The Collections Organization is seeking a Collections Analyst who will contribute to the achievement of the company’s financial goals. The ideal candidate will thrive as a collaborative member of a dynamic and close-knit team, bringing a proactive and flexible approach to their work. The individual should possess the ability to adapt to an evolving work environment where assignments and priorities may shift frequently. This position offers competitive compensation and fosters career opportunities for employees looking to further their professional growth. This position is 100% remote nationwide. Typical Responsibilities: - Manage invoice and project collections, executing individual plans to maximize revenue for the company. - Effectively multi-task while maintaining high attention to detail in a fast-paced environment with minimal supervision. - Work independently and collaboratively as part of a team, demonstrating a strong commitment to meeting the company’s financial goals and objectives. SAIC® is a premier Fortune 500® mission integrator focused on advancing the power of technology and innovation to serve and protect our world. Our robust portfolio of offerings across the defense, space, civilian and intelligence markets includes secure high-end solutions in mission IT, enterprise IT, engineering services and professional services. We integrate emerging technology, rapidly and securely, into mission critical operations that modernize and enable critical national imperatives. We are approximately 24,000 strong; driven by mission, united by purpose, and inspired by opportunities. SAIC is an Equal Opportunity Employer. Headquartered in Reston, Virginia, SAIC has annual revenues of approximately $7.5 billion. For more information, visit saic.com. For ongoing news, please visit our newsroom.

SAIC has an opening for an Accounting Associate position within the Billing department. This is an excellent opportunity to gain exposure to bill advanced contracts within Costpoint, provide analysis required for the contracts and to interact with various other areas within FSS. This position will be responsible for validating project setup activities to ensure accurate billing of the contracts, meeting all billing requirements for the contracts including meeting the project due dates and deadlines, and working closely with the Program Teams to ensure seamless billing. The responsibilities encompass maintaining accurate billing instructions and funding documentation for assigned projects. The selected candidate will be responsible for billing a wide variety of projects and perform other departmental duties such as GSA entries, Payment Reconciliations, Training, and various ad hoc duties. This includes understanding, interpreting, and analyzing intermediate level to gather requirements to accurately bill and submit invoices. For the right candidate, this position can be performed remotely from any location within the United States. Typical Responsibilities: - Financial contract review - Evaluate and perform accurate contract billing - Provide information to other functional areas to assist in the effectiveness of billing - Create and maintain less complex to intermediate project billing - Provide customer service to other functional areas SAIC® is a premier Fortune 500® mission integrator focused on advancing the power of technology and innovation to serve and protect our world. Our robust portfolio of offerings across the defense, space, civilian and intelligence markets includes secure high-end solutions in mission IT, enterprise IT, engineering services and professional services. We integrate emerging technology, rapidly and securely, into mission critical operations that modernize and enable critical national imperatives. We are approximately 24,000 strong; driven by mission, united by purpose, and inspired by opportunities. SAIC is an Equal Opportunity Employer. Headquartered in Reston, Virginia, SAIC has annual revenues of approximately $7.5 billion. For more information, visit saic.com. For ongoing news, please visit our newsroom.

Role Description Precision for Medicine are recruiting a Regulatory Manager / Senior Regulatory Manager (depending on experience) to join our team. The Regulatory Manager provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely preparation of well organized, quality regulatory submissions in compliance with applicable regulations. The Regulatory Manager coordinates and prepares regulatory documents for submission to Regulatory Authorities and/or Ethics Committees, as applicable. - Provides regulatory guidance throughout the clinical development life cycle - Compile, coordinate and review applications to Regulatory Authorities including, but not limited to, CTA/IND, annual reports, routine amendments, scientific advice/regulatory authority meetings, orphan designations, paediatric planning, and marketing applications. Also provides strategic regulatory input as required - Develops and/or reviews documents intended for submission to the Regulatory Authorities and/or Ethics Committees to assure compliance with regulatory standards - Serve as representative of Global Regulatory Affairs at project team meetings with both external and internal customers - Works within a project team, and where necessary, leads project for the region or globally - Oversee and coordinate Regulatory Affairs Specialists to achieve submission targets for contracted programs - Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership updated - Assist in development of Regulatory Affairs Specialists and other operational area staff, as required - Provide input, as required, into regulatory strategy and timeline development for new study opportunities - Assists in establishing company standards to ensure the highest quality of submitted information - Participates in maintaining and executing on the corporate quality initiatives across business units within clinical solutions - Keeps abreast and continually expand knowledge of laws, regulations and guidelines governing drug development and approval - Provides ICH GCP guidance, advice and training to internal and external clients - Serve as representative of Global Regulatory Affairs at business development meetings Qualifications - Minimum Required: - Bachelors degree, or equivalent experience, ideally in a scientific or healthcare discipline - 5 years Regulatory experience required for the Manager level and 7 years Regulatory experience required for the Senior Manager Regulatory level - Computer literacy (MS Office/ Office 365) - Fluent in English - Preferred: - Graduate, postgraduate - Possesses basic understanding of financial management - Other Required: - Candidates must have regulatory affairs experience working for a Clinical Research Organisation and have experience leading Clinical Submissions - Informed knowledge of all aspects of the drug development process inclusive of regulatory milestones and specialized knowledge of regulatory activities for at least one major region (EU, US) including but not limited to submissions to Regulatory Authorities, including INDs/CTAs and amendments, Scientific Advice Procedures, and post-approval submissions - Ability to understand clinical and pre-clinical study results, to help in its interpretation for regulatory positions and strategy - Knowledgeable of clinical trials methodology, including a working knowledge of protocols and indications being studied - Knowledge and expertise with relevant regulations and guidance supporting pharmaceutical development - Availability for domestic and international travel including overnight stays Requirements - Strong interpersonal skills and a proven ability to contribute to a team environment involving balancing the demands stemming from multifaceted research activities - Demonstrates an acceptable degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates - Ability to manage multiple and varied tasks in a fast-moving environment, good record-keeping skills - Exhibits high self-motivation, and is able to work and plan independently as well as in a team environment - Motivates other members of the project team to meet timelines and project goals - Flexible attitude with respect to work assignments, and new learning - Resolves project related problems and prioritize workload to meet deadlines with little support from management - Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective - Collects data of consistently high standard - Communicates effectively in the English language both verbally and in written form - Conducts formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency Benefits - We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. - We strive to ensure employees feel appreciated for the contributions they make every single day. - You will provide input and have your ideas valued and nurtured, impacting positive change for the company.

• Preparation and coordination of monthly, quarterly and annual financial statements • Preparation and review of journal entries, provisions, accruals and account reconciliations • Application and ensuring compliance with US GAAP • Support for statutory financial statement preparation under HGB (or other European accounting standards) • Liaison with internal and external auditors and support during audits • Identification and implementation of process improvements in the accounting area • Participation in finance projects and the further development of systems and processes