Parexel

MLR Vault Technician

Parexel  •  Hyderabad, IN (Remote)  •  4 hours ago
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Job Description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

The MLR Technical Reviewer will be responsible for completion of tasks in the MLR Platform of Veeva Vault PromoMats and Veeva Vault Medical, the tasks will be related to the role of Content Administrator, i.e. Creating Placeholders, Uploading versions, Reference Linking, Anchoring & Linking, monitoring the Workflows/Task completion.


The MLR Technical Reviewer will work in an international and cross-functional environment, following global and local guidelines and working closely with internal and external stakeholders to ensure the highest quality for assets and gathering data on asset quality and agency performance.

  • Create new placeholders, based on relevant Metadata & guidance provided
  • Uploading new MLR content, based on relevant Metadata & guidance provided
  • Uploading new Reference Documents and sending them for QC, based on relevant information & guidance provided
  • Reference Document linking, based on relevant information & guidance provided
  • Anchoring & Linking, based on relevant information & guidance provided
  • Starting QC workflows, based on relevant information & guidance provided
  • Monitoring MLR workflows, based on relevant information & guidance provided
  • Communicating with users or stakeholders to inform about task progress or completion

Skills:

  • Relevant Scientific, Medical or Data Analysis background preferred
  • Relevant experience with Veeva Vault PromoMats or Medcomms preferred
  • Strong attention to detail and accuracy, ability to manage and prioritize multiple, detailed activities, results-orientated with fast and focused execution.
  • Good communication, coordination and time management skills.
  • Fluent in oral and written English
  • Ability to work within a team or across multiple teams (including remotely) as well as independently.
  • Values teamwork and collaboration, diversity and inclusion, and innovation.
  • Prior experience working in content creation for Biotech/Pharma, would be advantageous.
  • Prior experience with the Pharmaceutical Content Review process and/or Veeva Vault would be advantageous.
Parexel

About Parexel

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines

Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.

• Defamatory, offensive, obscene, vulgar or depicting violence.

• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,

sexual preference or orientation, nationality or political beliefs.

• Sexually explicit or pornographic.

• Fraudulent, deceptive, libelous, misleading or unlawful.

• Referencing criminal or illegal activity.

• Spamming.

We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Raleigh, North Carolina
Year Founded
Unknown
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