ICON Strategic Solutions | Clinical Research Associate II
Há 13 horas
You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent communication, both internally and with our client, positions our program to be closely aligned on our shared goals.
The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference on Harmonization Good Clinical Practices (ICH-GCP) and all applicable regulatory requirements.
- Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, providing instructions to site personnel and study close out.
- Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in
- Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable
- Manages the investigative site staff to facilitate trial deliverables, e.g., subject enrollment, data deliverables.
- Verifies proper management and accountability of Investigational Product (IP).
- Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed
- Manages essential documents as required by local regulations and ICH-GCP guidelines before, during and after a clinical study; assists with resolution of investigational site/data queries.
- Performs key risk assessment and management responsibilities throughout the project, including key risk indicator and site health analysis, site process evaluation, and project escalation.
- Participates in audit preparation and follow-up activities as needed.
- Independently performs a variety of onsite and offsite monitoring visit types.
- Gathers and reviews information for assigned siteand identifies inconsistencies. With limitedguidance from project and
- Assists with non-complex adhoc, short-term assignmentin support of additional studies or departmental initiatives.
- May serve as preceptor, providing training to less experienced clinical team members.
- Undergraduate degree or international equivalent in clinical, science, or healthrelated field from an accredited institution; health care professional licensure, i.e., registered nurse
- Previous experience supporting clinical trials including solid on-site monitoring experience.
- Travel is required 50-80%
- Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write and speak fluent English and host country language.
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.
Visit our careers website to read more about the benefits of working at ICON: ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
-
Clinical Trials Associate
4 semanas atrás
Brasil ICON Strategic Solutions Tempo inteiroJob Title: Sr Clinical Research Associate | ICON Strategic SolutionsAbout the Role: As a Clinical Research Associate at ICON Strategic Solutions, you will play a vital role in the success of our clinical trials. Your responsibilities will include onsite and remote monitoring activities, ensuring patient safety and data integrity.Key...
-
Clinical Research Associate II
1 dia atrás
Brasil ICON Strategic Solutions Tempo inteiroA Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent...
-
Clinical Research Associate
Há 1 mês
Brasil ENGINEERINGUK Tempo inteiroClinical Research Associate Role SummaryAt ENGINEERINGUK, we are seeking a highly skilled Clinical Research Associate to contribute to our accelerated drug/device/outcomes research program. As a Clinical Research Associate, you will play a critical role in ensuring patient safety and data integrity through independent monitoring of studies.Key...
-
Clinical Research Associate
Há 23 horas
Brasil ENGINEERINGUK Tempo inteiroUnlock the Future of Medicine as a Clinical Research Associate with ENGINEERINGUKAbout the Role:We are seeking an experienced Clinical Research Associate to join our team in São Paulo, Brazil. As a key member of our research team, you will be responsible for monitoring the progress of clinical studies at investigative sites or remotely, ensuring that trials...
-
Clinical Research Associate
3 semanas atrás
Brasil ENGINEERINGUK Tempo inteiroAbout the RoleWe are seeking an experienced Clinical Research Associate to join our team in São Paulo. As a key member of our clinical research team, you will play a critical role in ensuring the success of our drug and device development projects.
-
Senior Clinical Research Associate
1 semana atrás
Brasil Syneos Health, Inc. Tempo inteiroAt Syneos Health, we are dedicated to accelerating customer success in the biopharmaceutical industry. As a Senior Clinical Research Associate II with our company, you will be responsible for performing site qualification, site initiation, interim monitoring, and close-out visits to ensure regulatory compliance.The estimated annual salary for this position...
-
Clinical Operations Lead
3 semanas atrás
Brasil IQVIA Tempo inteiroIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.We are seeking an experienced Clinical Operations Lead to join our team in Brazil. As a key member of our clinical operations team, you will be responsible for ensuring the successful management, performance, and career...
-
Clinical Research Associate
4 semanas atrás
Brasil Engineeringuk Tempo inteiroAbout the RoleAt Engineeringuk, we're seeking a highly skilled Clinical Research Associate to join our team in Brasilia or Goiania. As a key member of our clinical trials department, you will play a vital role in ensuring patient safety and data integrity.Job SummaryThis is an exciting opportunity to work on accelerated drug/device/outcomes research...
