Updated: Yesterday  Location: POL-Warsaw-Hybrid  Job ID: 25101667

Overview

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 centers on the customer and the patient, and we aim to simplify and streamline our work to be easier to work with for our teams and clients. We operate in Functional Service Provider partnerships or Full-Service environments and collaborate with problem solvers to accelerate the delivery of therapies that change lives.

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people through career development and progression; supportive line management; technical and therapeutic area training; peer recognition and total rewards program.
• We embrace our Total Self culture, uniting us globally and taking care of our people.
• We value diversity of thoughts, backgrounds, cultures, and perspectives to create a sense of belonging for all.

Job Responsibilities

• Develop, coordinate, and implement Phase 1 clinical research studies at the organization-s facilities, ensuring adherence to study protocols and timelines.
• Collaborate with the principal investigator to design study protocols and ensure scientific integrity.
• Liaise between research subjects, client teams, investigators, and clinic operations teams to facilitate smooth communication and coordination.
• Plan logistics and resource usage for clinical trials, including scheduling, staffing, and equipment needs.
• Track study progress in alignment with project milestones, client deliverables, and budget; provide regular updates to stakeholders.
• Ensure compliance with applicable regulations globally and by region, including Good Clinical Practice (GCP) guidelines.
• Supervise experienced support employees and/or entry-level individual contributors, planning, prioritizing, and directing their tasks to ensure efficient workflow and high-quality output.
• Deliver operational results with a moderate impact on the immediate achievement of team results and contribute to organizational success.
• Adapt new procedures, techniques, and tools to improve clinical trial processes and outcomes.
• Understand basic management approaches such as work scheduling, prioritizing, coaching, and process execution.

Qualifications

• Broad job knowledge in an operational, administrative, and/or specialized field.
• Practical knowledge in managing the execution of processes, projects, and tactics within a team.
• Understanding of the impact of work on related areas.

Certifications

• Relevant certifications in clinical trial management or related fields

Necessary Skills

• Strong leadership and management skills
• Excellent communication and collaboration abilities
• Ability to plan and prioritize tasks effectively
• Proficiency in tracking and reporting study progress
• Knowledge of global and regional regulations for clinical trials

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 studies across 73,000 sites and 675,000+ trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.

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. If you require a reasonable accommodation to complete any part of the application process, please contact us at jobs@syneoshealth.com.

Summary

Roles within the Clinical Trial Management job family at the M23 level are responsible for overseeing the development, coordination, and implementation of Phase 1 clinical research studies at the organization-s facilities. These roles involve collaboration with the principal investigator, liaisons between research subjects, client teams, investigators, and clinic operations teams, and planning logistics and resource usage. Individuals in these roles track study progress in alignment with project milestones, client deliverables, and budget, while ensuring compliance with applicable regulations globally and by region. They contribute to the advancement of medical knowledge and the development of new treatments through effective resource management and coordination.