Remote Evening Esl Tutor For Kids 4-11 — Fixed Hours

The Really Great Teacher Company; Quilmes; Remote; ARS 1,200,000 - 2,000,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life insurance

Flexible benefits

Job summary

ICON is seeking a motivated FSP CRA I (Entry Level) in Buenos Aires to support remote and on-site trial activities. You will perform site monitoring, coordinate documentation, and ensure adherence to ICH-GCP guidelines across sponsors and study sites.

Some travel to sites may be required. Ideal candidates hold a life sciences degree, demonstrate strong organizational skills, and communicate effectively in English.

Qualifications

• Bachelor's degree in Logistics, Supply Chain Management, or related field or equivalent experience.
• Proven experience in logistics coordination with understanding of supply chain and inventory management.
• Excellent organizational and problem-solving skills for multiple projects.
• Strong communication and interpersonal skills for cross-functional teams and partners.
• Proficiency in logistics software, data analysis tools, and Microsoft Office Suite.
• Advanced level of English

Responsibilities

• Overseeing the coordination and execution of shipments, deliveries, and inventory management for clinical trial materials.
• Developing and implementing logistics strategies to improve efficiency and reduce costs.
• Collaborating with vendors, suppliers, and internal teams to address logistics challenges.
• Monitoring and analyzing logistics performance metrics to identify opportunities for process improvements.
• Ensuring compliance with regulatory requirements and maintaining accurate shipping and inventory records.

Skills

Logistics coordination

Supply chain knowledge

Inventory management

Regulatory compliance

English proficiency

Education

Bachelor's degree in Logistics or related field

Tools

Logistics software

Data analysis tools

Microsoft Office Suite

Job description

CV Submission: Candidates must submit your CV in English . CVs in any other language will not be considered .

What You Will Be Doing:

• Overseeing the coordination and execution of shipments, deliveries, and inventory management for clinical trial materials.
• Developing and implementing logistics strategies to improve efficiency and reduce costs.
• Collaborating with vendors, suppliers, and internal teams to address and resolve logistics challenges.
• Monitoring and analyzing logistics performance metrics to identify opportunities for process improvements.
• Ensuring compliance with regulatory requirements and maintaining accurate shipping and inventory records.

Your Profile:

• Bachelor's degree in Logistics, Supply Chain Management, or a related field or equivalent experience.
• Proven experience in logistics coordination, with a strong understanding of supply chain and inventory management principles.
• Excellent organizational and problem-solving skills, with the ability to manage multiple projects and priorities.
• Strong communication and interpersonal skills, with a track record of working effectively with cross-functional teams and external partners.
• Proficiency in logistics software, data analysis tools, and Microsoft Office Suite.
• Advanced level of English

#LI-FP1
#LI-Remote

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

FSP CRA I (Entry Level) - open for Study Coordinators, aCRA and CTAs

Buenos Aires ThermoFisher Scientific

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office

Job Description
Join Us as a Clinical Research Associate I - Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you'll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You'll Do:

• Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings
• resolution. Investigates and follows-up on findings as applicable.
• Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
• Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
• Provides trial status tracking and progress update reports to the team as required. Ensures study systems are complete, accurate and updated per agreed study conventions (e.g. Clinical Trial Management System).
• Facilitates effective communication between investigative sites, the client company and internal project teams through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections.
• Maintains and completes administrative tasks such as expense reports and timesheets in a timely manner.
• Contributes to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

• Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
• Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered.
• Valid driver's license where applicable.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

• Basic medical/therapeutic area knowledge and understanding of medical terminology
• Ability to attain and maintain a working knowledge of ICH GCPs and applicable regulations and procedural documents
• Good oral and written communication skills, with the ability to communicate effectively with medical personnel
• Good interpersonal skills
• Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers' underlying issues
• Good organizational and time management skills
• Ability to remain flexibile and adaptable in a wide range of scenarios
• Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
• Ability to manage Risk Based Monitoring concepts and processes
• Ability to work in a team or independently as required
• Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
• Good English language and grammar skills

Working Conditions and Environment:

• Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
• Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.