Job Title: Medical Project Coordinator
Experience Required: 2+ years
Job Type: Full-time
Location: Remote, India
Department: Clinical Research Services
Function: Pharmacovigilance / Medical Monitoring
Job Description:
Functional Role:
Medical Project Coordinator – Clinical Safety & Pharmacovigilance
Department:
Clinical Research Services (PPD® Portfolio)
Reporting To:
Medical/Project Management Leadership
Location:
Fully Remote (India)
Primary Responsibilities:
Coordinate and manage safety data activities using dashboards, line listings, and visualization tools to track trends and coding consistency.
Review safety data and provide summaries or inputs for safety review meetings and aggregate safety reports.
Assist in drafting or reviewing safety and medical management plans to align with contract scope and study protocols.
Manage routine aspects of clinical project execution, such as progress tracking, forecasting, and budget metrics.
Identify and escalate issues in data review, working collaboratively with study leads and stakeholders.
May act as the primary contact for project teams including clinical and data management.
Participate in business development meetings, client briefings, and investigator interactions.
Contribute to mentoring and training of junior team members as needed.
Education and Experience:
Bachelor’s degree in Nursing, Health Sciences, or Physician Assistant. Registered Nurse (RN) license preferred.
Minimum of 2 years of experience in clinical safety, pharmacovigilance, or clinical research monitoring.
Strong familiarity with GCP guidelines, SAE processing, and clinical development lifecycle.
Experience with safety data review, coding, and trending highly preferred.
Knowledge, Skills, and Abilities:
Strong analytical and critical thinking abilities with a focus on problem resolution.
In-depth understanding of clinical safety reporting standards and data quality principles.
Knowledge of drug development processes, biostatistics, and data management practices.
Proficiency in safety review tools and standard office technologies.
Strong verbal and written communication skills.
Ability to manage multiple priorities under deadlines in a collaborative environment.
Professional demeanor with resilience in challenging scenarios.
Work Environment:
Standard (Mon-Fri) work schedule; remote setup.
Office-based environmental conditions.
Occasional travel may be required.
What We Offer:
Career advancement opportunities in global clinical research.
Flexible work culture and remote working model.
Comprehensive benefits with focus on employee wellness and development.
Engaging team environment with strong emphasis on learning and innovation.
Gujarat :
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Japan | Saitama |Tokyo :
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Kyiv |Lima Region :
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