Role Description The TMF Document Coordinator I plays a key support role in maintaining the Sponsor’s Trial Master File (TMF) throughout the duration of a clinical trial. The TMF Coordinator I reviews and processes TMF records through quality control workflows to ensure they meet required quality, compliance, and regulatory standards before being approved into the TMF, following study-specific guidelines, SOPs, and ICH‑GCP requirements. - Review TMF records for completeness, accuracy, and quality prior to approval. - Classify records and assign appropriate metadata based on record type. - Identify quality issues, issue pre‑approval queries, and coordinate with submitters to ensure timely resolution. - Participate in TMF quality reviews and address assigned findings promptly. - Assist in maintaining study milestones and expected document lists. - Support the TMF Project Lead in generating monthly TMF metrics and related reports. - Attend internal TMF Focus meetings to provide updates on TMF status, issues, and outstanding queries. - Collaborate with project team members to resolve issues impacting TMF records. Qualifications - College degree. - Experience in clinical research within the biotechnology, pharmaceutical, or CRO industry. - Intermediate proficiency in English. - Computer skills and proficiency in Microsoft Word and Excel. - Good organizational skills with the ability to manage multiple assignments. - High attention to detail and accuracy. - Ability to meet established timelines, expectations, and objectives. - Adaptable and comfortable working in a multitasking environment. - Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines. Benefits - Flexible work schedule. - Permanent full-time position. - Ongoing learning and development. Company Description At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability, and responsiveness. We offer a stimulating work environment and attractive advancement opportunities. Indero is a Global Clinical Leader in Dermatology and Rheumatology. Formerly known as Innovaderm, Indero is a world-renowned expert and clinical research leader in dermatology with more than two decades of experience serving a broad range of indications, patient populations, administration routes, and drug classes, and a global footprint. Indero is a dual-focus CRO for dermatology and rheumatology, with 25+ years’ experience in clinical research and trial delivery. Our full-service approach provides biotech and pharmaceutical sponsors with the rigorous scientific foundation and tailored expertise their studies need to reach the finish line efficiently and effectively. Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. Indero only accepts applicants who can legally work in India.

At DraftKings, AI is becoming an integral part of both our present and future, powering how work gets done today, guiding smarter decisions, and sparking bold ideas. It's transforming how we enhance customer experiences, streamline operations, and unlock new possibilities. Our teams are energized by innovation and readily embrace emerging technology. We're not waiting for the future to arrive. We're shaping it, one bold step at a time. To those who see AI as a driver of progress, come build the future together. The Crown Is Yours As a Director, Regulatory Compliance, you'll play a critical role in safeguarding the integrity of DraftKings' prediction markets. You'll operate at the intersection of regulation, surveillance, and operations, helping ensure markets are fair, compliant, and built to scale. In this role, you'll work closely with internal stakeholders and external regulators to monitor trading activity, guide regulatory strategy, and strengthen market oversight. Your work will directly shape a trusted, future-ready exchange in a rapidly evolving regulatory landscape. What you'll do as a Director, Regulatory Compliance - Conduct daily T+1 trade practice surveillance to monitor market activity and support the onboarding of new customers. - Prepare, draft, and submit regulatory filings, including rule amendments and new product submissions, to the Commodity Futures Trading Commission with accuracy and timeliness. - Identify, investigate, and escalate potential violations of Exchange rules in alignment with regulatory requirements. - Partner closely with the Chief Regulatory Officer to manage investigations, address trade practice violations, and support regulatory reporting. - Step in to provide leadership and oversight for the Market Regulation function in the absence of the Chief Regulatory Officer. - Build and maintain strong relationships with internal teams and external regulators to support ongoing compliance with applicable rules and regulations. - Act as the primary liaison between the Exchange and third-party providers to implement and enhance market surveillance systems. What you'll bring - At least 10 years of progressive experience in market regulation or compliance within a Designated Contract Market, futures commission merchant, broker-dealer, or regulatory oversight organization. - Deep understanding of trade lifecycles, including order processing, clearing, settlement, and reconciliation. - Strong attention to detail with the ability to manage sensitive, time-critical data accurately and responsibly. - Ability to operate independently while managing complex regulatory and operational priorities. - Familiarity with case management systems and market surveillance tools. - Interest in prediction markets, sports trading, or broader financial markets. Join Our Team We're a publicly traded (NASDAQ: DKNG) technology company headquartered in Boston. As a regulated gaming company, you may be required to obtain a gaming license issued by the appropriate state agency as a condition of employment. Don't worry, we'll guide you through the process if this is relevant to your role. The US base salary range for this full-time position is 160,000.00 USD - 200,000.00 USD, plus bonus, equity, and benefits as applicable. Our ranges are determined by role, level, and location. The compensation information displayed on each job posting reflects the range for new hire pay rates for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific pay range and how that was determined during the hiring process. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

• Provide day-to-day support for Regulatory Affairs activities and operations. • Assist with document organization, information management, and administrative coordination. • Support internal documentation systems (e.g., SharePoint libraries). • Compile and maintain information for external reporting. • Assist with tracking regulatory/standards updates. • Contribute to exploratory improvement initiatives (including evaluation of new tools and workflows). • Gain hands-on experience with regulatory requirements relevant to innovative therapies (e.g., cell and gene therapies).

Role Description The Senior, Compliance & Monitoring supports the Compliance and Monitoring team by performing essential tasks related to the timely analysis, processing, and review of extensive grant compliance documentation required by federal and state regulations. The role provides first level compliance review and oversight, ensuring audit ready program records and adherence to applicable federal regulations. The Senior, Compliance & Monitoring reviews and validates data integrity, collaborates with program teams to resolve compliance issues, and communicates regulatory requirements to support consistent implementation. The incumbent delivers technical assistance, prepares compliance reports and presentations, and strengthens capacity building efforts by reinforcing internal controls and monitoring practices that support high quality compliance audits. The position requires strong analytical, communication, and problem-solving skills, as well as proficiency in technology and data analysis tools. Qualifications - Bachelor’s degree in Accounting, Business Administration, Finance, or Law from an accredited university, required - Advanced degree in Accounting or Finance, preferred - Three (3) or more years of professional office experience including finance, accounting, audit, and/or compliance, required - Experience in policy and compliance, emergency management, disaster recovery, mitigation, community planning, federally funded programs, housing, economic development, and/or infrastructure, preferred - Knowledge of federal funded programs, preferred - Knowledge of 2 CFR § 200 Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards, preferred - Knowledge of rural healthcare initiatives, preferred - Basic knowledge of Microsoft Office applications (Word, PowerPoint, Outlook, Excel), required - Proficiency in data analysis tools, preferred - Excellent verbal, interpersonal, and written communication skills - Effective data analysis, problem-solving, and decision-making capabilities - Ability to utilize program policies and procedures to quickly solve problems and ensure program compliance - Willingness to ask bold questions to inform policy, welcome feedback, and proactively collaborate with the team - Ability to meet daily and weekly production goals as set by the program - Strong collaboration skills and ability to work in a fast-paced environment - Self-starter dedicated to providing quality work in a timely manner - Ability to work in remote, office, or BDO offices as required - Ability to sit for prolonged periods and lift up to 15 pounds at times - Ability to travel to client meetings as requested Requirements - Assists program and project analysts in planning and conducting internal compliance reviews of all programs and functions, and prepares detailed reports - Performs first level review of grant compliance documentation to verify completeness, accuracy, and adherence to federal and state regulatory requirements, ensuring audit ready records - Contributes to the development and continuous improvement of compliance, monitoring, and internal control processes that support high quality grant oversight - Works closely with program teams to resolve identified issues to conclusion - Communicates applicable state and federal regulations to key stakeholders in collaboration with subject matter experts - Collaborates with internal teams, project staff, and consultants to identify and recommend training, technical assistance opportunities, insights, and expertise for policy, compliance, and other relevant training to staff and key stakeholders - Reviews internal and external presentations and reports on an ad hoc, bi-weekly, monthly, and quarterly basis - Accepts responsibility for accuracy of data entry, accumulation, and maintenance of program records - Supports subject matter expert team with other tasks and efforts as needed - Other duties as required Supervisory Responsibilities - Supports onboarding and training of new compliance or program staff by reinforcing regulatory expectations, documentation standards, and internal control practices - Assigns or coordinates compliance review activities and timelines to ensure timely completion of monitoring deliverables - Promotes a culture of accountability and continuous improvement by modeling high standards for compliance review, documentation, and issue resolution Benefits - Flexibility and opportunities for advancement - Employee Stock Ownership Plan (ESOP) that offers participants a stake in the firm’s success - Comprehensive compensation and Total Rewards benefits