2 Pharmaceutical Research jobs in the Philippines
Senior Research Scientist - Network Security
Manila, Metropolitan Manila
Trellix
Posted 5 days ago
Job Viewed
Job Description
**_Job Title:_**
Senior Research Scientist - Network Security
**About** **Trellix:**
**Trellix, the trusted CISO ally, is redefining the future of cybersecurity and soulful work.** Our comprehensive, GenAI-powered platform helps organizations confronted by today's most advanced threats gain confidence in the protection and resilience of their operations. Along with an extensive partner ecosystem, we accelerate technology innovation through artificial intelligence, automation, and analytics to empower over 53,000 customers with responsibly architected security solutions.
We also recognize the importance of closing the 4-million-person cybersecurity talent gap. We aim to create a home for anyone seeking a meaningful future in cybersecurity and look for candidates across industries to join us in soulful work. More at .
**_Role Overview:_**
We are looking for a Senior Research Scientist to help us build and expand
Trellix Network Detection and Response. The ideal candidate is someone who is passionate about solving real problems by turning cutting edge research into operational production solutions. In this role, you will focus on analyzing network-based attacker behavior and develop innovative solutions to address emerging challenges in the field of networking.
**Responsibilities:**
+ Research attacker methodologies and develop innovative solutions to identify detection solutions
+ Knowledge on how machine learning can be applied in networking problems
+ Perform data analysis to measure efficacy and identify methodologies to improve existing solutions
+ Forward Looking Research - Researcher will help develop leading edge prototypes to solve emerging challenges.
+ Threat Analytics - Leverage threat intelligence from different sources, identify patterns to co-relate and establish the origin and flow of attacks.
+ Drive roadmap for detection efficacy and network research operation
**Requirements:**
+ Total 8 to 14years experience with at least three years direct or equivalent experience in areas of network-based threats and other aspects of cyber attacks.
+ Strong understanding of networking protocols (e.g., TCP/IP) and network architecture.
+ Proficiency in programming languages such as Python, C++, or Java.
+ Knowledge of cybersecurity principles and practices
+ Strong analytical, problem-solving, and communication skills
**Preferred:**
+ Hands-on reverse engineering and knowledge of operating system internals.
+ Red teaming experience on various techniques
+ Machine learning experience
**Additional Qualifications**
Above all, the right passion and attitude to solve new challenges
**_Company Benefits and Perks:_**
We believe that the best solutions are developed by teams who embrace each other's unique experiences, skills, and abilities. We work hard to create a dynamic workforce where we encourage everyone to bring their authentic selves to work every day. We offer a variety of social programs, flexible work hours and family-friendly benefits to all of our employees.
+ Retirement Plans
+ Medical, Dental and Vision Coverage
+ Paid Time Off
+ Paid Parental Leave
+ Support for Community Involvement
We're serious about our commitment to a workplace where everyone can thrive and contribute to our industry-leading products and customer support, which is why we prohibit discrimination and harassment based on race, color, religion, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation or any other legally protected status.
Senior Research Scientist - Network Security
**About** **Trellix:**
**Trellix, the trusted CISO ally, is redefining the future of cybersecurity and soulful work.** Our comprehensive, GenAI-powered platform helps organizations confronted by today's most advanced threats gain confidence in the protection and resilience of their operations. Along with an extensive partner ecosystem, we accelerate technology innovation through artificial intelligence, automation, and analytics to empower over 53,000 customers with responsibly architected security solutions.
We also recognize the importance of closing the 4-million-person cybersecurity talent gap. We aim to create a home for anyone seeking a meaningful future in cybersecurity and look for candidates across industries to join us in soulful work. More at .
**_Role Overview:_**
We are looking for a Senior Research Scientist to help us build and expand
Trellix Network Detection and Response. The ideal candidate is someone who is passionate about solving real problems by turning cutting edge research into operational production solutions. In this role, you will focus on analyzing network-based attacker behavior and develop innovative solutions to address emerging challenges in the field of networking.
**Responsibilities:**
+ Research attacker methodologies and develop innovative solutions to identify detection solutions
+ Knowledge on how machine learning can be applied in networking problems
+ Perform data analysis to measure efficacy and identify methodologies to improve existing solutions
+ Forward Looking Research - Researcher will help develop leading edge prototypes to solve emerging challenges.
