Kenvue 目前正在招聘 a：
我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
Global BioStats, Data Mgmt & Prog位置：
Asia Pacific, India, Karnataka, Bangalore工作地點：
混合你會做什麼
Responsibilities will include but not limited to
Plans and manages the design and implementation of Data Management tasks for complex human use research activities to successfully achieve strategic objectives
Ensures all Data Management activities are conducted in accordance with high ethical and quality standards, all applicable GCP regulations and company procedures
Coordinate with Data Management lead in the development of SOPs and other data management standards
Collaborates with other functions such as Clinical and Biostatistics in evaluating and/or implementing opportunities to improve Data Management solutions
Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects
Responsible for end-to-end clinical data management activities and serves as a primary point of contact for internal and external study team members with some oversight from senior data management resources
Provides strong quality and project oversight over third party vendor responsible for data management deliverables
Takes a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (eCOA, External Data)
Enforces data standard conventions and quality expectations for clinical data per defined processes
Contribute to the definition of data structure standards
Authors, reviews/revises DM related study plans including Data Management Plan, Edit Check Specifications, eCRF Completion Guidelines and other study documents to ensure quality and standardization
Chairs Data Quality Review meetings with cross functional study team members to ensure on-going review of clinical study data accuracy, quality and completeness
Represents DM on cross-functional project teams & submission teams
Provides support to Health Authority inspections and audits
Represents Data Management on cross-functional project teams
Evaluates proposals from external service providers
Mentor junior professionals for skill set advancement
FSP/CRO/Vendor Oversight: May act as core member of the study team and provides FSP/CRO/Vendor oversight for end-to-end Data Management activities, manages data currency throughout the trial, and overall monitoring DM deliverables according to the Service Level Agreement (SLA)
Required Qualifications & Core Competencies
Bachelor’s Degree in Mathematics, Science or a related field required
At least 8 years of clinical data management experience in healthcare related industry
Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors
Sound knowledge of all applicable regulations including CFR, GCP, ICH guidelines and industry standard practices regarding data management
Proficiency with Clinical Data Management System required
Strong project management; Exhibits expertise in metrics analysis and reporting methodologies
Strong oral and written communication skills
Communicate effectively with senior management and cross-functional teams
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