Clinical Trial Manager​/Local Study Manager

Clinical Trial Manager / Local Study Manager

Updated: Yesterday
Location: DEU-Remote
Job :

Description Clinical Trial Manager / Local Study Manager

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.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full‑Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

• 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.

Job Responsibilities

For one of our sponsors we are looking for a Clinical Trial Manager to join the team in Germany. This Local Study Manager is accountable for the strategic planning & management and performance of the assigned clinical trials from country allocation within the feasibility process until study closure. This includes study timelines, study budget, and study conduct in accordance with the sponsor’s SOPs and ICH/GCP and regulatory guidelines & directives.

The role is responsible for identifying and anticipating risks jeopardizing trial performance and developing and initiating countermeasures based on proposed planning and regular revision of the plans. It acts at the country level as the key strategic interface with internal and external stakeholders to develop, implement, maintain, and improve operational processes to accelerate trial conduct in close collaboration with different functions and other departments, e.g. Medical Advisor, Site Engagement Manager, Strategic Start‑Up Manager, Medical Science Liaisons.

The role acts as person of contact within a therapeutic area in terms of study management and conduct and leads a study team through change‑management efforts and by example.

Qualifications

• Bachelor’s degree or higher degree in Health or Natural Sciences
• Three years of experience in clinical research
• Experience in project management and prior time as field monitor or site coordinator
• International experience preferred
• Fluency in German and English
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Excellent communication, presentation and interpersonal skills

This posting is intended for a possible upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.

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Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, please contact us at: