• Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the clinical projects assigned. • Assist in the selection of sites, site evaluation visits, initiation visits and ensure follow-up by obtaining pre-study documentation to ensure good start-up of the investigation sites. • May act as Feasibility Associate. • Train site staff in all study procedures. • Conduct periodic monitoring visits, including completion of monitoring visit report. Review at each visit the accuracy, legibility, completeness and quality of the Case Report Forms (CRF). • Conduct source data verification and in-house review of clinical data and ensure timely resolution of data queries to guarantee reliable clinical data. • Manage the investigational products (storage, inventory, dispensing records, packaging and labelling) and the trial material (Investigator Study File (ISF), CRF, questionnaires, diaries, etc.) to ensure timely and correct supply to the site. • Cooperate with the site staff to ensure proper reporting from the site for safety issues (AEs, SAEs, SUSARs, etc.) and their follow-up, guaranteeing timely and appropriate handling of safety issues. • Conduct and report study termination and related activities (e.g. archiving) guaranteeing smooth completion of the project. • Act as the main contact person for the site to ensure close follow up. • Provide general support to the Clinical Research Division on quality control of clinical data. • Address appropriate team members about any issues that can jeopardize the conduct of the clinical projects assigned in a timely manner. • Report to the Head of department on all activities performed during the study and send all relevant documents according to the timelines and the requirements agreed for each single clinical trial. • Develop training material and give training in collaboration with the Training & Qualification Management Unit. • May assist with contract negotiation with sites on study budget after appropriate training. • Assist with the preparation of the study, including CRF design/development, write CRF instructions and organize the study files and documents to ensure good start-up of the investigation sites.

• Participate in the design and execution of global studies for regulatory submissions, reimbursement and product adoption, including clinical study documents (protocol, case report forms, etc.), study implementation and data management. • Manage study preparation, activation, enrollment, submission, maintenance and closure activities. • Participate in administrative activities associated with the clinical department including procedures, training of key personnel and preparation and maintenance of objectives and budgets. • Interface with representatives from key functional groups to drive product development within core teams, and clinical wide or cross-departmental initiatives. • Ensures appropriate oversight of clinical study by internal and external resources including, but not limited to monitoring staff, CROs and core laboratories. • Manage key study investigators; foster and maintain strong relationships through direct interactions with medical advisors and clinical leaders. • Negotiate contracts with hospitals, consultants, investigators, CROs, database management firms and outside suppliers. • Supervise training of investigators, site staff and field clinical staff. • Evaluates clinical and adverse event data during the conduct of the study and for completion of clinical study reports and other technical documents. • Ensures quality by maintaining compliance, reviewing device complaints, reviewing audit reports and implementing corrective actions. • Regularly communicates study status to senior management and represents organization to key customers.

• Participate in the design and execution of global studies for regulatory submissions, reimbursement and product adoption, including clinical study documents (protocol, case report forms, etc.), study implementation and data management. • Manage study preparation, activation, enrollment, submission, maintenance and closure activities. • Participate in administrative activities associated with the clinical department including procedures, training of key personnel and preparation and maintenance of objectives and budgets. • Interface with representatives from key functional groups to drive product development within core teams, and clinical wide or cross-departmental initiatives. • Ensures appropriate oversight of clinical study by internal and external resources including, but not limited to monitoring staff, CROs and core laboratories. • Manage key study investigators; foster and maintain strong relationships through direct interactions with medical advisors and clinical leaders. • Negotiate contracts with hospitals, consultants, investigators, CROs, database management firms and outside suppliers. • Supervise training of investigators, site staff and field clinical staff. • Evaluates clinical and adverse event data during the conduct of the study and for completion of clinical study reports and other technical documents. • Ensures quality by maintaining compliance, reviewing device complaints, reviewing audit reports and implementing corrective actions. • Regularly communicates study status to senior management and represents organization to key customers. • Other duties as assigned.

• Manage a small team of data analysts, supporting them in their deliverables and career development • Feedback on SEO data requests for feasibility, usability, and scalability • Feedback on methodologies from Methodology team for clarity, reliability and validity • Leverage a team of researchers to collect product and service data, with a focus on Health & Wellness and Home products • Oversee processes for quality control and data sanitization • Perform analysis on collected data to identify top-quality products and services • Collaborate with peers to introduce and develop new techniques and processes for efficient data collection • Work with the editorial team to establish priorities and maintain regular pipeline throughput • Review editorial content resulting from work product for accuracy and completeness