ABOUT NOGIGIDDY

NoGigiddy is a digital platform built for gig workers, side hustlers, and anyone building an income outside the traditional 9-to-5. We connect our community with real earning opportunities — remote jobs, surveys, clinical trials, gig platforms, and financial tools — all in one place, free to access, no gatekeeping. We built what we wish had existed, and we hire people who actually get it.

THE ROLE

The future of AI is being built right now — and the humans labeling the data are the ones making it possible. NoGigiddy is hiring Data Annotators to help train the next generation of machine learning models. You'll review, tag, and classify text, images, audio, and video so that AI systems can learn to understand the world. No tech background required — just sharp attention to detail and the ability to follow clear guidelines consistently.

RESPONSIBILITIES

Review and label datasets including text, images, audio clips, and video frames according to provided guidelines

Categorize content accurately across a range of annotation tasks (sentiment, object detection, intent classification, etc.)

Flag ambiguous or problematic content for senior review

Meet quality benchmarks — accuracy matters more than speed

Complete tasks within assigned deadlines while maintaining consistency

Provide feedback on annotation guidelines when instructions are unclear or contradictory

ABOUT NOGIGIDDY

NoGigiddy is a digital platform built for gig workers, side hustlers, and anyone building an income outside the traditional 9-to-5. We connect our community with real earning opportunities — remote jobs, surveys, clinical trials, gig platforms, and financial tools — all in one place, free to access, no gatekeeping. We built what we wish had existed, and we hire people who actually get it.

THE ROLE

The future of AI is being built right now — and the humans labeling the data are the ones making it possible. NoGigiddy is hiring Data Annotators to help train the next generation of machine learning models. You'll review, tag, and classify text, images, audio, and video so that AI systems can learn to understand the world. No tech background required — just sharp attention to detail and the ability to follow clear guidelines consistently.

RESPONSIBILITIES

Review and label datasets including text, images, audio clips, and video frames according to provided guidelines

Categorize content accurately across a range of annotation tasks (sentiment, object detection, intent classification, etc.)

Flag ambiguous or problematic content for senior review

Meet quality benchmarks — accuracy matters more than speed

Complete tasks within assigned deadlines while maintaining consistency

Provide feedback on annotation guidelines when instructions are unclear or contradictory

ABOUT NOGIGIDDY

NoGigiddy is a digital platform built for gig workers, side hustlers, and anyone building an income outside the traditional 9-to-5. We connect our community with real earning opportunities — remote jobs, surveys, clinical trials, gig platforms, and financial tools — all in one place, free to access, no gatekeeping. We built what we wish had existed, and we hire people who actually get it.

THE ROLE

The future of AI is being built right now — and the humans labeling the data are the ones making it possible. NoGigiddy is hiring Data Annotators to help train the next generation of machine learning models. You'll review, tag, and classify text, images, audio, and video so that AI systems can learn to understand the world. No tech background required — just sharp attention to detail and the ability to follow clear guidelines consistently.

RESPONSIBILITIES

Review and label datasets including text, images, audio clips, and video frames according to provided guidelines

Categorize content accurately across a range of annotation tasks (sentiment, object detection, intent classification, etc.)

Flag ambiguous or problematic content for senior review

Meet quality benchmarks — accuracy matters more than speed

Complete tasks within assigned deadlines while maintaining consistency

Provide feedback on annotation guidelines when instructions are unclear or contradictory

About the Job

Excelya invites you to join a team defined by Audacity, Care, and Energy. We foster bold innovation and support a collaborative environment where personal and professional growth thrive.

As a Clinical Research Associate at Excelya, you will be integral to ensuring the successful execution of clinical trials by overseeing site activities, adherence to protocols, and regulatory compliance. This role is pivotal in advancing clinical projects that aim to improve patient care.

Main Responsibilities:

• Conduct site initiation, monitoring, and close-out visits to ensure compliance with clinical trial protocols.
• Maintain effective communication with investigators and site staff to support trial progress.
• Review and verify clinical trial data and documentation for accuracy and completeness.
• Monitor patient safety and data integrity throughout the study duration.
• Assist in preparation for audits and inspections, ensuring sites are inspection-ready.
• Report deviations, adverse events, and other study-related issues in a timely manner.
• Collaborate with project managers to provide updates and address challenges encountered at sites.

