Skip to main content

This job has expired

Senior Medical Director - Cell & Gene Therapy

Employer
Parexel
Location
United Kingdom
Salary
Competitive
Start date
25 Feb 2021
Closing date
27 Mar 2021

View more

Discipline
Medical Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Job Description

During the last five years, Parexel has participated in more than 1,000 oncology and hematology clinical projects. The range of services includes compound clinical development planning, collaboration with feasibility, protocol writing or optimization, medical monitoring and pharmacovigilance. Parexel has global presence in every phase of clinical research and expertise in virtually every indication and mechanism of action, including novel immuno-oncology agents, cellular based therapy, and cell and gene therapy. Join our growing team of oncologists/hematologists and make a difference in the lives of patients searching for more effective and better tolerated cancer therapies.

We are currently seeking Board Certified physicians to join Parexel as Medical Directors with a focus on cell and gene therapies.

As a Medical Director at Parexel focusing on cell and gene therapy, 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:

•Meet with clients for early engagement and strategy discussion including industry and investigator meetings.
•Help coordinate training and standard operating procedures for cell and gene therapy trials.
•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 meetings ie. Investigator Meetings.Qualifications

Successful applicants will be Board certified with clinical trial experience.Training for this role may include hematology and oncology, neurology, cardiovascular disease, infectious diseases, neurology, or others to be considered.Experience in industry is a plus.Trained in cellular therapies, including but not limited to, CAR-T cells and be familiar with the fundamentals of gene therapy trials.

- 25% travel is requiredWhy Work at Parexel

There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

That's Parexel. We're a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.

How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.

Company

Parexel International Corporation is a leading global biopharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, Parexel has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Parexel Informatics, Inc., a subsidiary of Parexel, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process.

 

Mission: Parexel’s mission is to combine the strength of our expertise, experience and innovation to advance the worldwide success of the bio/pharmaceutical and medical device industries in preventing and curing disease.

 

Company info
Website
Telephone
+44 1895 238000
Location
The Quays
101-105 Oxford Road
Uxbridge
Middx
UB8 1LZ
GB

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert