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Clinical Systems Coordinator-2507030214w

3+ years
Not Disclosed
10 Feb. 6, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

### **Clinical Systems Coordinator - 2507030214W**  
📍 **Location:** Bangalore, Karnataka, India  
🗓️ **Posted:** [Date not specified]

#### **About Kenvue:**
At Kenvue, we are a global leader in consumer health and personal care, with a rich history of iconic brands such as NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S®, and BAND-AID®. Our mission is to harness the extraordinary power of everyday care to improve the lives of millions of people around the world. We’re passionate about science, care, and innovation. If you share our vision, join us in shaping a better, healthier future.

#### **What You Will Do:**
The **Clinical Systems Coordinator** will support the global clinical operations systems and processes, including training programs, system administration, and ensuring compliance with Good Clinical Practices (GCP). This position will work closely with Clinical Operations, Study Managers, Clinical IT, and other stakeholders to maintain clinical systems such as CTMS (Clinical Trial Management System) and eTMF (electronic Trial Master File).

#### **Key Responsibilities:**
- Support the maintenance and optimization of Clinical Operations’ systems.
- Collaborate on the creation and optimization of training programs related to clinical systems.
- Act as a backup Clinical Business Administrator for system-related activities including CTMS and eTMF administration.
- Monitor and ensure adherence to Clinical Operations policies and SOPs to maintain inspection readiness.
- Assist in identifying process challenges and suggest technology-driven improvements.
- Contribute to project plans and system-related activities.
- Identify system issues and escalate them for resolution.
  
#### **Qualifications:**

**Required:**
- **Education:** Bachelor’s degree in science, nursing, or related field.
- **Experience:** Minimum 3 years of experience in a Clinical Study Manager role or related GCP procedures work.
- **Skills:**
  - Prior experience with clinical systems such as CTMS and eTMF.
  - Proficiency in ICH GCP regulations and Microsoft Office applications.
  - Excellent communication and presentation skills in English.
  - Strong attention to detail and problem-solving abilities.
  - Ability to work with global teams in a dynamic and agile environment.

**Desired:**
- Exposure to GCP regulatory inspections and Change Management methodologies.

#### **What’s In It For You:**
- Competitive benefit package.
- Paid company holidays, vacation time, volunteer opportunities, and more.
- Learning and development opportunities.
- Employee Resource Groups.

#### **How to Apply:**
To submit your application, please upload your CV and cover letter as instructed.

**Slug:** *clinical-systems-coordinator-2507030214w*