Description

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  

Every day we perform better because of how we work together, as one team, each the best at what we do. We bring a wide range of talented experts together across a wide range of business-critical services that support our business. Every role within Corporate is vital to furthering our vision of Shortening the Distance from Lab to Life®.

Discover what our 29,000 employees, across 110 countries already know: 
WORK HERE MATTERS EVERYWHERE

Why Syneos Health
•    We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
•    We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. 
•    We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Syneos Health is looking for a detail-oriented regulatory lawyer to join its Legal team. The successful candidate will be a self-starter with a solution-oriented approach, excellent judgment and the ability and desire to learn new things.

Job responsibilities

Provides legal regulatory advice and counsel on global regulatory and clinical development matters; Provides legal and regulatory advice to Corporate Quality and the clinical business on quality-related issues, regulatory authority inspections, client and internal audits; Provides legal support on litigation and pre-litigation matters as appropriate; Advises internal teams on the application of medicinal product and medical device laws and regulations as well as GxP as they relate to clinical research; Provides legal support for communications with regulatory authorities; Provides legal support for compliance and quality investigations as appropriate; Keeps abreast of legislative and regulatory changes that may affect the company and its clients; Advises on regulatory and Quality Assurance commitments in clinical and commercial agreements. Works collaboratively across the Legal department, including the Company’s global team of regional-based lawyers, in providing legal regulatory advice, building consensus on process improvements, and driving corporate legal projects to completion.

Qualifications

Qualifications

Fully qualified lawyer with 3+ years of post-qualification experience; Experience advising on legal and regulatory matters in the pharmaceutical / healthcare industry is a strong plus; Ability to communicate clearly, concisely, and professionally with all levels of management; Ability to work independently while being able to contribute successfully to cross-functional teams; Independent judgment, attention to detail, and desire to learn; Ability to prioritize tasks to meet tight deadlines in a fast-paced environment; Can-do attitude, ability to work under pressure and to manage client expectations; English C2- full professional proficiency