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.

Job Title: Part-Time Periodontist Location: Eagles Landing and Vinings, GA Schedule: Part-Time | 2 days per week Why This Opportunity Stands Out Imagix, in partnership with Dental One Associates, is seeking a skilled and experienced Part-Time Periodontist to support specialty care across our established practices in Eagles Landing and Vinings, GA. This opportunity allows you to deliver high-quality periodontal care in a patient-centered, professionally run environment with consistent referral flow and strong clinical support. The role is structured as 2 days per week, providing predictable specialty coverage and the ability to focus on clinical excellence. About Us Imagix and Dental One Associates are committed to redefining the dental experience through advanced technology, collaboration, and a strong focus on patient care. Our practices support specialists with experienced teams, modern facilities, and established referral networks that allow providers to focus on outcomes and long-term success. What We Offer - Strong internal patient referral system - Earning Potential: $2500 - $3500 per day - Full clinical autonomy to diagnose and treat patients - Patient-care–centric practice culture - Modern facilities, periodontal equipment, and technology - Established clinical and administrative support - Continuing education and professional development support - 401(k) participation (where applicable) The Role - Provide comprehensive periodontal specialty care - Diagnose and treat periodontal disease and conditions affecting the supporting structures of teeth - Perform surgical and non-surgical periodontal procedures - Develop and present treatment plans based on clinical examinations and diagnostic findings - Educate patients on periodontal health, treatment options, and long-term maintenance - Collaborate closely with referring dentists and in-office clinical teams - Maintain the highest standards of ethics, professionalism, and clinical excellence - Remain current with evolving technologies and standards of care through continuing education Qualifications - DDS/DMD from an accredited dental school - Specialty certificate from an accredited residency program in Periodontist - Active dental license in the state of practice - Commitment to high-quality patient care and professional ethics - Strong communication and interpersonal skills to build trust and long-term patient relationships Legal Disclaimer: Wecomply withall minimum wage laws as applicable. All benefits are subject to potential vesting and eligibility requirements. The company is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, ancestry, color, age, national origin, ethnicity, religious creed or belief, physical or mental disability, marital or familial status, legally protected medical condition, genetic information, military or veteran status, sex, gender, sexual orientation, citizenship status, or any other characteristic protected by applicable law.