Title: Pathology Technologist - Chemistry and Hematology Location: New York United States Job Description: Job Description: Performs clinical laboratory procedures, examinations and other tests pursuant to established protocols including maintaining equipment and records and performing quality assurance activities related to examination performance requiring the exercise of independent judgment and responsibility. Job Responsibility: - Sets-up and performs a variety of routine and/or complex laboratory tests and procedures relevant to the particular lab area and personal qualifications. - Prepares and tests specimens for examination and reports results. - Follows established in-process quality control procedures including recording data. - Performs routine and/or preventive maintenance on laboratory equipment. - Troubleshoots basic instrumentation, culture media, chemicals, reagents, stains, solutions, technical problems and methodologies. - Maintains sufficient supplies at workstation. - Ensures and maintains quality control and assurance activities. - Uses Infection Control practices and procedures. 9.Performs related duties, as required. - ADA Essential Functions Job Qualification: - Bachelor's Degree in Medical Technology, Basic Science or related field, required. - Licensed by New York State Education Department (NYSED) as a Clinical Laboratory Technologist (or as appropriate to area of assignment) (LIC-CLT or LIC-CYTOT), required. - Minimum of one (1) year work experience and/or training specific to the work being done in the area noted above, required. - Experience working in Chemistry & Hematology strongly preferred. Work Schedule: Part Time - Three nights per week / Two weekdays & Alternating Weekends - Additional Salary Detail The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).

• Responsible for developing and implementing UK regulatory strategies for product(s). • Lead the UK RA team to manage regulatory aspects of compounds. • Collaborate with key internal stakeholders on UK MAA strategy. • Manage the content and prepare regulatory (UK MAA) dossiers. • Oversee communications, submissions, and approvals from regulatory agencies. • Act as the RA liaison within the UK Leadership team and provide input into UK business strategy. • Anticipate and mitigate regulatory risks while maintaining knowledge of regulatory intelligence. • Mentoring junior team members and representing BeOne at UK industrial meetings.

Role Description Remote Recruitment is hiring a Compliance Officer to ensure a UK-based business operates within regulatory and legal frameworks. Working fully remotely from South Africa, you'll maintain compliance programmes, conduct reviews, and advise the business on regulatory matters. - Monitor regulatory developments and assess their impact on business operations - Maintain and update compliance policies, procedures, and frameworks - Conduct internal compliance audits and risk assessments - Provide compliance training and guidance to staff across the business - Liaise with regulators and manage regulatory reporting obligations Qualifications - 4+ years of compliance experience, ideally in financial services or a regulated UK industry - Strong knowledge of UK regulatory frameworks and compliance requirements - Excellent analytical skills and attention to detail - Clear and concise written and verbal communication skills - Reliable internet and a professional home workspace Benefits - Salary: R32,000 per month - Full-time, permanent remote position - Working hours: 09:00–17:00 UK time (11:00–19:00 SAST) - Equipment provided - 20 days paid leave Company Description We welcome all applicants. Apply today to play a critical role in a UK-regulated business.

• Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks. • Responsible for driving country level submissions and site activation processes by coordinating activities when multiple RSSs are assigned within the country. • Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to CA, EC and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH-GCP. • Interaction with CA/EC for study purposes and handling responses to the CA/EC. • Providing regular updates about CA and EC submissions to the Start Up Lead and/or Regulatory Lead assigned to the study and to Project Manager/Project Team as relevant. • Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership updated. • Preparation/Support the development of study specific start-up plans, IMP release requirements and essential document review criteria. • Partner with the assigned site CRA to ensure alignment in communication and secure site collaboration. • Prepare, review and manage collection of essential documents required for site activation/IMP release. • Customize country/site specific Patient Information Sheet and Informed Consent Forms. • Responsible for/facilitates the translation and co-ordination of translations for documents required for submission. • Maintain communication with other key functions participating to country start up i.e., Feasibility, Clinical Operations, Project Management, Regulatory, and Site Contracts management group on project specific status and deliverables. • Act as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent Authority, local IRB/Ethics Committee (EC) timelines, site contracts and budget negotiation requirements and other required reviews to secure on time site activation for the assigned sites in the country. • When required, participate/support the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee department. • Keep an updated knowledge of the local clinical trial laws, regulations and help distributing this knowledge within PfM to ensure the conduct of Clinical Trials according to international and local/national applicable regulations. • Maintain audit/inspection readiness at all times and file documents as per TMF plan and/ or study specific plans in the relevant TMF. • May support the clinical team performing Pre-Study Site Visits. • May participate/support feasibility group in site outreach to assess potential interest of investigators to a potential study. • Will support development of country specific Country Start-up summary and process flow identifying timelines, risks, and success factors. • Will support development of training sessions to expand Country Start-up knowledge and act as Subject Matter Expert for queries. • Will mentor staff on local country regulations, submissions and internal procedures, as well as on PFM SSU specific guidance and tools. • Can assume ownership of departmental process improvements / initiatives, including finalization, roll out and periodic reviews. • May interact with clients to provide activation readiness status updates, request documents or document review, and participate in proposal activities, including slide development and client presentation as required.