Position : Senior Clinical Documentation Coordinator
Location : Lansdale, PA (Hybrid)
Duration : 2 months
Job Overview :
The Senior Documentation Coordinator will oversee the management and organization of procedural documents, offering guidance on documentation strategies within the Global Regulatory Affairs and Clinical Safety (GRACS) department.
The role also involves close collaboration with cross-functional teams to ensure that the documentation accurately reflects current processes and adheres to regulatory requirements.
Key Responsibilities :
- Manage the lifecycle of procedural documents, from development through to approval and final implementation, ensuring they meet organizational standards.
- Lead assessments to determine the impact of process updates across the full document library, providing insights to streamline the revision process.
- Collaborate with team leads and subject matter experts to create and update process flows that support efficient documentation development.
- Ensure the documentation is regularly reviewed and updated to align with organizational standards for format, structure, and style.
- Facilitate the smooth execution of documentation revisions by supporting change control systems and ensuring timely access for team members.
- Coordinate document retrieval and management requests for internal audits and compliance reviews.
Qualifications :
- Bachelor's degree or higher.
- At least 6 years of relevant industry experience with a focus on procedural documentation within regulatory or safety functions.
- Strong understanding of managing documentation for regulatory or pharmacovigilance processes.
- Familiarity with content organization and control systems for ease of access and retrieval.
- Preferred experience with Veeva Vault or similar document management tools.
Senior Clinical Documentation Coordinator - DS24-13657
The Senior Documentation Coordinator will oversee the management and organization of procedural documents, offering guidance on documentation strategies within the Global Regulatory Affairs and Clinical Safety (GRACS) department. Senior Clinical Documentation Coordinator. The role also involves clos...
Senior Clinical Research Coordinator
As a result, we are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief employee) to support our mission and our clients’ mission to impact and save lives. Minimum of 2 or more years of experience in clin...
Clinical Documentation Specialist - CDS24-13657
The Documentation Specialist - III (Senior) will support the operational aspects of procedural documentation management and advise on documentation strategy within the Global Regulatory Affairs & Clinical Safety (GRACS) organization. Clinical Documentation Specialist . Support and manage re...
Research Investigator/Sr. Research Investigator/Associate Director, Clinical Pharmacology and Pharma
The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. The CP&P team interacts with discovery and translational scientists, project leadership, early and la...
Nurse Coordinator - Trauma Program
Are you ready to take your nursing career to the next level while making a meaningful impact in one of New York's premier healthcare systems? A highly reputable 400+ bed acute care hospital system in the heart of New York, is searching for a dynamic Nurse Coordinator for their Trauma Program. A...
Research Assistant
The Research Assistant position will involve measuring the beam steering capability of our newly fabricated photonic device. ...
Senior Clinical Research Associate
Budgeting, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems (CTMS), Clinical Trials, Clinical Trials Monitoring, Communication, Data Analysis, Decision Making, Financial Analysis, Health Sciences, Life Science. Excellent knowledge of the drug development process specifica...
APC Manager - Clinical Services - New Jersey - Optum
In collaboration with the DCO, the Senior CSM will strategize, develop, and direct operations of the clinical department to ensure the provision of high quality and cost-effective medical services are delivered to membership. In collaboration with DCO develops well-designed processes, which will be ...
Sr. Manager, Pharmacy Support Services
Partners with the CDSL Managers, the Formulation Development Group (FDG), Regulatory Sciences (RS)/ Affairs (RA), as well as members of the Clinical Trial Management team (CTM) including the Clinical Study Lead (CSL), Study Medical Director (SMD) and Clinical Scientist (CS), Quality Management Lead ...
Research Investigator/Sr. Research Investigator/Associate Director, Clinical Pharmacology and
Those aren't words that are usually associated with a job. For Associate Director level with Ph. Research Investigator, with Ph. For Research Investigator, with Ph. ...