• To provide expert statistical input to Phase I-IV global clinical trials, including the design of clinical trials (protocol, sample size, randomisation, etc) and the production and review of analysis and reporting deliverables (including statistical analysis plans) on behalf of and/or in conjunction with Aixial Group clients. • Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for global Phase I-IV trials. • Statistical programming and QC of tables, listings and figures for global Phase I-IV trials. • Responsible for the quality and timeliness of statistical deliverables. • As lead Statistician, to be primarily responsible for all statistical activities on allocated studies including planning and coordination of activities for assigned statistical team members.

Salary: PHP 40,000- PHP 60,000/ month Job Description: - Track mandated school health screenings such as vision, hearing, and scoliosis screenings, and ensure outcomes are properly documented. - Monitor student immunization compliance and assist in managing exclusion notices in accordance with state regulations. - Prepare and submit required public health reports, including communicable disease and outbreak reporting. - Coordinate with parents, teachers, school staff, and external healthcare providers to ensure continuity of care for students. - Analyze health office utilization data, including injuries, chronic condition management, and absenteeism trends. - Identify patterns and provide insights that can support preventive health strategies within schools. Minimum Qualifications: - Graduate of Bachelor of Science in Nursing. - Consultancy basis: Minimum of 6-month consultancy contract. - Registered Nurses (RN) and Non-Licensed Nurses are welcome to apply. - Registered Nurses: Must have at least 3 years of relevant nursing experience. - Non-Licensed Nurses: Must have at least 5 years of relevant healthcare or clinical support experience. - Strong organizational, documentation, and coordination skills. - Excellent written and verbal English communication skills. - Experience with health documentation, compliance tracking, or healthcare reporting is an advantage. - Willing to work night shift / graveyard shift to support US-based clients. - Must be able to work from home with a reliable internet connection. Others: - Equipment/ company computer is provided

JOB DESCRIPTION: Job Description Abbott’s Electrophysiology division is at the forefront of transforming cardiac care through cutting-edge technologies that diagnose and treat abnormal heart rhythms. With a fast-growing portfolio that includes advanced mapping systems, ablation catheters, and remote monitoring solutions, Abbott empowers clinicians to restore healthy heart function and improve patient outcomes. As part of our continued investment in team growth, we’re excited to introduce a new opportunity for a Clinical Team Leader to join Abbott’s Electrophysiology (EP) division, covering the South East UK region. The ideal candidate will be based in Central/Greater London) and play a key role in supporting our cutting-edge cardiac technologies in the field. Importantly, this position is a fantastic stepping stone into people management, making it an excellent fit for those aspiring to grow into future leadership roles within the organization. What you'll do: - Lead, coach and develop a team of Field technical Engineers within the region. - Drive continuous upskilling and refreshment of practice across the field team to support ongoing learning and development. - Equip the regional FTE team with the training and coaching needed to maximize product usage and upgrades where clinically appropriate. - Optimize product application to deliver the best possible patient outcomes, ensuring access to leading clinical technologies. - Ensure highest standards of clinical excellence in EP are maintained across our field team, including complex & non complex mapping, in lab solution creation, customer training and product differentiation. - Work within region, supporting the regional sales manager, to ensure alignment on key clinical activities and to ensure allocation of resource. - Build and maintain relationships with local Key Opinion Leaders (KOL’s) to encourage their continuous input on conventional therapies and technologies, emerging technologies and patient requirements. - Promote best in class patient outcomes. - Create a shared vision of how the teams’ activities align to EP team strategy. As part of a team driving innovation in one of MedTech’s fastest-growing markets, you’ll help shape the future of arrhythmia care and make a meaningful impact on lives around the world. What you'll need: - Relevant clinical experience in EP. - Scientific background. - Previous experience in 3D mapping. - Strong personal or group leadership skills. - Collaborative style, able to build and maintain strong relationships. As you would expect from an innovative global health care company, we offer a competitive range of benefits to support you and your family, including excellent salaries, bonus potential, a fantastic defined contribution pension scheme, private healthcare, life assurance and a flexible benefits scheme. We also offer fantastic development opportunities, including an established EP career pathway. The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted. JOB FAMILY: Support Services DIVISION: EP Electrophysiology LOCATION: United Kingdom > Solihull : Remote ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 75 % of the Time MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Driving a personal auto or company car or truck, or a powered piece of material handling equipment

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you’ll have the opportunity to provide administrative and technical support to the Project Team. As a Senior Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements. What You’ll Do: • According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. • Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. • Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate. • Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system. • Provides system support (i.e. GoBalto & eTMF). • Supports RBM activities. • Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members. • Supports scheduling and organization of client and/or internal meetings with completion of related meeting minutes. • Reviews and tracks local regulatory documents. • Transmits documents to client and centralized IRB/IEC. • Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation. • Maintains vendor trackers. • Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites. • Assists with study-specific translation materials and translation QC upon request. • May attend Kick off meeting and take notes when required. Education and Experience Requirements: • High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. • Bachelor's degree preferred. • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: • Ability to work in a team or independently as required • Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively • Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency • Strong customer focus • Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines • Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout • Excellent English language and grammar skills and proficient local language skills as needed • Good presentation skills • Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems • Ability to successfully complete PPD clinical training program • Self-motivated, positive attitude with effective strong interpersonal skills Working Conditions and Environment: • Work is performed in an office/ laboratory/clinical/ and/or home office environment with exposure to electrical office equipment. • Occasional drives to site locations. Potential Occasional travel required