Remote Lead Gen Specialist - Part-Time, Growth & Perks

Vontier Corporation; Quilmes; Remote; ARS 108,178,000 - 139,086,000; Full time

Job summary

IQVIA seeks a Senior Site Activation Specialist, ICF Lead, to manage country-level SA activities within LATAM from a homebased setting. You will act as SPOC for assigned studies, coordinating with sites, SAMs, PM teams, and stakeholders to ensure regulatory and contractual milestones are met.

You bring a life sciences degree and at least 3 years in clinical research, with strong regulatory knowledge and cross-functional collaboration.

Qualifications

• Bachelor's degree in Life Sciences or a related field (required).
• Minimum of 3 years of clinical research or relevant experience.
• Strong understanding of country-specific regulatory requirements within LATAM.
• Demonstrated ability to manage multiple priorities, meet deadlines, and work cross-functionally.
• Strong communication skills, attention to detail, and problem-solving mindset.

Responsibilities

• Serve as SPOC for assigned studies with sites and teams.
• Ensure compliance with local regulations and SOPs.
• Perform feasibility assessments and site activation activities.
• Prepare and review site documentation for accuracy and timeliness.
• Maintain data in internal systems and tracking tools.
• Provide local regulatory and operational expertise to teams.

Skills

Communication skills

Project coordination

Regulatory knowledge

Multi-tasking

Education

Bachelor's degree in Life Sciences or related field

Job description

Buenos Aires, Argentina
Full time
R

Site Activation Specialist, ICF Lead

Location: LATAM
Work Model: Homebased

Job Overview

The Site Activation Specialist, ICF Lead performs country-level Site Activation (SA) activities in compliance with applicable local and international regulations, IQVIA Standard Operating Procedures (SOPs), project requirements, and contractual or budgetary guidelines.
This role is a senior individual contributor position, operating under moderate supervision, with responsibility for managing key start-up deliverables and providing local and regional expertise . The role also contributes to continuous improvement by making recommendations to enhance processes, systems, and operational effectiveness within Site Activation.

Essential Functions

+ Under general supervision, act as the Single Point of Contact (SPOC) for assigned studies, collaborating with investigative sites, Site Activation Managers (SAMs), Project Management teams, and other internal stakeholders
+ Ensure compliance with local regulations , SOPs, Work Instructions (WIs), quality standards, and agreed project timelines
+ Perform feasibility assessments, site identification, study start-up, and site activation activities in line with regional regulatory requirements
+ Prepare, review, and distribute site documentation, ensuring completeness, accuracy, and timeliness
+ Maintain accurate and up-to-date information in internal systems, databases, and tracking tools
+ Review site performance metrics and provide insights and feedback to management
+ Review, establish, and align on project plans and timelines , ensuring monitoring measures and contingency plans are implemented when needed
+ Communicate completion of feasibility, site identification, regulatory, and contractual milestones to relevant project team members
+ Review, track, and follow up on the progress, approval, and execution of study documents, including:
+ Confidential Disclosure Agreements (CDAs)
+ Site Information Forms (SIFs)
+ Regulatory and ethics submissions
+ Informed Consent Forms (ICFs)
+ Investigator Packs (IPs) and IP release documentation
+ Provide local regulatory and operational expertise to SAMs and project teams during start-up and throughout study execution
+ Perform quality control reviews of documentation received from investigative sites
+ Maintain limited and appropriate direct sponsor contact for specific initiatives, as required

Qualifications

+ Bachelor's degree in Life Sciences or a related field (required)
+ Minimum of 3 years of clinical research or relevant experience , or an equivalent combination of education, training, and experience
+ Strong understanding of country-specific regulatory requirements within one or more of the listed locations
+ Demonstrated ability to manage multiple priorities, meet deadlines, and work cross-functionally
+ Strong communication skills, attention to detail, and problem‑solving mindset
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

The SYSS Engineering Group in Latin America provides fully engineered control system solutions for power and process plants in the Americas. The group focuses on installing and replacing plant control systems with Emerson DCS's (Delta V & Ovation), Reliability and SCADA Solutions providing engineering design, system integration, testing and commissioning services to deliver comprehensive solutions to our customers. The successful candidate will be an essential part of the group with responsibilities of participating in projects supporting regional offices such us Brazil, Mexico, Argentina and also US Offices.
In This Role, Your Responsibilities Will Be:
Project Engineer role:
With minimal direction can design some non-complex solutions.
+ Designs and implements hardware database, logics, graphics and datalinks.
+ With guidance selects hardware and software for project implementation.
+ Review application documentation for quality, accuracy and completeness.
+ Work closely with project technical leader/s to verify the project requirements are met accordingly.
+ Solve technical problems through the combination of standard procedures, modifications of standard procedures, experience, or methods developed in previous assignments.
+ Work closely with partners to meet the project requirements and deadlines.
+ Consistently shows ability to accurately communicate with customers.
+ Constantly works proactively and independently.
+ Successful execution of assigned projects/services and ensure high customer satisfaction.
+ Execute project tasks/site services according to quality, delivery date and assigned budget.
+ Lead product enhancement and product definitions when required by Innovative Projects
+ Lead activities like factory acceptance testing, site acceptance testing, commissioning, and startup.
+ Perform high expertise activities like loop tuning, turbine startups, advanced controls, prediction solutions and also support implementation of performance solutions.
+ Technical Lead role: Lead implementation team that works in different plant processes and applications (O&G, Chemical, Mining Power, etc.) participating in the project phases such as In-house Engineering, FAT and SAT).
+ Successful execution of assigned projects and ensure high customer satisfaction.
+ Supervise Subcontractors during Engineering, and Commissioning Phases
+ Responsible of Functional Design (Hardware and Software) including reverse Engineering in Retrofit Projects
+ Develop Implementation and Commissioning Plans and align them with Project Requirements
+ Supervise Remote Engineering teams (India, Cluj, others) of big projects being able to oversee a groups of 25-30 Engineers
+ Promote Adoption of Productivity tools as well as