206 Cra jobs in the Philippines

JOB SUMMARY:

• Customer Relations Assistant

The Customer Relations Assistant will be assisting clients primarily in opening deposit or investment accounts, as well as cross-selling the Bank's products and services.

• Teller

The Teller will be responsible for ensuring client satisfaction through friendly and efficient servicing of deposits, withdrawals, bills and loan payments.

JOB QUALIFICATIONS:

• Candidate must possess at least a Bachelor's/College Degree , Economics, Finance/Accountancy/Banking, Human Resource Management, Business Studies/Administration/Management, Marketing or equivalent.
• No work experience required.
• Fresh graduates and entry-level applicants are encouraged to apply
• Full-Time position(s) available.

Company Background

PicnicHealth is simplifying clinical research with AI, making it faster and cheaper to get new treatments to patients. We're bringing a patient-centered, AI-first approach to a $100b market otherwise dominated by old-school, services-driven incumbents. We're creating a streamlined operating system for clinical research, built on top of our AI for medical record data in trials and a personal health assistant that keeps patients engaged (NPS 66).

Our Cebu, Philippines office plays a vital role in our operations, housing a dedicated team of medical processors, including medical allied professionals, US Registered Nurses (USRNs), and Medical Records Retrieval Representatives. Their expertise and commitment significantly impact our mission, ensuring that we provide accurate and comprehensive medical records to our users.

At PicnicHealth, we are committed to transforming healthcare through technology and collaboration. Join us in our journey to reshape the healthcare landscape 

Job Brief

We are looking for a
Clinical Research Associate

to join our team and act as a point of contact for all clinical escalations.

As a Clinical Research Associate, you are responsible for reviewing patient medical records to determine if they meet study inclusion criteria, working with physician researchers on developing cohort specifications and protocols, and providing clinical expertise to help chart abstractors accurately extract and structure key medical concepts from patient records. We're seeking an experienced research nurse to join the team to provide clinical and clinical research expertise as we continuously strive to improve our data and expand into new disease areas.

Responsibilities

• Research and Escalation
• Triage clinical issues coming from our trained chart abstractors or analytics teams
• Anticipation and coordination of regulatory issues, clinical data oversight and quality assurance monitoring
• Work with a cross-functional team to define and clarify clinical requirements, help develop analysis plans, and ensure data quality standards.
• Assure consistency in research protocols
• Document and modify operational protocols
• Facilitate fortnightly calibration sessions in partnership with quality control team
• Handle and resolve escalations in an accurate and timely manner
• Support training by providing clinical context

Requirements

• Graduate of Bachelors of Science in Nursing
• With an active US RN license
• 2+ years in a clinical research nurse role + 2+ years in a clinical setting
• Sound decision making and organizational skills
• Ability to present complex information to a variety of audiences

As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a 'career ceiling.' You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. And you won't do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits.

Your responsibilities will include:

• Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements.

Qualifications:

• University degree in scientific discipline or healthcare
• At least 1 year of on-site monitoring experience
• Good knowledge of GCP and clinical research regulatory requirements
• Good computer skills including MS Office
• Excellent command of English language
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with colleagues, managers, and customers.
• Flexibility to travel.

What you can expect:

• Working with different customers on global trials
• Career development opportunities for those who are passionate in wanting to grow as part of the organization.
• Leaders that support flexible work schedules/arrangement
• Excellent working environment in a stable, international, reputable company
• Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
• Attractive remuneration package.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more

About the Role

We're looking for a roll-up-your-sleeves clinical research professional who can bridge CRA site monitoring, data entry/quality checks, and day-to-day clinical operations. In a startup environment, no two days look the same — one day you'll be at a site monitoring source documents, the next you'll be troubleshooting an EDC query, and the next you'll be helping track enrollment or prep for a regulatory submission.

This role is for someone who thrives in a fast-moving, hands-on environment and wants to make an impact by keeping trials running smoothly, data clean, and operations on track.

What You'll Do

● Site Monitoring & Support

■    Conduct site visits (initiation, monitoring, close-out) and keep sites aligned with protocol and GCP.

■    Verify source data and help resolve queries quickly.

■    Provide training and serve as a go-to for site staff.

● Data Entry & Quality

■    Enter and review clinical data in EDC.

■    Spot issues and inconsistencies early and follow through to resolution.

■    Help keep data flowing on time and accurate.

● Clinical Ops Oversight

■    Support study start-up (reg docs, IRB/EC submissions, site set-up).

■    Maintain study files and trackers (eTMF, logs, spreadsheets).

■    Track enrollment, timelines, and key milestones.

■    Jump in wherever needed — from vendor coordination to preparing reports for leadership.

What You Bring

● –4 years in clinical research (CRA, coordinator, or clinical ops).

● Strong knowledge of GCP and basic regulatory requirements.

● Comfortable with EDC, eTMF, and Excel/Google Sheets.

● Sharp eye for detail and love of clean data.

● A problem-solver who doesn't wait to be told what to do.

● Excited by startup life — resourceful, adaptable, and collaborative.

Bonus Points

● Experience in oncology, imaging, or medical devices.

● Prior exposure to risk-based monitoring.

● Familiarity with dashboards, trackers, or clinical ops tech.

Why Join Us

You'll be at the heart of a small, mission-driven team pushing forward clinical innovation. We offer the chance to wear multiple hats, learn across functions, and see the direct impact of your work on study success.

Apply Here

Company Overview:

Our client is a Philippine pharmaceutical company established in 2005 to provide affordable, world-class specialty prescription medicines for Filipinos. The company specializes in branded generics and branded medicines for various medical fields, including Central Nervous System, Endocrine disorders, Diabetes, Ob-gyn, Urology, Nephrology, and Ophthalmology. Their Vision is to improve the quality of life for Filipinos by making high-quality, accessible healthcare solutions more affordable and accessible nationwide.

Job Summary:

We are seeking a highly detail-oriented and analytical Data Management Specialist to ensure the integrity, accuracy, and security of our organization's data assets. This role involves managing data collection, storage, organization, and analysis to support business operations and informed decision-making.

Key Responsibilities:

• Ensure data accuracy and quality through defined standards, audits, and clean-up
• Manage data collection, validation, entry, updates, backups, and integration
• Use tools like Excel, Power Query, Power BI, Access, or SQL for data management and analysis
• Generate and validate reports, dashboards, and trend analyses to support decision making
• Collaborate with teams (e.g., Sales, Marketing, Finance) to meet data and reporting needs

Qualifications:

• Bachelor's degree in Data Management, Information Systems, Computer Science, Statistics, or a related field
• 2+ years of experience in data management or analytics
• Proficiency in tools such as Excel, Power BI & Access
• Strong attention to detail, data accuracy, and process discipline
• Excellent analytical, organizational, and communication skills

Preferred Skills:

• Experience working with SharePoint or OneDrive-based data sources
• Familiarity with Power Automate, Power Apps, or other workflow automation tools
• Ability to consolidate and transform large volumes of Excel-based data
• Familiarity with data visualization and business intelligence tools
• Basic Programming is a plus

Join our innovative team to shape the future of data governance in Consumer & Community Banking. Unlock your potential by driving compliance and oversight in AI/ML technologies. Be at the heart of delivering customer-centric products and services.

Job Summary:

As a Data Management Lead within the Consumer & Community Banking (CCB) Data Use Council & AI/ML Governance teams, you will coordinate with requesters and Control Partners from Controls, Legal, Compliance, and Risk to evaluate data use requests and present assessments to the firm's Chief Data and Analytics Officer (CDAO). You will identify legal, contractual, operational, and reputational risks, focusing on AI/ML and emerging technologies. This role supports the CCB AI Governance Program Office, ensuring effective oversight of related Standards and Procedures.

Job Responsibilities:

• Build and manage a team responsible for supporting the Data Use Council, setting direction and acting as an escalation point for issues.
• Oversee AI/ML use cases for compliance, establishing robust governance structures.
• Collaborate with CDAO and stakeholders to implement monitoring systems and assess risks.
• Demonstrate leadership and communication skills, with a background in governance and controls.
• Prioritize AI data use requests against product roadmaps, key deadlines, project go-live dates, and risk assessments.
• Coordinate review with key stakeholders and senior management, presenting AI data request overviews and risks.
• Work with internal clients (Digital, Marketing, Consumer Banking, Modeling, and management) to evaluate data use requests and identify necessary business requirements, guardrails, conditions, or controls.
• Establish AI communication and documentation team practices, including governance procedures, business informational sites, and workflows.
• Establish enhanced AI Metric Reporting and Oversight, supporting quality control reviews.
• Partner with Control Management to implement enhanced GenAI Use Case monitoring.

Required Qualifications, Capabilities, and Skills:

• Experience building and managing high-performing teams.
• Strategic thinking and planning skills, with abilities to drive innovation.
• Highly developed analytical skills and excellent attention to detail.
• Ability to communicate ideas effectively, both orally and written, to employees and executives.
• Ability to meet deadlines and handle multiple priorities and projects effectively.
• Quality-focused work ethic, effectively responding to rapidly changing business needs.
• Proactive self-starter with leadership and interpersonal skills.

Preferred Qualifications, Capabilities, and Skills:

• Bachelor's degree in business, legal, decision science, data management, or related field with 5-7 years' experience in those fields.
• Experience with technical concepts and working with technical staff as needed.
• Knowledge of PII, metadata, and other data management concepts.
• Proficiency in Microsoft Word, Excel, PowerPoint, Outlook, Visio, SharePoint.
• Prior experience with Data Governance, Estimation/Modeling Development, Legal, Compliance, Privacy, Risk, Controls, or Audit

The candidate should have minimum 2 years of experience in Meter Data Management.

Shift Schedule: 12PM to 10PM.

Work Set up: Hybrid. Number of days in a month or week that needs to be in the office: 2x per week office day.

Project Location (During onsite): CG2, Boni Mandaluyong.

Join our team as a Data Management Associate (for Data Entry) You'll be responsible for data entry from online documents to our prescribed system, identifying key components essential for completion, and maintaining effective email communication for processing and follow-ups.

Salary:

• Php 12,000 (this excludes perfect attendance bonus of Php1,000.00, night differentials, potential account specific incentives, etc)

Perks:

• Free daily meals
• Wellness programs
• Paid time off
• Continuous professional development
• Office location: KSS Building Buhangin and Aeon Towers, Bajada, Davao City

Key Responsibilities:

• Data entry from online documents to prescribed system
• Identify key components essential for data entry completion
• Completion within the prescribed period of time
• Email communication on processing and follow-ups

Work Schedule:

• Graveyard Shift

Ideal Candidate:

• Detail-oriented with strong data entry skills
• Excellent email communication skills
• Able to work independently and meet deadlines
• Comfortable working in a graveyard shift

Job Type: Full-time

Pay: From Php12,000.00 per month

Work Location: In person

Expected Start Date: 09/15/2025