Clinical Research Studies SME - Part-Time
4 days ago
Silver Spring
Overview DRT Strategies delivers expert management consulting and information technology (IT) solutions to large federal agencies the U.S. Navy state and local government and commercial clients in health care technology andfinancial services industries. The three letters of our name DRT stand for Driving Resolution Together which is the core philosophy on which the company was founded. That is we collaborate with our clients to solve their most pressing challenges - together. We are problem solvers dedicated to your success combining Fortune 500 experience with small business responsiveness. We have established a reputation with our clients as a forward-thinking consulting firm with demonstrated success in implementing solutions that lead to meaningful results. Our world-class consultants unite people to work collaboratively to achieve project goals and make vision a reality. Project Description: The project supports applied regulatory science research and operational activities for the FDA Center for Drug Evaluation and Research (CDER). The outcomes of divisional research will be used to inform drug development and regulatory evaluation that supports the FDAs mission to ensure that safe and effective drugs and biologics are available to the American people. Job Summary: The Clinical Research Studies SME will provide administrative support for applied regulatory science research and operational activities in addition the SME will provide specialized expertise to improve business and knowledge management processes as well as other operational procedures. Responsibilities: • Provide SME support to clinical research studies via the following activities-, • Develop study budget estimates., • Draft and/or review all required documentation: study protocol informed consent form statistical analysis plan study specific SOPs (e.g. safety management plans) concept paper final report., • Support development and submission of study manuscripts., • Support drafting of manuscript and supplemental materials prepare figures and tables as needed assist with journal submission and post-submission edits including responding to editor comments., • Assist the project team to develop overall study tracking and management support by creating tools like trackers activity checklists and a SharePoint PowerBI dashboard., • Capture processes in Manual of Procedures (MOP) document., • Create a clinical team subsite to capture and provide easy access to all resources., • Assist with overall project support as needed.Require Experience:, • Demonstrate having the necessary skills and experience to manage and conduct complex and diverse research/development projects including pharmacokinetic study of oral nasal and topical drug products to support FDAs requirement., • At least 3 years of experience with toxicology studies.Preferred Experience:, • Experience serving as a clinical study manager., • Experience working in research setting leading to regulatory submissions for the FDA., • Experience preparing drug applications in the pharmaceutical industry., • Familiarity with FDA regulatory process., • 5 years of experience working in research or regulatory setting., • Hands on experience working in a CRO., • Familiarity with SharePoint and EndNote, • Familiarity with Section 508 complianceEducation & Training:, • Masters degree (PhD preferred) in biomedical sciences.Salary Range:, • $43-58/hr EEO Commitment DRT Strategies Inc. (DRT) celebrates diversity and is proud to provide Equal Employment Opportunities (EEO) to all employees and qualified applicants for employment without regard to race color creed religion national origin gender sexual orientation age gender identity genetic information disability protected veteran status or any other protected characteristic under federal state or local laws. Reasonable accommodation for applicants and employees with disabilities will be provided. If a reasonable accommodation is needed to participate in the job application or interview process to perform essential job functions and/or to receive other benefits and privileges of employment please contact Human Resources by emailing ___Reasonable accommodation for applicants and employees with disabilities will be provided. If a reasonable accommodation is needed to participate in the job application or interview process to perform essential job functions and/or to receive other benefits and privileges of employment please contact Human Resources by emailing ___ ___Overview DRT Strategies delivers expert management consulting and information technology (IT) solutions to large federal agencies the U.S. Navy state and local government and commercial clients in health care technology andfinancial services industries. The three letters of our name DRT stand for Driving Resolution Together which is the core philosophy on which the company was founded. That is we collaborate with our clients to solve their most pressing challenges - together. We are problem solvers dedicated to your success combining Fortune 500 experience with small business responsiveness. We have established a reputation with our clients as a forward-thinking consulting firm with demonstrated success in implementing solutions that lead to meaningful results. Our world-class consultants unite people to work collaboratively to achieve project goals and make vision a reality. Project Description: The project supports applied regulatory science research and operational activities for the FDA Center for Drug Evaluation and Research (CDER). The outcomes of divisional research will be used to inform drug development and regulatory evaluation that supports the FDAs mission to ensure that safe and effective drugs and biologics are available to the American people. Job Summary: The Clinical Research Studies SME will provide administrative support for applied regulatory science research and operational activities in addition the SME will provide specialized expertise to improve business and knowledge management processes as well as other operational procedures. Responsibilities: • Provide SME support to clinical research studies via the following activities-, • Develop study budget estimates., • Draft and/or review all required documentation: study protocol informed consent form statistical analysis plan study specific SOPs (e.g. safety management plans) concept paper final report., • Support development and submission of study manuscripts., • Support drafting of manuscript and supplemental materials prepare figures and tables as needed assist with journal submission and post-submission edits including responding to editor comments., • Assist the project team to develop overall study tracking and management support by creating tools like trackers activity checklists and a SharePoint PowerBI dashboard., • Capture processes in Manual of Procedures (MOP) document., • Create a clinical team subsite to capture and provide easy access to all resources., • Assist with overall project support as needed.Require Experience:, • Demonstrate having the necessary skills and experience to manage and conduct complex and diverse research/development projects including pharmacokinetic study of oral nasal and topical drug products to support FDAs requirement., • At least 3 years of experience with toxicology studies.Preferred Experience:, • Experience serving as a clinical study manager., • Experience working in research setting leading to regulatory submissions for the FDA., • Experience preparing drug applications in the pharmaceutical industry., • Familiarity with FDA regulatory process., • 5 years of experience working in research or regulatory setting., • Hands on experience working in a CRO., • Familiarity with SharePoint and EndNote, • Familiarity with Section 508 complianceEducation & Training:, • Masters degree (PhD preferred) in biomedical sciences.Salary Range:, • $43-58/hr EEO Commitment DRT Strategies Inc. (DRT) celebrates diversity and is proud to provide Equal Employment Opportunities (EEO) to all employees and qualified applicants for employment without regard to race color creed religion national origin gender sexual orientation age gender identity genetic information disability protected veteran status or any other protected characteristic under federal state or local laws. Reasonable accommodation for applicants and employees with disabilities will be provided. If a reasonable accommodation is needed to participate in the job application or interview process to perform essential job functions and/or to receive other benefits and privileges of employment please contact Human Resources by emailing ___Overview DRT Strategies delivers expert management consulting and information technology (IT) solutions to large federal agencies the U.S. Navy state and local government and commercial clients in health care technology andfinancial services industries. The three letters of our name DRT stand for Driving Resolution Together which is the core philosophy on which the company was founded. That is we collaborate with our clients to solve their most pressing challenges - together. We are problem solvers dedicated to your success combining Fortune 500 experience with small business responsiveness. We have established a reputation with our clients as a forward-thinking consulting firm with demonstrated success in implementing solutions that lead to meaningful results. Our world-class consultants unite people to work collaboratively to achieve project goals and make vision a reality. Project Description: The project supports applied regulatory science research and operational activities for the FDA Center for Drug Evaluation and Research (CDER). The outcomes of divisional research will be used to inform drug development and regulatory evaluation that supports the FDAs mission to ensure that safe and effective drugs and biologics are available to the American people. Job Summary: The Clinical Research Studies SME will provide administrative support for applied regulatory science research and operational activities in addition the SME will provide specialized expertise to improve business and knowledge management processes as well as other operational procedures. Responsibilities: • Provide SME support to clinical research studies via the following activities-, • Develop study budget estimates., • Draft and/or review all required documentation: study protocol informed consent form statistical analysis plan study specific SOPs (e.g. safety management plans) concept paper final report., • Support development and submission of study manuscripts., • Support drafting of manuscript and supplemental materials prepare figures and tables as needed assist with journal submission and post-submission edits including responding to editor comments., • Assist the project team to develop overall study tracking and management support by creating tools like trackers activity checklists and a SharePoint PowerBI dashboard., • Capture processes in Manual of Procedures (MOP) document., • Create a clinical team subsite to capture and provide easy access to all resources., • Assist with overall project support as needed.Require Experience:, • Demonstrate having the necessary skills and experience to manage and conduct complex and diverse research/development projects including pharmacokinetic study of oral nasal and topical drug products to support FDAs requirement., • At least 3 years of experience with toxicology studies.Preferred Experience:, • Experience serving as a clinical study manager., • Experience working in research setting leading to regulatory submissions for the FDA., • Experience preparing drug applications in the pharmaceutical industry., • Familiarity with FDA regulatory process., • 5 years of experience working in research or regulatory setting., • Hands on experience working in a CRO., • Familiarity with SharePoint and EndNote, • Familiarity with Section 508 complianceEducation & Training:, • Masters degree (PhD preferred) in biomedical sciences.Salary Range:, • $43-58/hr EEO Commitment DRT Strategies Inc. (DRT) celebrates diversity and is proud to provide Equal Employment Opportunities (EEO) to all employees and qualified applicants for employment without regard to race color creed religion national origin gender sexual orientation age gender identity genetic information disability protected veteran status or any other protected characteristic under federal state or local laws. Reasonable accommodation for applicants and employees with disabilities will be provided. If a reasonable accommodation is needed to participate in the job application or interview process to perform essential job functions and/or to receive other benefits and privileges of employment please contact Human Resources by emailing