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Parexel

End-to-end clinical trials and regulatory consulting

Intern

Clinical Research OperationsConfirmed live in the last 24 hours
InternshipManila, Metro Manila, PhilippinesNo salary listedIn-person

About the Job

Requirements

  • Strong computer skills, including knowledge of Microsoft Office products such as Excel and Word.
  • Good organizational skills, ability to manage multiple tasks, and meticulous attention to detail.
  • Maintain a basic knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, and applicable Parexel procedures.
  • Strong command of written and spoken English; local language proficiency as required.
  • Proficient computer and internet skills, including knowledge of Microsoft Office products such as Excel, Word, PowerPoint, Outlook, and WebEx, are advisable.
  • Undergraduate of any Life Sciences degree.

Responsibilities

  • Contribute to site activation by assisting with building the Investigator Site File (ISF).
  • Customize study-specific forms and site templates, including headers and site details.
  • Coordinate local printing of the Investigator Site File when approved by the Study Team.
  • Assist with domestic shipment of materials and equipment to sites.
  • Support site maintenance and inspection readiness by assisting the CRA and COA with scanning and collecting study documents from the site for uploading to the Trial Master File (TMF) by the CRA or COA.
  • Support investigator payment management by reviewing and updating the payment tracker required by Mazars for monitoring Parexel tax compliance.
  • Observe during CRA site visits and provide administrative support when necessary.
  • Provide administrative support to the CRA and COA during project close-out.

Desired Qualifications

  • Flexibility to perform multiple tasks and ability to prioritize them to achieve project timelines.
  • High commitment to consistently performing high-quality work.
  • Effective problem-solving skills.
  • Demonstrate a positive attitude, teamwork, proactiveness, and confidence.
  • Good learning ability.
  • Action-oriented approach.
  • Flexible attitude toward assignments and new learning.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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