Key Facts

Remote From:

Full time

Mid-level (2-5 years)

English

Hard Skills

MedDRA WHO Drug Dictionary (WHO-DD) Clinical Data Management Medical Coding Cross-Functional Collaboration Accident Reporting Clinical Data Management Standard Operating Procedure Pharmacovigilance Regulatory Compliance Medical Coding Clinical Trial Planning Pre-Clinical Development Online Communication Positive Discipline

Other Skills

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Non-Verbal Communication
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Analytical Skills
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Multitasking
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Time Management
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Teamwork
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Organizational Skills
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Detail Oriented
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Problem Solving

Roles & Responsibilities

Bachelor’s degree in Nursing, Biology or related scientific fields.
At least 2 years of experience in a clinical coding role.
Firm knowledge of clinical data coding methodologies and familiarity with global regulatory and data management standards (e.g., ICH GCP, safety reporting).
Proficiency with major coding dictionaries (e.g., MedDRA, WHODrug) and strong written/verbal communication skills.

Requirements:

Code assigned clinical trials.
Review coded data for consistency, accuracy, and compliance with coding guidelines.
Prepare and forward coding reports for medical review.
Collaborate with cross-functional teams to ensure timely, accurate coding aligned with project goals and regulatory requirements.

Parexel

Pharmaceuticals

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 With HeartTM 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.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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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.

Parexel is currently seeking a Clinical Coder to join us in South Africa or Poland, dedicated to a single sponsor. This will be home-based position.

This role will be responsible for performing medical coding activities for clinical studies, providing support to various departments (e.g. Clinical Development, Pharmacovigilance) as needed, and contributing to the development and implementation of departmental medical coding Standard Operating Procedures (SOPs) and work practices.

Previous experience in a similar role is essential.

Working as a Clinical Coder at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

Expect exciting professional challenges in inspiring studies, but with time for your outside life.

Base Pay Range for Poland: PLN 141,500 to 199,100.

Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location.

In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance-based bonus plan, annual salary review and total rewards incentives.

Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles.

Responsibilities

Responsible for coding assigned clinical trials.
Coding medical review - Responsible for review of coded data for coding consistency, accuracy, and compliance with coding guidelines.
Prepares and forwards coding reports for medical review.
Collaborates effectively with cross-functional teams to ensure accurate, consistent, and timely medical coding that aligns with project goals and regulatory requirements.

Here are a few requirements specific to this advertised role.

Bachelor’s degree in Nursing, Biology or related scientific fields.
At least 2 years of experience in a clinical coding role.
Firm knowledge and understanding of clinical data coding methodologies as well as current and emerging global regulatory and data management standards.
Good knowledge of research and development, clinical trials execution, and understanding of regulatory requirements/guidelines (e.g. ICH GCP, safety reporting).
Sound knowledge of major coding dictionaries (e.g. MedDRA, WHODrug).
Strong written and verbal communication skills.
Ability to interpret and apply coding guidelines.
Must be disciplined, detail-oriented, and able to multitask and work efficiently and independently.
Excellent time management and organizational skills.
Ability to work in a team environment.
Highly developed problem-solving and analytical skills.

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

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