Sponsor Dedicated Site Activation Specialist II - home based in Spain

Syneos Health, Inc.; Córdoba; A distancia; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a dedicated Site Activation Specialist to join their dynamic team. This role is crucial in ensuring quality deliverables and managing timelines for clinical trial processes. You will collaborate with a diverse group of professionals, driving innovation and excellence in site start-up activities. With a commitment to fostering a supportive and inclusive work environment, this organization values your contributions and offers opportunities for growth and development. If you are passionate about making a meaningful impact in the biopharmaceutical field, this is the perfect opportunity for you.

Servicios

Career Growth Opportunities

Supportive Management

Training and Recognition

Diverse and Inclusive Environment

Formación

• Understanding of clinical trial processes and ICH GCP guidelines.
• Experience with clinical trial start-up processes and managing vendors.

Responsabilidades

• Ensure quality deliverables and manage submission timelines.
• Monitor financial aspects and support continuous quality improvements.

Conocimientos

Organizational Skills

Communication Skills

Interpersonal Skills

Problem-Solving Skills

Attention to Quality

Educación

Bachelor’s Degree

Descripción del empleo

Sponsor Dedicated Site Activation Specialist II - home based in Spain

Updated : Yesterday

Location : Europe-Spain, Spain

Job ID : 25003101

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

Our Clinical Development model centers on the customer and the patient. We aim to simplify and streamline our work to make Syneos Health both easier to work with and for.

Whether joining us in a Functional Service Provider 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 therapy delivery because we are passionate about changing lives.

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

Why Syneos Health

• We develop our people through career growth, supportive management, training, recognition, and rewards.
• We foster a Total Self culture, where everyone can be authentic. We are committed to caring for our people.
• We strive to build a diverse and inclusive environment where everyone feels they belong.

Job Responsibilities

• Ensure quality deliverables at the country level, following project requirements and country regulations with oversight from the SSU Country Manager.
• Manage submission and approval timelines, track milestones, investigate delays, and escalate issues promptly.
• Monitor financial aspects and resource allocation, escalating discrepancies as needed.
• Adhere to SOPs and WI, keep training records updated, and ensure timesheet compliance.
• Support continuous quality improvements in Site Start-Up components at the country level.
• Ensure all documents are submitted to the Trial Master File as per SOPs and sponsor requirements.
• Perform functions such as Local Submissions Specialist, supporting regulatory submissions and site activation processes.
• Support country-level start-up activities, including regulatory intelligence, site feasibility, and contract negotiations.

Qualifications

• Bachelor’s Degree
• Understanding of clinical trial processes across Phases I-IV and ICH GCP guidelines.
• Ability to interpret clinical protocols and study specifications.
• Experience with clinical trial start-up processes.
• Ability to manage external vendors effectively.
• Strong organizational, communication, and interpersonal skills.
• Experience managing complex project budgets.
• Attention to quality and problem-solving skills.
• Relevant local (Spanish) experience is required.

Get to know Syneos Health

We have worked with 94% of FDA-approved drugs, 95% of EMA-approved products, and over 200 studies involving 73,000 sites and 675,000+ patients.

Join us to challenge the status quo in a dynamic environment. Learn more about us.

Additional Information :

Tasks and responsibilities are not exhaustive. The company may assign other duties at its discretion. Qualifications may be considered equivalent. This description does not create an employment contract. We comply with applicable legislation, including the EU Equality Directive and the Americans with Disabilities Act, providing accommodations as needed.

Work here matters everywhere. Our work improves patients’ lives worldwide, and a career with Syneos Health guarantees meaningful impact.

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