Site Activation Specialist I

Third-Party Job Posts; Buenos Aires; Presencial; ARS 1.200.000 - 1.600.000; Jornada completa

Descripción de la vacante

A leading biopharmaceutical organization is seeking a Site Activation Specialist in Buenos Aires, Argentina. The role involves managing the site identification process, ensuring compliance with regulations, and excellent negotiation and communication skills are essential. Candidates should have a Bachelor's degree and a minimum of 3 years of relevant experience. This position offers an opportunity to make a significant impact on the delivery of therapies and patient outcomes.

Formación

• Minimum of 3 years of experience in site start-up or site identification.
• Strong understanding of regulations and project requirements.
• Detail-oriented with strong organizational skills.

Responsabilidades

• Manage and execute the site identification process.
• Negotiate site confidentiality agreements with sites.
• Track completion of site identification documentation.

Conocimientos

Negotiation skills

Communication skills

Problem-solving skills

Organizational skills

Educación

Bachelor's degree in a relevant field

Herramientas

Relevant software tools

Descripción del empleo

Site Activation Specialist

ISyneos 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.

Responsibilities

• Manage and execute the site identification process in accordance with regulations, SOPs, and project requirements, ensuring timely and accurate completion of all tasks.
• Complete and negotiate site confidentiality agreements (CDAs) and site information forms (SIFs) with sites, ensuring compliance with legal and regulatory requirements.
• Maintain, review, and report on site performance metrics, identifying areas for improvement and implementing corrective actions as needed.
• Serve as the primary point of contact for investigative sites, providing support and guidance throughout the site identification process.
• Track the completion of site identification for sites, ensuring all necessary documentation is collected and maintained in accordance with SOPs and project requirements.
• Contribute to the design, implementation, and delivery of processes, programs, and policies, using knowledge and skills typically acquired through advanced education and experience.
• Utilize practical knowledge of the professional area to manage defined components of projects or processes within area of responsibility, ensuring alignment with overall project goals and objectives.
• Direct the work of lower‑level professionals or manage processes and programs, providing guidance and support to ensure successful completion of tasks.
• Collaborate with cross‑functional teams to ensure seamless integration of site identification activities with other project components.
• Stay current with industry trends and best practices, incorporating new knowledge and skills into daily work to enhance overall performance.

Qualifications

• Bachelor’s degree in a relevant field or equivalent experience.
• Minimum of 3 years of experience in site start‑up or site identification.
• Strong understanding of regulations, SOPs, and project requirements related to site identification.
• Excellent negotiation and communication skills.
• Ability to manage multiple tasks and projects simultaneously.
• Detail‑oriented with strong organizational skills.

Certifications

• Certification in clinical research or related field preferred.
• Training in Good Clinical Practice (GCP) and other relevant regulations.

Necessary Skills

• Proficiency in site confidentiality agreements (CDAs) and site information forms (SIFs).
• Ability to maintain, review, and report on site performance metrics.
• Strong problem‑solving and analytical skills.
• Effective communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency in relevant software and tools.

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 qualificat