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Fortrea

Global CRO providing Phase I-IV trials

Medical Contact Center Associate 1

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeManila, Metro Manila, PhilippinesNo salary listed

About the Job

Requirements

  • A bachelor's or master's degree in Pharmacy, Life Science, Medical Science, or a related area, plus 1 to 2 years of safety experience; alternatively, a BS/BA plus 1 to 2 years of safety experience, an MA/MS/PharmD plus 1 to 2 years of safety experience, an associate degree plus 3 to 4 years of relevant experience or 2 years of safety experience, or no degree plus 4 to 5 years of relevant experience or 2 years of safety experience. Fortrea may consider relevant and equivalent experience instead of educational requirements.
  • Safety experience includes processing adverse event or serious adverse event reports, generating narratives and queries, working within safety databases, and experience with regulatory submissions.
  • Relevant experience includes pharmaceutical, biotechnology, or contract research organization industry experience, including related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance.
  • Good written and verbal communication skills.
  • Ability to receive and manage inbound and outbound calls.
  • Ability to analyze and synthesize medical information.
  • Good understanding of regulatory requirements, good Pharmacovigilance practices, and International Council for Harmonisation Good Clinical Practice guidelines.
  • Technical proficiency with Microsoft Office suite applications.
  • High degree of accuracy and attention to detail.
  • Ability to work independently with moderate supervision.

Responsibilities

  • Respond to medical information queries, product quality complaints, and general queries received by telephone, email, fax, or other channels.
  • Receive information, record, and report adverse drug reactions within required timelines according to regulations and internal work instructions and standard operating procedures.
  • Execute drug safety data management processes, including call intake, call dialogue documentation, peer review, and case follow-up.
  • Perform and support assigned activities, including tracking information and metrics, ongoing quality control of defined process steps, training, and reconciling data from multiple sources.
  • Assume responsibility for the quality of processed data.
  • Perform other duties as needed or assigned.

Desired Qualifications

  • A degree in one or more of the following disciplines is preferred but not required: Biological Sciences, Pharmacy, Nursing, Life Sciences, or Chemistry.
  • Experience in a call center process is preferred.

About the Company

Fortrea

Global CRO providing Phase I-IV trials

Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.

Company size
10,001+
Company stage
IPO
Headquarters
Winston-Salem, NC
Founded
2023

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