Role Description A Sommelier promotes and provides an excellent wine service to our guests. Improves and maintains wine sales. Responsibilities - Provides wine service to guests in the restaurant and buffet restaurant. In some cases will be responsible for providing bar services other than wine. - Works in a station designated by the Head Sommelier and approved by the Restaurant Manager and follows the daily schedule, which is posted weekly in the wine cellar. - In addition to serving wine, duties include the re-stocking of the wine cellar on a daily basis, and once a week may be requested to work during the loading of wines onto the ship. - Ensures personal appearance, personal hygiene and uniform appearance are at all times in accordance with the company policy. - Should be knowledgeable about the wine list and able to discuss and suggest wines to guests who ask for advice. The knowledge of how to pair wine with food is imperative. - Has a clear understanding of the company's service standards. - Applies salesmanship techniques in order to achieve maximum sales, which will result in higher personal compensation. - Must be able to reach reasonable and attainable sales targets set by the company. This requires self-confidence and commitment to the sales goals. - Reports all guests' queries, discrepancies or suggestions to his/her immediate supervisor. Must have full knowledge of the cashless system on board the ship in order to process all transactions accordingly. - Duties include the cleaning and sanitizing of his/her working area and working utensils following the United States Public Health rules and regulations at all times. Qualifications - Minimum of five years beverage-related experience (shipboard experience preferred), or an equivalent combination of experience and education. - Completion of high school or basic education equivalency required. - Advanced level of English. - 21+ years old. Benefits - Free food & accommodation (2 people per cabin). - Perfect chance to travel the world. - Work in Royal Caribbean Cruises Ltd. named one of the Top-Rated Workplaces. - Enjoy activities for crew (gym, social activities, crew events, etc). - Earn recognition and career advancement opportunities. - Experience working with more than 72 nationalities. - Permanent job with contract 6-8 months onboard followed by 60 days of vacation. - Save Money as you do not pay for food and accommodation on board. - Competitive salary (find out when apply). - Visa fee will be reimbursed on board. - Medical insurance provided during contract.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Data Assoc II – 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 expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Assoc II, you will perform advanced aspects of the data cleaning process with a high level of accuracy and in accordance with Good Clinical Practices (GCPs) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs), to assess the safety and efficacy of investigational products and/or medical devices. What You’ll Do: • Identify, resolve, and update data discrepancies. Make changes to the data management database as required. • Generate, track and resolve data clarifications and queries. May implement CRF design in identified graphic design package. • Review data listings for accuracy and consistency of data. Analyze and resolve data validation and other data management reports. • Produce project-specific status reports for CDM management and for clients on a regular basis. • Perform data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews. Education and Experience Requirements: • Any Life Science Graduate • Technical positions may require a certificate • 4-6 Years of experience in Clinical Data Manager Role Having Experience in Veeva EDC is preferred. Knowledge, Skills and Abilities: • Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations • Strong attention to detail and skill with numbers and ability to use interactive computer programs • Good written and verbal communication skills and a strong command of English language and grammar • Good organizational and analytical/problem-solving skills • Ability to work productively with moderate supervision • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data • Strong customer focus and excellent interpersonal skills. • Proven flexibility, adaptability and ability to work in a team environment or independently as needed • Must demonstrate good judgment in making decisions • Knowledge of medical/clinical trial terminology • Understands project protocol and Data Validation Manual Working Conditions and Environment: • Work is performed in an office or clinical environment with exposure to electrical office equipment. • Occasional drives to site locations. Potential Occasional travel required. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Data Assoc II – 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 expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Assoc II, you will perform advanced aspects of the data cleaning process with a high level of accuracy and in accordance with Good Clinical Practices (GCPs) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs), to assess the safety and efficacy of investigational products and/or medical devices. What You’ll Do: • Identify, resolve, and update data discrepancies. Make changes to the data management database as required. • Generate, track and resolve data clarifications and queries. May implement CRF design in identified graphic design package. • Review data listings for accuracy and consistency of data. Analyze and resolve data validation and other data management reports. • Produce project-specific status reports for CDM management and for clients on a regular basis. • Perform data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews. Education and Experience Requirements: • Any Life Science Graduate • Technical positions may require a certificate • 4-6 Years of experience in Clinical Data Manager Role Having Experience in Veeva EDC is preferred. Knowledge, Skills and Abilities: • Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations • Strong attention to detail and skill with numbers and ability to use interactive computer programs • Good written and verbal communication skills and a strong command of English language and grammar • Good organizational and analytical/problem-solving skills • Ability to work productively with moderate supervision • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data • Strong customer focus and excellent interpersonal skills. • Proven flexibility, adaptability and ability to work in a team environment or independently as needed • Must demonstrate good judgment in making decisions • Knowledge of medical/clinical trial terminology • Understands project protocol and Data Validation Manual Working Conditions and Environment: • Work is performed in an office or clinical environment with exposure to electrical office equipment. • Occasional drives to site locations. Potential Occasional travel required. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Data Assoc II – 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 expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Assoc II, you will perform advanced aspects of the data cleaning process with a high level of accuracy and in accordance with Good Clinical Practices (GCPs) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs), to assess the safety and efficacy of investigational products and/or medical devices. What You’ll Do: • Identify, resolve, and update data discrepancies. Make changes to the data management database as required. • Generate, track and resolve data clarifications and queries. May implement CRF design in identified graphic design package. • Review data listings for accuracy and consistency of data. Analyze and resolve data validation and other data management reports. • Produce project-specific status reports for CDM management and for clients on a regular basis. • Perform data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews. Education and Experience Requirements: - • Any life science graduate - Technical position may require a certificate - 4 - 6 Years of experience in clinical data manager role - Having Experience in Veeva EDC is preferred Knowledge, Skills and Abilities: • Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations • Strong attention to detail and skill with numbers and ability to use interactive computer programs • Good written and verbal communication skills and a strong command of English language and grammar • Good organizational and analytical/problem-solving skills • Ability to work productively with moderate supervision • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data • Strong customer focus and excellent interpersonal skills. • Proven flexibility, adaptability and ability to work in a team environment or independently as needed • Must demonstrate good judgment in making decisions • Knowledge of medical/clinical trial terminology • Understands project protocol and Data Validation Manual Working Conditions and Environment: • Work is performed in an office or clinical environment with exposure to electrical office equipment. • Occasional drives to site locations. Potential Occasional travel required. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs.