Key Facts

Remote From:

India

Full time

Mid-level (2-5 years)

English

Hard Skills

Clinical Trials SAS (Software) Stakeholder Communications Project Management Process Improvement Pharmacokinetic Dosing

Other Skills

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Professionalism
•
Analytical Skills
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Teamwork
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Detail Oriented
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Verbal Communication Skills

Roles & Responsibilities

PhD in Statistics or related discipline (or MS in Statistics or related discipline with some experience)
Prior experience with SAS programming (desirable)
Knowledge of pharmacokinetic data is an advantage
Ability to work independently and strong mentoring/leadership skills

Requirements:

Production and/or QC of derived datasets and statistical outputs using efficient programming techniques
Understand and apply moderately advanced statistical methods
Coordinate and lead a project team to successful completion within given timelines and budget; interact with clients as key contact regarding statistical and contractual issues
Check own work in an ongoing manner to ensure first-time quality; provide training in statistical analysis to internal clients

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.

Key Accountabilities:

Operational Execution

Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniques
Understand and apply moderately advanced statistical methods
Coordinate and lead a project team to successful completion of a project within given timelines and budget
Interact with clients as key contact with regard to statistical and contractual issues
Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents
Check own work in an ongoing manner to ensure first-time quality
Provide training in statistical analysis to internal clients
Proactively participate in and/or lead process/quality improvement initiatives
Travel to, attend and actively contribute to all kind of client meetings as appropriate (eg discussing analysis concepts, presenting and discussing study results

General Activities

Mentor and train junior members of the department
Additional responsibilities as defined by supervisor/manager

Business Development

Support of Business Development, eg by attending and preparing bid defense meetings

Skills:

Good analytical skills
Good project management skills
Professional attitude
Attention to detail
A good understanding of statistical issues in clinical trials
Prior experience with SAS programming desirable
Ability to work independently
Good mentoring/leadership skills

Knowledge and Experience:

PhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experience
The knowledge of pharmacokinetic data is an advantage
Competent in written and oral English in addition to local language

Education: