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 FSP are currently recruiting for an experienced Clinical Development Feasibility Expert in Germany. This is a 100% remote position and is dedicated to one of our key global sponsors.
In this position you will be an invaluable resource working within the global clinical development and feasibility functions, you’ll support the teams with a quantitative, evidence and data driven approach, ensuring compelling narratives are developed. You will enhance strategies and execution through descriptive and predictive analytics, working with both internal and external data scientists. You’ll also support the development and integration of new tools including artificial intelligence and big data, to support trial scenario decision making.
Some specifics about this advertised role
100% homebased position
- Review of Evidence Plans, Trial Design Outlines and Clinical Trial Protocols.
- Review and analysis of information in internal- and external data bases.
- Presentation of charts and analysis of benchmark data.
- Establishing, Analysis and Consolidation of Metrics and Quality Review regarding Trial-, Country- and Site Lists.
- Running of scenario simulations, critical reviews, checks and provisions of results in the form of presentations (PPT).
- Alignment of findings with team members.
- Establish PPT Presentations, Reports and Communication based on templates and examples.
- Presenting in meetings.
- Preparation, Attention, Contribution, Minutes, Follow-Up in CDPH internal/external meetings.
- Project Management of upcoming tasks.
- Proactive communication to CDPH team members, trial- and program teams.
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.
What we are looking for in the this role
For every role, we look for professionals who have the determination and courage always to put patient well-being first.
That to us is working with heart.
Here are a few requirements specific to this advertised role.
- Prior Experience – successful work in a sponsor’s or CRO’s strategic feasibility team (planning of programs- and trial scenarios); understanding of country- and site feasibility.
- Clinical Development Knowledge – trial structures and dynamics (Regulatory Timelines, Site Initiation Curves, Screening Rate and Failure, Enrollment Rates and –Curves, Retention/Drop-Outs), understanding of Clinical Trial Protocols and Trial Designs.
- Data Analysis & Modeling – descriptive (e.g. box-whiskers charts, trend analysis, percentiles), predictive (Confidence Interval, Probability Densities and Curves).
- Abstract & Mathematical Thinking – translation of medical assumptions in quantitative analysis and statistics, understanding of limits and opportunities of models and data.
- Benchmarking & Scenario Planning – internal/external comparisons, identification of trends, descriptive statistics.
- Quantitative Forecasting – country-, site-, patient-number estimations, enrollment rates, timelines.
- Tool proficiency – advanced and expert MS Office knowledge, Especially Expert Excel knowledge.
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Top Skills
What We Do
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.
