Clinical Operation Specialist Assigned to Client Hybrid Mexico

**Description**

Clinical Operation Specialist assigned to client Hybrid Mexico

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**

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.

**Responsibilities**:

- Reviewing study protocols and executing procedures in alignment with protocols and regulatory, health, and safety standards, ensuring compliance with all relevant guidelines and regulations
- Recruiting and coordinating communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study
- Following applicable regulations globally and by region, ensuring that all activities are conducted in accordance with local and international standards
- Collaborating with cross-functional teams to develop study materials, including informed consent forms, study manuals, and other essential documents
- Monitoring trial progress and addressing any issues that arise during the study, ensuring that all problems are promptly identified and resolved
- Providing organizational related support or service, typically under supervision, assisting with administrative tasks and other support activities as needed
- Performing routine tasks with some deviation from standard practice, adapting to changing circumstances and requirements as necessary

**Qualifications**
- High school diploma or equivalent required
- Associate's degree or higher in a related field preferred
- Minimum of 2 years of experience in clinical operations or a related field
- Strong understanding of clinical research protocols and regulatory requirements

**Certifications**
- Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred
- Basic Life Support (BLS) certification required

**Necessary Skills**
- Excellent communication and interpersonal skills
- Strong organizational and time management abilities
- Attention to detail and accuracy in documentation
- Ability to work effectively in a team environment
- Proficiency in Microsoft Office Suite and clinical trial management software

**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. Learn more about Syneos Health.

**Additional Information**

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with