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Pspm Senior Support Associate

5+ years
Not Disclosed
10 Oct. 24, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

As a leading global contract research organization (CRO), Fortrea is dedicated to scientific rigor and brings decades of clinical development experience. We provide a comprehensive range of clinical development, patient access, and technology solutions to pharmaceutical, biotechnology, and medical device customers across more than 20 therapeutic areas. With over 19,000 staff operating in more than 90 countries, Fortrea is transforming the development of drugs and devices for partners and patients worldwide.


Job Description:

  • Report Management: Ensure the efficiency and accuracy of reports and dashboards.
  • PowerPoint Automation: Develop MS PowerPoint automations to analyze trends, performance, and actions for management.
  • Data Analysis: Analyze data trends to provide actionable insights.
  • Report Accuracy: Ensure the accuracy and timeliness of reports.
  • Collaboration: Work with various departments to gather and analyze data.
  • Tool Implementation: Implement reporting tools and dashboards for enhanced data visualization.
  • Independent Work: Ability to work independently with meticulous attention to detail.
  • Analytical Skills: Strong analytical and coordination skills.
  • Relevant Experience: Experience in management reporting and analysis.
  • MIS Development: Design, develop, and maintain MIS systems to meet organizational needs.
  • Technical Knowledge: Knowledge of PowerBI & SQL is an added advantage.

Support Responsibilities:

  • Assist with the setup, maintenance, and closeout of global or regional projects in clinical trials and post-marketing studies.
  • Support the Global Safety lead in preparing Safety Management Plans (SMPs), Reconciliation Plans, and other safety-specific plans.
  • Help prepare study-specific job aids, instructions, training, and templates.
  • Support system setups during study startups and ongoing maintenance.
  • Assist in project-specific functional management and financial management tasks.
  • Generate monthly status and other project-specific reports ensuring quality and accuracy.
  • Assist with Trial Master File (TMF) management and compliance with safety reporting regulations.
  • Maintain a comprehensive understanding of Fortrea’s safety database conventions and standard operating procedures (SOPs).

Experience Required:

  • 5+ years of relevant experience in MIS, preferably from a CRO background.

Education Background:

  • Bachelor’s or Master’s degree (preferably in a life science field).

Location:

  • Bangalore

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing therapies to patients in need. Join our exceptional team and thrive in a collaborative environment that nurtures personal growth, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Equal Opportunity Employer:

Fortrea is proud to be an Equal Opportunity Employer (EOE/AA) that values diversity and inclusion. We do not tolerate harassment or discrimination and make employment decisions based on business needs and individual qualifications. We encourage all qualified individuals to apply.

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