-
Clinical Research Operations Director
Há 4 horas
Brasil IQVIA Tempo inteiroAbout the RoleWe are seeking an experienced Clinical Research Operations Director to lead our life sciences team. As a key member of our operations team, you will be responsible for ensuring the successful management and performance of our clinical research associates and monitor staff.This is an excellent opportunity to leverage your expertise in clinical...
-
Advanced Clinical | Sr Clinical Trial Manager | brasil
3 semanas atrás
brasil Advanced Clinical Tempo inteiroFreelance Clinical Trial Manager looking after LATAM Oncology-focused Midsized Pharma Company The role will focus on vendor management and site engagement in LATAM for the Phase III global clinical trial. Summary The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH...
-
Advanced Clinical | Sr Clinical Trial Manager | brasil
3 semanas atrás
brasil Advanced Clinical Tempo inteiroFreelance Clinical Trial Manager looking after LATAMOncology-focused Midsized Pharma Company The role will focus on vendor management and site engagement in LATAM for the Phase III global clinical trial.SummaryThe Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH...
-
Senior Clinical Research Associate
Há 1 mês
Brasil Syneos Health, Inc. Tempo inteiro{"Responsibilities": "As a Senior Clinical Research Associate at Syneos Health, you will be responsible for ensuring the successful conduct of clinical trials at investigator sites. This includes site qualification, initiation, monitoring, and close-out visits. You will verify the process of obtaining informed consent and ensure regulatory compliance with...
-
Sr Clinical Trial Manager
3 semanas atrás
Brasil Advanced Clinical Tempo inteiroFreelance Clinical Trial Manager looking after LATAM Oncology-focused Midsized Pharma Company The role will focus on vendor management and site engagement in LATAM for the Phase III global clinical trial. Summary The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH...
-
Clinical Research Coordinator
4 semanas atrás
Brasil ENGINEERINGUK Tempo inteiroJob DescriptionAs a Clinical Trial Assistant at ENGINEERINGUK, you will play a vital role in the success of our clinical trials. Your primary responsibility will be to perform investigative site recruitment and feasibility, essential document collection and review, clinical status tracking, and in-house site management activities in accordance with the...
-
Clinical Research Coordinator Role in Oncology Study
3 semanas atrás
Brasil Hobson Prior Tempo inteiroJob OverviewHobson Prior is a reputable organization seeking a skilled Clinical Research Coordinator for an oncology study in Porto Alegre, Brazil.
-
Strategic Business Growth Associate
4 semanas atrás
Brasil Storydoc Technologies LTD Tempo inteiroBusiness Development and Marketing Research Intern RoleWe're a remote-first startup that redefines online business communications, leveraging interactive presentations to captivate leads.As a Business Development and Marketing Research Intern, you'll play a pivotal role in our growth journey. Your tasks will include researching and identifying new business...
-
Strategic Zoho Solutions Architect
3 semanas atrás
Brasil Clear Summit Group Tempo inteiroAbout the RoleWe are seeking an experienced Strategic Zoho Solutions Architect to join our team at Clear Summit Group. This is a full-time remote role that requires strong communication skills, project management expertise, and a passion for problem-solving.
-
Head of Primary Research
Há 1 mês
Brasil Multipolitan Tempo inteiroCompany Description: Multipolitan is the world’s first product-driven global migration platform, simplifying travel, relocation, business setup, and asset management for global citizens. With offices in Dubai and Singapore, we help families navigate geopolitical risks, capitalize on global opportunities, and achieve financial resilience through...
-
Head of Primary Research
Há 1 mês
brasil Multipolitan Tempo inteiroCompany Description:Multipolitan is the world’s first product-driven global migration platform, simplifying travel, relocation, business setup, and asset management for global citizens. With offices in Dubai and Singapore, we help families navigate geopolitical risks, capitalize on global opportunities, and achieve financial resilience through...
-
Head of Primary Research
Há 1 mês
Brasil, BR Multipolitan Tempo inteiroCompany Description:Multipolitan is the world’s first product-driven global migration platform, simplifying travel, relocation, business setup, and asset management for global citizens. With offices in Dubai and Singapore, we help families navigate geopolitical risks, capitalize on global opportunities, and achieve financial resilience through...
