Safety Physician

Medpace; London; On-site; GBP 80,000 - 120,000; Full time

Job summary

A leading clinical research organization is seeking Clinical Safety Physicians to enhance its pharmacovigilance team. The role involves medical review of adverse events, collaboration across departments, and ensuring compliance with safety regulations, offering great opportunities for career growth. The position can be based in the UK or flexible home-based depending on experience.

Benefits

Competitive salary

Benefits package

Qualifications

• At least 4 years of clinical research experience, preferably in Pharmacovigilance/Safety Surveillance.

Responsibilities

• Review individual adverse event reports and aggregate safety data.
• Collaborate with Medical Monitors and ensure regulatory compliance.
• Provide oversight for safety documents and clinical study protocols.

Skills

Strong communication skills

Interpersonal skills

Ability to work collaboratively

Education

MD Degree or equivalent

Medical licensure

Job description

Our operational activities are growing rapidly, and we are currently seeking Clinical Safety Physicians to join our team. This position plays a key role in the pharmacovigilance process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.This position can be based in one of our European offices, or home based (subject to level of experience). We offer a Competitive salary and benefits package.

Responsibilities

• Medically review individual adverse event reports with assigned studies, both clinical trials and post-marketing;
• Review of aggregate safety data during conduct of study for any safety signals
• Collaborate with Medical Monitors, Clinical Safety, and Biometrics ;
• Provide oversight and key input for review of new or on-going safety documents, such as DSUR;
• Provide safety review of clinical study documents, including protocols, study reports; and marketing application components;
• Collaborate with other departments to ensure appropriate collection and handling of safety data; and
• Ensure regulatory compliance and safety throughout trial.

Qualifications

• MD Degree or equivalent;
• Medical licensure;
• At least 4 years of clinical research experience, preferably in Pharmacovigilance/Safety Surveillance;
• Strong communication skills (both written and oral) and strong interpersonal skills; and
• Ability to work collaboratively as part of a team.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Awards:

• Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
• Recognized by Forbes as one of America's Best Mid-size Companies in 2021
• Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

EO/AA Employer M/F/Disability/Vets

*WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.

About the company

Medpace Holdings, Inc. is a midsize, clinical contract research organization based in Cincinnati, Ohio.

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