NTT America, Inc.

Hoy

Partially Remote

Lima, Peru

Full time

R-65159

Who We Are

At Kyndryl, we run and reimagine the mission‑critical technology systems that drive advantage for the world's leading businesses. We are at the heart of progress; with proven expertise and a continuous flow of AI‑powered insight, enabling smarter decisions, faster innovation, and a lasting competitive edge. For our people‑Kyndryls that means doing purposeful work that powers human progress. Join us and experience a adaptable, supportive environment where your well‑being is prioritized and your potential can thrive.

The Role

Your role

Bring your specialist knowledge and experience to a company managing 50% of the world's MIPS and play a critical role in our modernization mission. You'll be in good company among our global community of experts leading the future of mainframe modernization. Experts who share knowledge openly and collaborate freely.

What you will do

- Maintain Performance: Prevent decay and find efficiencies: Monitor the architecture and identify opportunities to optimize code to maintain and enhance mainframe performance.
- Debug and Test: Find and fix: Debug, troubleshoot, and analyze complex system interactions to keep mission‑critical applications running.
- Develop for the Future: Bridge the gap: As an instrumental player in modernization, you'll extract business logic from legacy systems for migration or integration with cloud‑based services.

Who You Are

Required skills and experience

- Experience working as a software engineer on complex software projects.
- Excellent coding skills and solid development experience (Java, Springboot, Quarkus, GraphQL, Kafka, SpringBatch, ApacheFlink) with debugging and problem‑solving skills.
- Software development methodologies, with demonstrated experience developing scalable and robust software.
- Experienced in relational and NoSQL databases, data mapping, XML/JSON, REST‑based web services.
- Knowledge of architecture design - Microservices architecture, containers (Docker & AKS), messaging queues.
- Deep understanding of OOP and design patterns.
- Azure Components

Preferred skills and experience

- Bachelor's degree in Computer Science, related technical field, or equivalent practical experience.
- Certification in one or more of the hyperscalers (Azure, AWS, and Google GCP) - otherwise, you can obtain certifications with Kyndryl.
- Experience with DevOps tools and modern engineering practices.

Being You

The "Kyn" in Kyndryl means kinship, which represents the strong bonds we have with each other, our customers and our communities. We focus on ensuring all Kyndryls feel included and we welcome people of all cultures, backgrounds, and experiences. Even if you don't meet every requirement, we encourage you to apply. We believe in growth, and we're excited to see what you can bring. At Kyndryl, employee feedback has told us that our number one driver of employee engagement is belonging. That sense of belonging - being a valued, respected, trusted member of the team - is fundamental to our culture and fueling great experiences for our customers. This dedication to welcoming everyone into our company means that Kyndryl gives you the ability to thrive and contribute to our culture of empathy and shared success. That's The Kyndryl Way.

What You Can Expect

Your career with us isn't just a job-it's an adventure with purpose. We offer a dynamic, hybrid‑friendly culture that supports your well‑being and empowers you to grow. Our Be Well programs are thoughtfully designed to support your financial, mental, physical, and social health-because we know that when you feel your best, you do your best.

From your very first day, you'll dive into impactful work that powers the systems our customers rely on every day. You won't just contribute-you'll make a difference, tackling meaningful projects that sharpen your skills and fuel your growth.

We're here to champion your journey. With powerful tools to chart your career path, personalized development goals aligned with your ambitions, and continuous feedback to keep you inspired and on track,



you'll have everything you need to thrive and evolve. You'll develop in‑demand skills to grow your career and achieve your ambitions with access to cutting‑edge learning opportunities-from certifications with Microsoft, Google, and Amazon to coaching and hands‑on experiences.

And through it all, you'll be part of a culture that values empathy, restless learning, and a devotion to shared success.

We want you to thrive here-and we're committed to helping you do just that. Ready to make an impact? Join us and help shape what's next.

Kyndryl is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics. Kyndryl is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Senior Clinical Research Associate/Clinical Research Associate - FSP

Parexel FSP is actively hiring multiple Clinical Research Associates and Senior Clinical Research Associates to join our growing team.

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study.

The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies, in compliance with Client Procedural Documents, international guidelines such as ICH‑GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.

Key Accountabilities

Site Management Responsibilities

- Contributes to the selection of potential investigators.
- In some countries, as required, CRAs are accountable for study start‑up and regulatory maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start‑up and for the duration of the study.
- Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles.
- Confirms that site staff have completed and documented the required training appropriately, including ICH‑GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times.
- Actively participates in Local Study Team (LST) meetings.
- Contributes to National Investigators meetings, as applicable.
- Initiates, monitors, and closes study sites in compliance with Client Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST.
- Drives performance at the sites. Proactively identifies and ensures timely resolution to study‑related issues and escalates them as appropriate.
- Updates CTMS and other systems with data from study sites as per required timelines.
- Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable.
- Performs monitoring visits (remote and onsite), as well as remote data checks,



in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines, and discusses with LSAD the correct timing and type of visits.
- Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan.
- Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study.
- Ensures data query resolution in a timely manner.
- Works with data management to ensure robust quality of the collected study data.
- Ensures accurate and timely reporting of Serious Adverse Events and their follow ups.
- Prepares and finalizes monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow‑up letter, within required timelines and in line with Client SOP.
- Follows up on outstanding actions with study sites to ensure resolution in a timely manner.
- Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH‑GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required.
- Assists site in maintaining inspection ready ISF.
- Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD).
- Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICH‑GCP, Client SOPs and local requirements. Supports/participates in regular QC checks performed by LSAD or delegate.
- Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc.) are available and ready for final archiving and completion of local part of the eTMF.
- Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
- Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line manager.

Compliance with Sponsor Standards

- Ensures compliance with the Client's Code of Ethics and company policies and procedures relating to people, finance, technology, security, and SHE (Safety, Health and Environment).
- Ensures compliance with local, national, and regional legislation, as applicable.
- Completes timesheets accurately as required.

Compliance with Parexel Standards

- Complies with required training curriculum.
- Completes timesheets accurately as required.
- Submits expense reports as required.
- Updates CV as required.
- Maintains working knowledge of and complies with Parexel/Client processes, ICH‑GCPs and other applicable requirements.

Skills (Essential):

- Proficient in written and spoken English language required.
- Fluency in local language(s) required.

Knowledge and Experience (Essential)

- Excellent knowledge of international guidelines ICH‑GCP, basic knowledge of GMP/GDP.
- Good knowledge of relevant local regulations.
- Good medical knowledge and ability to learn relevant Client Therapeutic Areas.
- Basic understanding of the drug development process.
- Good understanding of Clinical Study Management including monitoring, study drug handling and data management.
- 3+ years of experience as an on‑site Clinical Research Associate (CRA) for the Senior CRA position and 1+ years of experience for the Clinical Research Associate role.

Education:

- Bachelor's degree in related discipline, preferably in life science, or equivalent qualification (adapted to local country market needs), that supports skills and capabilities of the position and ensures successful conduct of responsibilities and appropriate interactions with internal and or external customers.

Other:

- Ability to travel nationally/internationally as Required

#LI‑LG4

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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