+ Threat Analytics - Leverage threat intelligence from different sources, identify patterns to co-relate and establish the origin and flow of attacks.
+ Drive roadmap for detection efficacy and network research operation
**Requirements:**
+ Total 8 to 14years experience with at least three years direct or equivalent experience in areas of network-based threats and other aspects of cyber attacks.
+ Strong understanding of networking protocols (e.g., TCP/IP) and network architecture.
+ Proficiency in programming languages such as Python, C++, or Java.
+ Knowledge of cybersecurity principles and practices
+ Strong analytical, problem-solving, and communication skills
**Preferred:**
+ Hands-on reverse engineering and knowledge of operating system internals.
+ Red teaming experience on various techniques
+ Machine learning experience
**Additional Qualifications**
Above all, the right passion and attitude to solve new challenges
**_Company Benefits and Perks:_**
We believe that the best solutions are developed by teams who embrace each other's unique experiences, skills, and abilities. We work hard to create a dynamic workforce where we encourage everyone to bring their authentic selves to work every day. We offer a variety of social programs, flexible work hours and family-friendly benefits to all of our employees.
+ Retirement Plans
+ Medical, Dental and Vision Coverage
+ Paid Time Off
+ Paid Parental Leave
+ Support for Community Involvement
We're serious about our commitment to a workplace where everyone can thrive and contribute to our industry-leading products and customer support, which is why we prohibit discrimination and harassment based on race, color, religion, gender, national origin, age, disability, veteran status, marital status, pregnancy, gender expression or identity, sexual orientation or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Associate
Docs Global
Posted today
Job Viewed
Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.
ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Overview:
As a Clinical Research Associate II you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team.
You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high quality results.
Key responsibilities:
- You will have the opportunity to monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas, particularly in Oncology studies.
- Assist other CRAs with co-monitoring activities both remote and on-site.
- You will utilise your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators where respect, knowledge and commitment to ICH/GCP guidelines are key to successful trial conduct.
- As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.
- You will be first to review "source to CRF/eCRF," ensuring patient safety and data integrity aspect of the study.
- As the first point of contact for study sites, escalating any concerns/issues to other departments including Safety, Investigational Medicinal Product, Local Study Managers and management team as appropriate.
- Additionally, you will oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct.
Required experience and qualifications:
- Bachelor’s Degree (or equivalent) with minimum 2 years or more of relevant healthcare monitoring experience in the pharma or clinical research industry.
- Proficiency with medical terminology
- Working knowledge of Local Regulations
- A demonstrated working knowledge of ICH/GCP Guidelines
- Excellent record-keeping skills and attention to detail
- Experience conducting Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site
- Strong technical skills with CTMS, eCRF, eTMF
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.
In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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.
CRAjob
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success.
ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Overview:
As a Clinical Research Associate II you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team.
You will be managing competing priorities, supporting the on-site team, ensuring investigators follow the clinical trial protocol, providing training, and most importantly, motivating the team to ensure high quality results.
Key responsibilities:
- You will have the opportunity to monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas, particularly in Oncology studies.
- Assist other CRAs with co-monitoring activities both remote and on-site.
- You will utilise your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators where respect, knowledge and commitment to ICH/GCP guidelines are key to successful trial conduct.
- As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely.
- You will be first to review "source to CRF/eCRF," ensuring patient safety and data integrity aspect of the study.
- As the first point of contact for study sites, escalating any concerns/issues to other departments including Safety, Investigational Medicinal Product, Local Study Managers and management team as appropriate.
- Additionally, you will oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct.
Required experience and qualifications:
- Bachelor’s Degree (or equivalent) with minimum 2 years or more of relevant healthcare monitoring experience in the pharma or clinical research industry.
- Proficiency with medical terminology
- Working knowledge of Local Regulations
- A demonstrated working knowledge of ICH/GCP Guidelines
- Excellent record-keeping skills and attention to detail
- Experience conducting Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site
- Strong technical skills with CTMS, eCRF, eTMF
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.
In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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.
CRAjob
This advertiser has chosen not to accept applicants from your region.
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