Safety Data Lead I
4 weeks ago
Job Description
The Safety Data Lead I is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a GPVCM Manager, the Safety Data Lead executes AE case management activities for both investigational and marketed products in accordance with specific therapeutic area standards. Collaboration with internal and external stakeholders is essential to maintain high quality and timely execution of the processes.
Among other tasks, the Safety Data Lead is responsible for:
- Performing analysis, interpretation, and data entry of adverse event reports from a wide range of sources and therapeutic areas, demonstrating increasing proficiency in clinical knowledge, GPVCM processes and regulatory guidelines.
- Providing support or leading operational activities appropriate to level of experience and expertise.
- Collaborating with internal and external stakeholders to resolve issues of varying complexity to guarantee process standardization and adherence and ensure compliance with reporting requirements.
- Supporting simplification and optimization of case management activities to enhance overall effectiveness.
#Global Data Management Standard
Current Employees apply HERE
Current Contingent Workers apply HERE
Secondary Language(s) Job Description:
Education and other Qualifications:
- Bachelor’s degree or above in health care or life sciences disciplines.
- Advanced writing/reading and intermediate speaking/listening English language skills.
- Optional advanced writing/reading and intermediate speaking/listening other region-specific language skills.
- Understanding of pharmacovigilance-related regulations is desired.
Core Competencies:
- Decision Making: identifying and understanding problems and opportunities by gathering, analyzing, and interpreting quantitive and qualitive information; choosing the best course of action by establishing clear decision criteria, generating, and evaluating alternatives, and making timely decisions.
- Business Savviness: understanding the business; building and applying knowledge of company and functional area operations, to improve individual, work group and/or organizational results.
- Networking & Partnerships: building partnerships; developing and leveraging relationships within and across work groups to achieve results.
- Strategic Planning: prioritizing and planning; establishing an action plan for self and others to complete work efficiently and on time by setting priorities, establishing timelines, and leveraging resources.
- Motivation and Inspiration: Communicating effectively; conveying information and ideas clearly and concisely to individuals or groups in an engaging manner that helps them understand and retain the message; listening actively to others.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
No Travel RequiredFlexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
N/AJob Posting End Date:
07/1/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R315725
-
Safety Data Lead I
1 month ago
Beijing, China MSD Full timeJob DescriptionThe Safety Data Lead I is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes. Working under the supervision of a Global Pharmacovigilance Case Management (GPVCM) Manager, the Safety Data Lead I executes AE case management...
-
Clinical Research Associate I
2 weeks ago
Beijing, Beijing, China Parexel Full timeJob Summary: We are seeking a skilled Clinical Research Associate I (FSP) to join our team at Parexel.About the Role:Conduct Source Data Verification and Ensure Clinical Trials Data are Submitted in a Timely Fashion: The successful candidate will be responsible for conducting source data verification (SDV) and ensuring that clinical trials data are submitted...
-
Regional Safety Engineer
6 months ago
Beijing, China Amazon Connect Technology Services (Beijing) Co., Ltd. Full timeOverviewThis role is for an experienced EHS Manager, Health and Safety Specialist or Engineer. The role's prime responsibility will be to support the safety operations in the Beijing region. As well as this there may be opportunities to support other regions or countries. The chosen person must be an effective communicator, sending clear, concise and...
-
Map Data Quality Engineer
4 weeks ago
Beijing, Beijing, China Data Annotation Full timeJob Title: Perfect EngineerJob Summary:We are seeking a highly skilled Map Data Quality Engineer to join our team at Data Annotation. As a key member of our team, you will be responsible for ensuring the quality of high-precision map data used in automated driving applications.Key Responsibilities:Quality control of high-precision map data to ensure optimal...
-
Clinical Research Associate I(FSP) Coordinator
2 weeks ago
Beijing, Beijing, China Parexel Full timeUnlocking Success in Clinical ResearchOur team at Parexel is dedicated to delivering exceptional results in clinical trials. As a Clinical Research Associate I(FSP), you will play a critical role in ensuring the success of our studies.Key Responsibilities:Source Data Verification and Data Management Conduct thorough source data verification and ensure timely...
-
Clinical Research Associate I(FSP)
4 weeks ago
Beijing, Beijing, China Parexel Full timeParexel's Clinical Research Associate I(FSP) RoleAs a Clinical Research Associate I(FSP) at Parexel, you will play a critical role in the success of our clinical trials. Your primary responsibility will be to ensure the smooth execution of studies at investigator sites, ensuring that all regulatory requirements are met and that data quality is maintained.Key...
-
Lead Technical Program Manager
9 hours ago
Beijing, Beijing, China NTT DATA Full timeCompany OverviewNTT DATA, a leading technology services company, is seeking an exceptional Lead Technical Program Manager to join our team.
-
Product Safety Manager
2 months ago
Beijing, China Novo Nordisk AS Full timeAre you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment. Apply now and join Novo Nordisk. Together we can create life-changing innovation. Together we can make it...
-
Lead Map Optimization Specialist
9 hours ago
Beijing, Beijing, China Data Annotation Full timeAbout Data AnnotationData Annotation changes the way we drive, from preventing accidents to semi and fully autonomous vehicles. As a leader in map products and technologies, we are constantly pushing the boundaries of innovation.Job DescriptionThe role of Lead Map Optimization Specialist is a critical position within our team, responsible for identifying and...
-
Clinical Research Associate I(FSP)
1 month ago
Beijing, Beijing, China Parexel Full timeJob SummaryParexel is seeking a highly skilled Clinical Research Associate I(FSP) to join our team. As a key member of our site management team, you will be responsible for ensuring the smooth conduct of clinical trials at investigator sites.Key ResponsibilitiesSource Data Verification and Data Management: Conduct source data verification (SDV) and ensure...
-
Technical Project Manager
4 weeks ago
Beijing, Beijing, China NTT DATA Full timeJob OverviewAs a Technical Project Manager, you will be responsible for leading the development of our core platform, ensuring high performance, maintainability, and documentation of our code base. You will work closely with the development team and clients to manage projects, provide technical input, and drive the development of scalable and cost-effective...
-
Senior Technical Program Lead
2 weeks ago
Beijing, Beijing, China NTT DATA Full timeJob Title: Technical Project ManagerJob Summary:As a Technical Project Manager at NTT DATA, you will be responsible for overseeing the technical aspects of our core platform, including the backend of our web application. You will work closely with the development team and clients to ensure the successful delivery of projects.Key Responsibilities:Manage the...
-
SSG Sales Operations Data Foundation Specialist
1 month ago
Beijing, Beijing, China Lenovo Full timeData Foundation and Business Intelligence RoleWe are seeking a highly skilled Data Foundation and Business Intelligence professional to join our team at Lenovo. The successful candidate will be responsible for developing and maintaining data foundations and business intelligence solutions for our SSG organization.Key Responsibilities:Develop and maintain...
-
SSG Sales Ops Data Fundation
4 months ago
Beijing, China Lenovo Full timeDescription and Requirements 1. ISU data foundation and BI (Pipeline, TCV, Bookings, TCV to Bookings) 2. AI Powered Vertical solution data foundation and BI (Pipeline, TCV, Bookings, TCV to Bookings) 3. Project Accounting data foundation and BI (track projects P&L, especially for revenue; revenue vs quotation/accepted final pricing) 4. Take lead...
-
Product Safety Manager
2 months ago
Beijing, China Novo Nordisk Full timeAre you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment. Apply now and join Novo Nordisk. Together we can create life-changing innovation. Together we can...
-
Drug Safety Coordinator
4 weeks ago
Beijing, Beijing, China Parexel Full timeJob SummaryParexel is seeking a highly skilled Drug Safety Assistant to join our team. As a key member of our safety team, you will be responsible for ensuring the integrity and quality of our safety data.ResponsibilitiesTriage and Data Entry: Triage incoming reports for completeness, legibility, and validity, and perform initial data entry of case reports...
-
SSG Sales Operations Data Foundation Specialist
3 weeks ago
Beijing, Beijing, China Lenovo Full timeData Foundation and Business Intelligence ExpertiseWe are seeking a highly skilled Data Foundation and Business Intelligence Analyst to join our SSG team. The ideal candidate will have expertise in building and maintaining data foundations and business intelligence solutions, with a focus on pipeline, TCV, bookings, and TCV to bookings analysis.Key...
-
Health, Safety and Environment Leader
4 weeks ago
Beijing, Beijing, China Cummins Inc. Full timeJob Summary:We are seeking a highly skilled Health, Safety and Environment Leader to join our team at Cummins Inc. This role will be responsible for implementing and sustaining a positive health, safety and environmental culture across our sites with low complexity.Key Responsibilities:Develop and implement health, safety and environmental policies and...
-
Drug Safety Specialist
1 month ago
Beijing, Beijing, China Parexel Full timeJob SummaryParexel is seeking a highly skilled Drug Safety Assistant to join our team. As a key member of our safety services team, you will be responsible for ensuring the highest level of quality and compliance in our safety reporting processes.ResponsibilitiesTriage and Data Entry: Triage incoming reports for completeness, legibility, and validity, and...
-
Clinical Trials Coordinator I
2 weeks ago
Beijing, Beijing, China BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Full timeJob Summary: We are seeking a highly organized and detail-oriented Clinical Trials Coordinator I to support the day-to-day operations of our clinical trials. The successful candidate will provide administrative support to the project team, ensuring timely and accurate completion of tasks.Key Responsibilities:Document and track study activities using relevant...