-28주
합격률
33%
경험
긍정 0%
보통 67%
부정 33%
면접 과정
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Panel Interview
5
Offer
자주 나오는 질문
Behavioral/STAR
Past Experience
Technical Knowledge
Culture Fit
최근 소식
Building quality into drug development for safer, faster medicines - News-Medical
News-Medical
News
·
1w ago
Thermo Fisher Refocuses On Biopharma With Microbiology Sale And New Center - simplywall.st
simplywall.st
News
·
1w ago
Thermo Fisher Scientific to Host Investor Day - April 28, 2026 - BioSpace
BioSpace
News
·
1w ago
Thermo Fisher opens new facility for vaccine, gene therapy development - The Boston Globe
The Boston Globe
News
·
1w ago