Requirements

Requirements:

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities:

• Perform monitoring of international clinical trials across Phases I–IV, ensuring protocol adherence and data integrity at investigational sites.
• Guarantee scientific, regulatory, and technical quality through meticulous oversight and application of GCP and local regulatory standards.
• Manage investigational product (IP) logistics including reconciliation, storage, dispensing, and inventory, with special focus on blinded/randomized protocols.

Beyond that, you will also be able to:

About the Job

Join Excelya as a Vendor Manager Biocollection, where Audacity, Care, and Energy define who we are and how we work. This role is essential in managing vendor relationships specifically related to biocollection processes to ensure the highest quality and compliance in clinical studies.

Main Responsibilities:

• Manage and coordinate biocollection vendors throughout all phases of clinical trials.
• Negotiate contracts, monitor vendor performance, and ensure compliance with regulatory requirements and study protocols.
• Collaborate closely with internal teams and external partners to align expectations and timelines.
• Ensure proper documentation, data transfer, and timely resolution of issues related to biocollection activities.
• Support risk assessment and mitigation plans regarding biocollection vendors.
• Contribute to study kick-off meetings, vendor selection processes, and contract management.

Requirements

About You

About the Job

We are seeking a Data Manager Support to assist the Data Management team in ensuring the accuracy, integrity, and quality of clinical trial data throughout the study lifecycle.

The role focuses on assessing data quality, measuring FAIRness, reinforcing data integrity, and supporting referential data controls, while contributing to reporting, documentation, and dashboarding activities.

Main Responsibilities:

• Assess data quality within the defined scope and identify areas for improvement.
• Measure and document the FAIRness (Findable, Accessible, Interoperable, Reusable) of data assets.
• Contribute to Data Integrity analyses of critical business and technical processes.
• Document data assets and processes using ad‑hoc tools such as data catalogs and data contracts.
• Implement and monitor data quality controls on referential data managed by the department.
• Contribute to dashboarding and automation initiatives to support data monitoring and reporting.
• Produce monthly activity reports and deliver mission‑related documentation in line with applicable procedures.

Requirements

About You

About the Job

Excelya is seeking a skilled Pharmacokineticist to join our dynamic team. You will play a key role in supporting the pharmacokinetic (PK) evaluation of clinical trials across all phases, contributing to drug development and regulatory submissions.

The consultant will contribute to pharmacokinetics (PK) activities across Phase I to Phase III clinical trials, ensuring the timely delivery of high‑quality PK analyses, interpretations, and documentation.

Key Responsibilities:

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We are committed to creating innovative solutions and fostering a collaborative and inclusive work environment.

The consultant will contribute to pharmacokinetics (PK) activities across Phase I to Phase III clinical trials, ensuring the timely delivery of high‑quality PK analyses, interpretations, and documentation. This role involves close collaboration with clinical, non-clinical, and modeling teams to deliver robust pharmacokinetic data and modeling outputs that inform drug dosing strategies and regulatory submissions.

Main responsibilities:

Senior Clinical Project Manager

At Excelya, we are seeking an experienced Senior Clinical Project Manager to lead and oversee complex clinical trials from initiation to close-out, ensuring adherence to timelines, budgets, and quality standards. This role offers the opportunity to work within a vibrant team focused on delivering impactful clinical research in a collaborative and innovative environment.

Key Responsibilities:

• Lead and coordinate oncology clinical studies from set‑up to close‑out
• Contribute to protocol and clinical document writing
• Manage timelines, budgets, regulatory submissions, and study deliverables
• Coordinate internal and external stakeholders (sites, CRAs, partners)
• Ensure patient safety, data quality, and regulatory compliance
• Organize project meetings, reporting, and performance tracking
• Supervise and support project teams (CRAs, study coordinators)

Requirements

Requirements: