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PAREXEL International LLC Senior Consultant, Clinical Outcomes Assessment in United States

Senior Consultant, Clinical Outcomes AssessmentUSA - Any Region - Home BasedDate posted11/20/2020Job ID64197BR

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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.

  • Full Time

  • Level: Mid

  • Travel: Yes

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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.


Parexel Access Consulting (PAC) provide consultancy services to help clients prepare for market access throughout the drug development lifecycle. Our experts work closely with clients to build robust strategies to showcase a product’s value, help support payer and HTA acceptance, and ultimately help gain optimal reimbursement and market access for their product. We have experts in health economic modeling, pricing and market access, real-world data, evidence evaluation and clinical outcome assessment.

As a Senior Consultant/Associate Director, Clinical Outcomes Assessment you will oversee and consult on a range of projects in the field of COAs. This is an exciting opportunity to lead and build on our growing COA consultancy team in the US. Duties will be varied, but will be broadly split between research, consultancy, project management and business development. In this role you will work with colleagues and clients both locally and globally, on a variety of studies across multiple therapeutic areas.

Research and consultancy tasks will include:

•Participation in strategic meetings

•Designing studies

•Preparing study protocols

•Conducting literature reviews

•Recruiting participants, qualitative interviewing and analysis and developing questionnaires/surveys.

•You will be responsible for small and medium sized projects, including managing budgets and timelines and acting as a day-to-day client contact.

•Business development activities may include the preparation of proposals and presentations to clients.

•There will also be opportunities to contribute to thought leadership activities, including conference abstracts, peer-reviewed publications and white papers.


Ideal candidate will possess:

•A minimum of a Master’s degree in psychology, epidemiology, public health, outcomes research, health sciences or related area; PhD strongly preferred.

•Several years of experience in running qualitative or quantitative research projects in a related field (e.g. protocol development, study design, data collection, analysis, writing reports)

• 8-10 years of demonstrable experience in COA research (development/strategy)

•Experience applying COA expertise within the industry (CRO experience preferred)

•Familiarity with guidance on the use of COAs in drug development and market access

•Experience in qualitative research (e.g. interviews, focus groups, NVivo)

•Experience in conducting literature/instrument reviews

•Project management experience including handling deadlines, changes in scope and budget

•Ability to work independently and as part of a team in a fast-paced commercial environment with a sense of urgency

•Excellent oral and written communication skills

EEO DisclaimerParexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.