Role Description Mercor connects elite creative and technical talent with leading AI research labs. The position is for Physics PhD Experts specializing in Advanced Quantum, Electrodynamics & Classical Mechanics. - Develop high-quality data for AI models by creating challenging problems in Advanced Quantum Mechanics, Advanced Electrodynamics, and Advanced Classical Mechanics. - Evaluate and improve AI model outputs through rigorous physics expertise and complex instruction adherence. - Collaborate with AI research teams to enhance training data quality and drive innovation. - Work independently and asynchronously to meet deadlines and contribute to cutting-edge projects. Qualifications - PhD in Physics with specialization in Advanced Quantum Mechanics, Advanced Electrodynamics, or Advanced Classical Mechanics. - Graduate degree from US/UK/Canada/Western Europe. - High attention to detail. - Exceptional written and verbal communication skills. - Excellent proficiency in English. Requirements - Contract position. - Compensation: $70–$90/hour. - Location: Remote. - Commitment: 4–6 tasks/week. Benefits - Flexible work schedule. - Opportunity to work on cutting-edge projects. Application Process - Upload resume. - AI interview based on your resume. - Submit form. For details about the interview process and platform information, please check: Interview Process Details . For any help or support, reach out to: support@mercor.com . PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Role Description Novant is looking to add a Research Analyst who has solid experience in Research and Beacon. Clinical experience would be highly preferred. The main role will involve building treatment plans. This will be a 3-month Contract to Hire role, and the manager wants the candidate to start ASAP. Qualifications - Epic systems - Epic research - Epic beacon - Clinical experience Requirements - Expert level experience Benefits - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)

Role Description We are seeking a highly organized and detail-oriented Research Assistant to support clinical and behavioral research studies. The ideal candidate will assist with regulatory documentation, digital file management, participant coordination, and remote data support. This position works closely with the Principal Investigator (PI) and research team to ensure compliance with study protocols and regulatory requirements. Key Responsibilities - Remote Study Coordination & Participant Support - Coordinate research activities in accordance with IRB-approved protocols. - Assist in identifying and screening potential participants based on eligibility criteria. - Support remote workflows related to participant tracking, consent documentation, and scheduling. - Help ensure adherence to FDA regulations, Good Clinical Practice (GCP), and institutional policies. - Regulatory & Digital File Management - Maintain and update IRB protocols and prepare regulatory documents for submission. - Assist in drafting and revising informed consent forms and other study materials. - Track and organize essential regulatory documents in secure digital formats to ensure compliance with FDA CFR and GCP guidelines. - Support collection and reporting of adverse events (AEs) and serious adverse events (SAEs) in coordination with the PI. - Prepare for and support internal reviews or audits by maintaining accurate digital records. - Data Support & Documentation - Assist with compiling and organizing behavioral and neuropsychological data for analysis. - Maintain secure, well-organized digital records and study documentation. - Generate summary reports and assist with research scheduling and documentation tasks. Qualifications - Bachelor’s degree in neuroscience, psychology, public health, or a related field; Master’s preferred. - Prior experience with human subjects research and knowledge of IRB, FDA, and GCP requirements. - Strong organizational and written communication skills. - High level of comfort working with digital tools (e.g., Google Workspace, Microsoft Office, secure cloud storage). - Ability to work independently and collaboratively in a fully remote setting. Work Schedule Opportunity for flexible scheduling. Availability for virtual meetings during standard business hours is required. Anticipated Pay Range Duke University provides an annual base salary range for this position as USD $51,448.00 to USD $77,945.00. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer. Benefits Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/ Equal Opportunity Employer Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, (including pregnancy and pregnancy related conditions), sexual orientation, or military status. Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas—an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values. Essential Physical Job Functions Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267).

Role Description When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Typical Accountabilities: - Contributes to the selection of potential investigators. - In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include: - Site Qualification Visits - Collection, preparation, review and tracking of documents for the application process - Submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study. - Trains, supports, and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principles. - Confirms that site staff have completed and documented the required trainings appropriately, including ICH-GCP training, prior to and for the duration of the study. Ensures the sites are inspection ready at all times. - Actively participates in Local Study Team (LST) meetings. - Contributes to National Investigators meetings, as applicable. - Initiates, monitors and closes study sites in compliance with client’s Procedural Documents. Shares information on patient recruitment and study site progress (site quality/performance) within the LST. - Drives performance at the sites. Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate. - Updates CTMS and other systems with data from study sites as per required timelines. - Manages study supplies (ISF, etc), drug supplies and drug accountability at study site. Prepares study drug for destruction, if applicable. - Performs monitoring visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Monitoring Plan. If required, determines and discusses with LSAD the correct timing and type of visits. - Performs Source Data Review (SDR), Case Report Form (CRF) review and Source Data Verification (SDV), in accordance with the Monitoring Plan. - Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study. - Ensures data query resolution in a timely manner. - Works with data management to ensure robust quality of the collected study data. - Ensures accurate and timely reporting of Serious Adverse Events and their follow ups. - Prepares and finalises monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator, including follow-up letter, within required timelines and in line with client’s SOP. - Follows up on outstanding actions with study sites to ensure resolution in a timely manner. - Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, CSP or ICH-GCP compliance issues to Local Management and/or CQM as required. - Assists site in maintaining inspection ready ISF. - Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and CQAD. - Ensures timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, client SOPs and local requirements. - Supports/participates in regular QC checks performed by LSAD or delegate. - Ensures that all study documents under their responsibility (i.e., site documents, relevant communications, etc) are available and ready for final archiving and completion of local part of the eTMF. - Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. - Ensures compliance with client’s Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). - Ensures compliance with local, national and regional legislation, as applicable. - Collaborates with local MSLs as directed by LSAD or line manager. Qualifications - Bachelor degree in related discipline, preferably in life science, or equivalent qualification. - Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. - Good knowledge of relevant local regulations. - Good medical knowledge and ability to learn relevant client’s Therapeutic Areas. - Basic understanding of the drug development process. - Good understanding of Clinical Study Management including monitoring, study drug handling and data management. - Excellent attention to details. - Good written and verbal communication skills. - Good collaboration and interpersonal skills. - Good negotiation skills. - Ability to travel nationally/internationally as required. - Valid driving license (to be deleted if not required in a country). Requirements - Ability to work in an environment of remote collaborators. - Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business. - Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time. - Good analytical and problem-solving skills. - Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines. - Familiar with risk-based monitoring approach including remote monitoring. - Good cultural awareness. - Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment. - Team oriented and flexible; ability to respond quickly to shifting demands and opportunities. Key stakeholders and relationships Internal (to client or team) - LSADs and Local Study Teams - Line Manager and local SMM LT - Clinical Quality Associate Director - Local Medical Teams: MSLs and Medical Affairs - Global Study Teams - Global Clinical Solutions functions - Clinical Data Management - Regulatory Affairs - Patient Safety External (to client) - Investigators and site personnel - Study related vendors - Inspectors