Executive Medical Advisor - UK - Remote

Executive Medical Advisor - UK - Remote

Executive Medical Advisor - UK - Remote

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

What Medical Affairs does at Worldwide

Medical Affairs plays a pivotal role throughout the entire life cycle of a clinical investigation, exerting its influence from the initial stages of Business Development to the final Regulatory Submissions. Within this multifaceted domain, the dedicated members of the Medical Affairs team provide essential support to the broader project team, contributing to the cultivation of the scientific and medical principles that define Worldwide's philosophy.

What you will do

• Represents the medical and scientific expertise within the Company and provides therapeutic and protocol specific insight for clinical research programs.
• Maintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances by review of relevant therapeutic/clinical literature and attendance in conferences and meetings.
• Interacts with staff in other functional areas to ensure the highest level of client satisfaction through successful execution of projects.
• Responsible for selected project data review and analysis.
• Identifies, documents and appropriately resolves out-of-scope work as directed by senior management.
• Maintains working knowledge of GCPs and regulatory requirements relating to clinical development and safety; assures compliance with ethical, legal and regulatory standards.
• Mentors other medical staff as directed by Senior management and by consistently displaying exemplary work ethics, compassion and integrity, supports Senior Management’s leadership of both the department and the company.
• Maintains clinical/therapeutic acumen in medical subspecialty through online and/or in person scholarly programs/lectures.

What you will bring to the role

• Excellent written and verbal communication skills to clearly and concisely present information.
• Strong planning, strategizing, managing, monitoring, scheduling, and critiquing skills.
• Strong interpersonal skills in a collaborative work environment.
• Excellent ability to handle multiple tasks in a fast-paced and constantly changing environment.
• Ability to exercise sound judgment and make decisions independently.
• Excellent self-motivation skills; proactivity. Proficiency in all MS-Office applications including Microsoft Word, Excel, and PowerPoint.
• Knowledge of study design and statistical analyses as they apply to controlled clinical trials.

Your experience

• Medical degree with 10 or more years of experience in clinical research and drug development.
• Demonstrable knowledge of therapeutic expertise, with a track record in drug development.
• Demonstrable knowledge of operational aspects Phase I-IV clinical research.
• Demonstrated ability to establish and maintain highly effective relationships with sponsors and external vendors.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide.