(Senior) Medical Director, Gastrointestinal

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 in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.

Parexel is looking for a Medical Director/Senior Medical Director with a strong background in Gastroenterology.

Must have completed Gastroenterology specialty training and have clinical experience in this area.

The role can be based remotely in the UK or select EMEA locations.

The Medical Director is a medical expert with specialized therapeutic expertise and some experience across indications, clients and drug development. They initiate and maintain medical and consultative relationships with clients, consult on early engagement and pre-award efforts and serve as a medical monitor for contracted projects. The Medical Director may take on leadership roles by participating in initiatives, mentoring junior MDs and/or, where appropriate, managing a team of physicians.

KEY ACCOUNTABILITIES:

Project Execution: Medical Monitoring Delivery & PV Support

• Independently deliver all medical support required for successful delivery of the projects according to contracted agreement with the sponsor (i.e., tasks and time per task contracted) and according to the assigned role (Global Lead Physician or Regional Lead Physician)

• Participate actively in study planning with feasibility leaders, solution consultants

• Participate in team project and investigator meetings

• Provide training of study teams on TA indication and protocol (Note that this does not include any direct medical advice on patient care or management)

• Communicate with relevant sponsor counterparts on challenges and accomplishments related to assigned project/study

• Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical and statistical summary reports, safety plans, Informed Consent Forms, etc. in conjunction with clients/sponsors or in conjunction with other Parexel departments

• Deliver medical monitoring activities according to MMP during the study conduct

• Deliver medical leadership to the project in close coordination with the Project Leader and according to the role assigned either GLP or RLP

• Provide medical input into PV workflows and projects and participate in safety processing for studies including medical review of serious adverse events

Client Relationship Building & Engagement

Support Business Development

Provide medical expertise to client across multiple channels and interactions

• Consultancy on protocol development or drug development program

• Medical review of various documents, which might be audited by clients and regulatory agencies

• Provide medical expertise and training to other Parexel colleagues​
  ​

KNOWLEDGE & EXPERIENCE:

• Must have completed gastroenterology specialty training to be considered for the role.

• Clinical and/or research experience in MASH (metabolic associated liver disease) and/or IBD (Crohn's disease and ulcerative colitis)

• A background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design/execution preferred.

• Clinical practice experience

• Good knowledge of the drug development process including drug safety, preferred

• Experience in Pharmaceutical Medicine, preferred

• Experience leading, mentoring and managing individuals/ a team, preferred

• Excellent English language skills