Sr. Project Specialist - Buenos Aires Hybrid

Posted 18 Days Ago
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Buenos Aires, Ciudad Autónoma de Buenos Aires, ARG
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
The Sr. Project Specialist manages study/project planning and execution using performance metrics, assists in documentation accuracy, and facilitates communication among cross-functional teams while addressing issues and ensuring compliance with study protocols.
Summary Generated by Built In
Sr. Project Specialist - Buenos Aires Hybrid

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
 
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
 
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 deliver – for one another, our customers, and, most importantly, for those in need.
 
Discover what your 25,000 future colleagues already know:
 
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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. 
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. 

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 support 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 etc. 
• Provides operational input and participates in operational processes in support of startup maintenance and close out of studies. 
• Assist 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 resolve 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.
• Lead assigned study closure/archival activities during study closure phase

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.

http://www.syneoshealth.com

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.

Skills Required

  • Experience in project management, specifically in clinical trials or drug development
  • Strong organizational and communication skills
  • Ability to work effectively in cross-functional teams
  • Familiarity with eTMF and SharePoint tools

Syneos Health Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Syneos Health and has not been reviewed or approved by Syneos Health.

  • Leave & Time Off Breadth Unlimited PTO for managers and flexible time‑off options make time away accessible and support work‑life balance. Day‑to‑day usability can depend on team and workload, but the policy breadth is a clear strength.
  • Retirement Support A 401(k) with company match is frequently highlighted as a strong component of the package. Despite vesting details to confirm, the retirement offering adds meaningful long‑term value.
  • Parental & Family Support Partnership with Maven provides fertility, adoption support, parental‑leave guidance, and women’s health resources across multiple regions. This family‑building support enhances the overall total rewards appeal.

Syneos Health Insights

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The Company
HQ: Morrisville, NC
22,543 Employees

What We Do

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. We bring together a talented team of professionals, who work across more than 110 countries, with a deep understanding of patient and physician behaviors and market dynamics. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. Syneos Health supports a diverse, equitable and inclusive culture that cares for colleagues, customers, patients, communities and the environment.

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