Job Description

eTrial Master File Senior Analyst
Job Number: 21-02064
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for an eTrial Master File Senior Analyst for our client in Lawrenceville, NJ
 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Position Overview:
  • To deliver technical expertise in the Electronic Trial Master File (eTMF), provide support for all clinical trials throughout the lifecycle of the trial and what is in the book of work, and support inspection readiness goals in compliance with ICH/GCP guidelines
  • Work closely with Global Trial Managers and TMF Study Leads to support the completeness of the TMF
 
Responsibilities:
  • Ensuring accuracy at the document level in the eTMF for all Client-managed studies and CRO-managed studies in the Client eTMF, with the study teams and TMF Study Leads, Global Trial Managers and/or Subject Matter Experts for eTMF
  • Monitor the adherence to ICH/GCP Guidelines, regulatory requirements, ALCOA+ Principles and Client policies as it relates to the completeness and accuracy of the TMF at the document level
  • Ensure that the documents are filed in the correct classification and that the required metadata is accurate and complete in the TMF as per the Study-Specific Master Plan and Master List and are inspection ready at all times
  • Manage complex and more technical tasks within the eTMF; including but not limited to: template creation and management, controlled document templates, system hard deletion process, creating complex ad hoc TMF reports for users, developing custom reports to generate metrics, developing or enhancing macros to streamline existing and new processes
  • Demonstrates ability to make decisions, deliver on commitments, share knowledge, acknowledge others achievements, and collaborate with peers in order to meet objectives or timelines in a rapidly changing environment
  • Exhibit knowledge of critical and essential documents to be able to perform Quality Validation checks on documents that have had completed quality review
  • Ability to make sound business decisions based on evidence (guidance documents and Manual of Operations) and experience regarding the outcome of the eTMF work that is performed that involves critical or complex documents
  • Generate, organize, and deliver performance metrics for various functional areas within eTMF Operations
  • Leverage interpersonal and influencing skills to foster partnerships across multidisciplinary teams
  • Assist in overall change management and build collaborative relationships with cross-functional team and third-party vendors
  • Participate in reviewing and updating documents to ensure that they are reflective of industry standards, applicable regulations and are easily retrieved following a regulatory inspection
  • Exhibit good project management skills that include working closely with the study teams to achieve goals and meet success criteria within specified timelines
  • Display good time management skills, the ability to produce deliverables efficiently, meet timelines, and prioritize workload to meet business goals
  • Provide support to TMF implementation, internal audits and regulatory inspections
  • Demonstrate ability to make decisions, deliver on commitments, share knowledge, acknowledge others achievements, and collaborate with peers in order to meet objectives or timelines in a rapidly changing environment.
 
Qualifications:
  • Minimum of Bachelor’s degree in a scientific or related discipline
  • At least 5 years of TMF experience required, including experience in study start-up, study maintenance and document quality reviews
  • Relevant experience in clinical trials related roles (i.e. clinical operations and project management)
  • Previous experience with independently managing projects and handling concurrent tasks in a fast-paced environment and delivering results within tight timelines
  • Critical thinker: Utilizing an intellectually disciplined process of actively and skillfully conceptualizing, applying, analyzing, synthesizing and/or evaluating information gathered from, or generated by, experience, reasoning or communication that will be instrumental in the decision-making process for quality review
  • Demonstrated working knowledge of the pharmaceutical industry including ICH/GCP guidelines
  • Experience managing clinical content in a records management system or electronic Trial Master File system
  • Very strong communication skills, verbal and written
 
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
 
If interested, you may contact:
Maria Castañeda
maria.castaneda@eclaro.com
6463571235
Maria Castañeda | LinkedIn
 
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status

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