Clinical Project Specialist (ideal opportunity for CTAs)hybrid BA Argentina

Clinical Project Specialist (ideal opportunity for CTAs) BA, Argentina Hybrid

Clinical Project Specialist (ideal opportunity for CTAs) BA, Argentina Hybrid.

Job Responsibilities

Project Management

• Uses performance metrics and quality indicators to assist the Global Trial Lead (GTL) in driving study execution.
• Resolves routine problems and escalates important issues appropriately (with a sense of urgency).
• Actively contributes as a key functional member on cross‑functional teams.

Study/Project Planning, Conduct and Management

• Understands study level tools and plans.
• Manages the development and/or collection of study level documentation and supports GTL in ensuring eTMF accuracy and completion for all studies.
• Provides and supports input to study level tools and plans while working with moderate to minimal supervision, including but not limited to the Transfer of Obligations to regulatory authorities, Study SharePoint/study directory updates and the Global Vendor Site List.
• Provides operational input and participates in operational processes in support of startup maintenance and close‑out of studies.
• Assists the GTL in driving study execution.
• Learns, observes and performs core GTA tasks and escalates appropriately.
• Facilitates vendor creation and payment processing in conjunction with the appropriate stakeholders.
• Raises possible issues for potential escalation to the appropriate colleagues.
• Follows instructions, determines level of understanding and seeks clarification when needed.
• Seeks guidance to navigate undefined tasks, challenges, and study tools/resources.
• Supports study specific CSR appendices as needed.
• Manages global vendor site lists and resolves issues related to global site lists.
• Manages study mail‑groups/​distributions and SharePoint/Study Directory updates.
• Participates, sets up agendas, and captures meeting minutes in study team meetings for assigned protocols.
• Identifies issues and risks, develops mitigations, and escalates appropriately.
• Participates in filing activities and any associated audits as applicable.
• Leads assigned study closure/archival activities during the study closure phase.

Summary

• Proactively manages multiple assignments and operational processes with moderate to minimal supervision.
• Manages country planning, protocol level attributes, and milestones/drivers in CTMS.
• Has high functional impact on the study team and the organization.

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 Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Equal Opportunity Employer

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 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: Email: [email protected].

One of our staff members will work with you to provide alternate means to submit your application.

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