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Parexel Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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 ...

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Parexel information

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$33K

$71.9K

$116.5K

How much do parexel jobs pay per year?

As of Aug 3, 2026, the average yearly pay for parexel in the United States is $71,948.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $85,000.00 per year, depending on experience, location, and employer.

What does Parexel Company do?

Parexel is a global biopharmaceutical services organization that provides clinical research, regulatory consulting, and commercialization services to pharmaceutical, biotech, and medical device companies. The company employs professionals such as clinical research associates and regulatory specialists to support drug development and approval processes. It operates in a regulated environment requiring compliance with industry standards and often involves project management and data analysis skills.

What are the main responsibilities of a Clinical Research Associate (CRA) at Parexel, and how does the role contribute to clinical trial success?

As a Clinical Research Associate (CRA) at Parexel, you will oversee the progress of clinical trials at investigational sites to ensure they are conducted, recorded, and reported in accordance with protocol, Good Clinical Practice (GCP), and regulatory requirements. This involves frequent site visits, monitoring data integrity, and maintaining close collaboration with site staff and clinical project teams. CRAs play a pivotal role in identifying and resolving issues early, supporting patient safety, and ensuring trial milestones are met. The role requires strong communication skills, attention to detail, and the ability to work both independently and as part of a global team.

What are the key skills and qualifications needed to thrive at Parexel, a leading clinical research organization, and why are they important?

To thrive at Parexel, you generally need expertise in clinical research, regulatory compliance, and data analysis, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as GCP (Good Clinical Practice) are commonly required. Strong attention to detail, teamwork, and effective communication are standout soft skills in this environment. These abilities ensure the accuracy, compliance, and collaborative spirit needed to deliver high-quality research outcomes for clients and regulatory agencies.

How much does Parexel pay?

Salaries for roles at Parexel vary depending on the position, experience, and location. Entry-level positions typically start around $60,000 annually, while more experienced roles can pay over $100,000. Compensation often includes benefits such as health insurance and performance bonuses.

What is Parexel and what does the company do?

Parexel is a global clinical research organization (CRO) that provides a range of services to the biopharmaceutical and medical device industries. The company specializes in conducting clinical trials, regulatory consulting, and providing technology solutions to help bring new medical treatments to market. Parexel partners with pharmaceutical, biotechnology, and medical device companies to support drug development from early-phase research through to post-marketing surveillance. Their services help ensure that new therapies are safe, effective, and compliant with regulatory standards.

How do I get into Parexel?

To get into a role at Parexel, candidates should review current job openings on the company's careers page, ensure they meet the required qualifications and experience, and submit an application online. Preparing a tailored resume and cover letter highlighting relevant skills, such as clinical research knowledge or regulatory understanding, can improve chances. Networking and obtaining relevant certifications, like GCP or clinical trial training, may also be beneficial.

Is Parexel a good place to Work?

Parexel is a global biopharmaceutical services company that offers roles in clinical research, regulatory consulting, and data management. Employees often cite a collaborative environment, opportunities for professional development, and competitive benefits, though experiences can vary by location and role.
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Infographic showing various Parexel job openings in the United States as of July 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 55% Physical, and 45% Remote job distribution, with an average salary of $71,948 per year, or $34.6 per hour.

Medical Director, Endocrinology

Parexel

Remote

Full-time

Posted 14 days ago


Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

29th of 72 rated research


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.
Parexel's endocrinology team brings deep expertise across the full clinical spectrum-from rare metabolic disorders to programs in obesity and diabetes.
We currently have an exciting opportunity available for an Associate/Medical Director/Senior Medical Director, Endocrinology to join our exceptionally talented and patient focused General Medicine team.
Key Accountabilities
As a Medical Director, you will provide medical monitoring for assigned projects, function as medical representative on the project team, provide medical consultation as required or requested to client/sponsor or to other Parexel service groups, and assume the role of Senior Technical Lead in selected circumstances.
In addition, you will also:
  • Review all individual adverse experience reports for accuracy and clinical importance, and characterize their relationship to the study drug, severity and seriousness.
  • Provide reports to FDA or other regulatory agencies and the sponsor on a periodic and regular basis, summarizing adverse experiences as required by FDA or the sponsor, depending on the contract.
  • Review data listings of safety data, including adverse experiences, laboratory data, and vital signs data, to establish the presence or absence of abnormal trends, and if noted, follow up as appropriate with the project team, sponsor, investigator, and FDA.
  • Review documents written by various Parexel divisions for safety issues.
  • Review coding of adverse events and concomitant medications for accuracy and consistency.
  • Provide support for the preparation of clinical protocols, integrated clinical and statistical summary reports, journal articles, and other documents for clients/sponsors or in conjunction with clients/sponsors and in conjunction with other Parexel divisions.
  • Attend and present material, as requested, at meetings within Parexel as well as extra-company external meetings and conferences.

Education, Skills, Knowledge and Experience:
Successful applicants will:
  • be a MD Endocrinologist (or equivalent international credential)
  • have extensive clinical experience treating adult patients with Obesity, MASH/NASH, and Diabetes is highly preferred.

Past experience as a Physician in Industry or as a Clinical Trial Primary Investigator or Sub-Investigator is highly preferred; however, consideration will be given to exceptional candidates with an interest in transitioning to Industry. (Candidate experience will determine Associate Medical Director, Medical Director or a Senior Medical Director role).
Successful applicants will also have:
  • Excellent interpersonal skills including the ability to interact well with sponsor/client counterparts.
  • Excellent time management skills
  • Excellent verbal and written medical communication skills.
  • Excellent standard of written and spoken English
  • A flexible attitude with respect to work assignments and new learning
  • The ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
  • A willingness to work in a matrix environment and to value the importance of teamwork.
  • The ability to travel up to 20% domestically and/or internationally as needed.

#LI-SM1
EEO Disclaimer
Parexel 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.

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PAREXEL logo

About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983