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Senior Associate Real World Evidence

Sweden - Any Region - Home Based Date posted 05/16/2022 Job ID 81348BR

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.

In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.

Success Profile

Check out the top traits we're looking for and see if you have the right mix.

  • Detail-Oriented
  • Proactive
  • Problem-Solver
  • Results-Driven
  • Organized
  • Multi-Tasker
  • "When submitting major market applications, it’s key to ensure that the technical integrity of all data meets regulated requirement standards. Parexel makes this possible with a diverse team of seasoned professionals who care about getting important medicines to patients. This is Regulatory Operations at its best."

    Chris – Associate Director, Regulatory & Access
  • "In this role, I have had the unique opportunity to work with regulatory experts who are not only some of the most distinguished in their field, but are also some of the most compassionate people I know. I’ve been able to grow so much professionally by standing on the shoulders of giants!"

    Riley – Regulatory Affairs Consultant


  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Management

    Strong management with depth of experience working for global health authorities.


We are looking for Senior Associate Real World Evidence to join our team in Sweden! As a Senior Associate RWE you will have technical knowledge and be keen to continually developing the skills as defined in the responsibilities section of this document. Working closely with a project lead and technical SMEs, you will take responsibility for ensuring that client work is performed, and delivered on time, meeting the quality expectations of Parexel Regulatory and Access and the client.

Key Accountabilities:

• Works effectively within a team environment but may work independently delivering services within their area of competence. For a Senior Associate in RWE this would include tasks such:
  • Development of RWE client ready deliverables such as study protocols, data management and statistical analysis plans, data analyses, and study reports.
  • Development of analyses in programs such as SAS and R.
• Works within broad project guidelines as directed by the project lead/ manager and/or technical SMEs.
• Applies information provided by the project lead/manager or senior colleagues to complete assigned project activities.
• May support the project lead with project management activities.
Consulting Activities and Relationship Management
• Follows and implements the organization’s consulting models and methodologies under the guidance of the project lead and/or technical SMEs.
• Delivers consulting services within dedicated area of expertise under the guidance of the project lead and technical SME.
• Completes assigned activities within project scope and objectives with an understanding of issues which may impact project profitability under the direction of the project lead/manager.
• Identifies project and/or client needs to the project lead/manager and collaborates with senior staff to define a proposed solution.
• Identifies and alerts PC management to opportunities for follow-on business or necessary changes in project scope.
• Continue networking within the industry (i.e. maintain contacts and relationships with clients/data vendors once engagements are complete)


Knowledge and Experience required for the role:
• Minimum of a Master’s Degree in a Scientific or Technical Discipline
• Few years’ experience in an industry-related or consulting environment
• Good knowledge of SAS and R
• Keen interest in medical research, provision of healthcare and the pharmaceutical industry.
• Excellent interpersonal, verbal, and written communication skills - especially in the relaying of technical information.
• A high degree of written accuracy and attention to detail.
• High analytical ability.
• Client focused approach to work
• Self-motivation, enthusiasm, ambition and flexibility.
• Self starter, with the ability to takes responsibility for assigned work with moderate direction/support.
• Engages in two way dialogue and shares information with others on projects and initiatives. Participates in training initiatives under the guidance of their Development Manager.
• Fluent English, Swedish language skills would be a plus

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