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 management 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.

Adelphi is seeking a Physician to provide clinical consulting services in a school setting located in Austin, Texas. The ideal candidate will partner with school health leadership to deliver expert medical guidance, oversight, and policy support to ensure safe, compliant, and high-quality student health services. Job Quick Facts: • BD-1317-23 • Profession: Physician • Specialty: Pediatrics, Family Medicine, or Adolescent Medicine • Location: Austin, Texas • Facility Type: School • Job Type: Part-Time • Shift Schedule: Up to 4 hours per month (flexible; virtual or onsite) • Rate: $115-$125 Requirements: • Medical Degree (MD or DO) from an accredited institution • Active, unrestricted Texas medical license • Board certification in Pediatrics, Family Medicine, or Adolescent Medicine • No current disciplinary actions impacting practice • Experience working with pediatric/adolescent populations preferred • Knowledge of school health regulations, public health guidance, and compliance standards Responsibilities: • Provide clinical oversight and expert consultation on student health services across K–12 settings • Advise school health staff on management of chronic conditions (e.g., asthma, diabetes, seizures, behavioral health) • Interpret and apply public health guidance (e.g., CDC, AAP) for school operations and communicable disease response • Support development and review of health policies, protocols, and standing orders to ensure legal and regulatory compliance • Provide consultation on complex student health cases and clarify scope-of-practice for school health staff • Guide emergency preparedness and response planning (e.g., anaphylaxis, seizures, asthma events, infectious disease outbreaks) • Collaborate with interdisciplinary teams (school nurses, administration, special education, and wellness leadership) to support decision-making • Advise on risk management, documentation practices, and liability mitigation related to student health services • Promote population health strategies and health equity initiatives for student communities • Assist in communicating complex medical information to staff, students, and families • Maintain availability for timely consultation and scheduled meetings • Any other duties as assigned

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 expereince 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.