Associate Scientist - Immunochemistry

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting Job Description This is a fully onsite role based at our BioAnalytical in Richmond, VA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.   Must be legally authorized to work in the United States without sponsorship.  Must be able to pass a comprehensive background check, which includes a drug screening.  The working shift for this role is Monday - Friday ~8AM-5PM. Join us as an Associate Scientist! At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. As an Associate Scientist your role will be to oversee the operations of clinical laboratory testing, ensure the accuracy and reliability of results, manage and mentor lab staff, and uphold the highest standards of quality and compliance in all laboratory practices. What You’ll Do: • Perform lab work in accordance with client protocols, methods and requirements. • Prepare study protocols, project status reports, final study reports and other project-related technical documentation. • Design experimental study and participates in technical troubleshooting. • Review, interpret and analyze data for technical quality and compliance to protocols, methods and SOPs. Review laboratory investigations and deviation. • Organize, schedule and supervise laboratory resources for group's project activities and updates project status. • Respond to client questions and needs, coordinate client communication and records meeting minutes. • Assist group leaders in their responsibilities. • Assist in preparation and implementation of PPD/client SOPs and company operational policies. Ensure adherence to SOPs, safety standards and company policies. Education and Experience: • Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 to 2 years). In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: • Knowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines • Knowledge of applicable regulatory authority, compendia and ICH guidelines • Excellent manual dexterity skills • Good written and oral communication skills • Time management and project management skills • Proven problem solving and troubleshooting abilities • Ability to cross-train on sample preparation techniques with another laboratory group • Ability to work in a collaborative work environment with a team Working Conditions