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Job DescriptionCampus OSU-Center for Health Sciences Contact Name & Email Jamie Childers, Jamie.Childers@okstate.edu Work Schedule Typically, Monday - Friday 8 hour shifts Appointment Length Regular Continuous/Until Further Notice Hiring Range $ Salary Priority Application Date While applications will be accepted until a successful candidate has been hired, interested parties are encouraged to submit their materials by to ensure full consideration. About this Position This is a Grant Funded Position A Postdoctoral Fellow position is available in the laboratory of Dr. Swarup Mitra at Oklahoma State University Center for Health Sciences. This NIH-funded position is ideal for an ambitious and collaborative scientist interested in working at the intersection of neuroscience, gut microbiome biology, and neuroimmune signaling. Research Focus: Our laboratory investigates how interactions between the gut microbiome and the brain influence behavior, neural plasticity, stress susceptibility, and disease vulnerability. Current NIH-funded projects examine mechanisms by which microbial and host-derived signals influence neural circuits and cellular processes, including astrocyte and oligodendrocyte biology, neuroimmune signaling, epigenetic regulation, and behavioral adaptations. The successful candidate will have the opportunity to work across multiple experimental platforms and develop an independent research direction within the broader goals of the NIH-funded program Required Qualifications • A Ph.D. in Neuroscience, Molecular Biology, or Microbiology in Public Health, Clinical Psychology, Health Psychology, or a related discipline Ph.D./Ed.D. (degree must be conferred on or before agreed upon start date) Skills, Proficiencies, and/or Knowledge: • Good communication and interpersonal skills are preferred to facilitate interactions with faculty and students.

Job DescriptionDescription: The Laboratory Technician is responsible for performing analytical testing on raw materials, in-process samples, and finished agricultural chemical products to ensure compliance with company and customer specifications, regulatory requirements, and quality standards. This role supports manufacturing operations by providing accurate and timely analytical results, assisting operations in troubleshooting and providing a recommendation on products that are out-of-specification, and maintaining a safe and organized laboratory workspace. Essential Functions and Responsibilities • Perform routine physical and chemical analyses on raw materials, intermediates, and finished products according to approved test methods., • Conduct analytical testing using laboratory equipment such as pH meter, density meter, moisture analyzer, FTIR spectrometer, flashpoint apparatus, and inductively coupled plasma spectrometer (ICP)., • Perform routine calibration, verification, and preventative maintenance of laboratory equipment., • Ensure compliance with safety, environmental, and hazardous chemical handling procedures., • Maintain laboratory cleanliness, inventory of chemicals and consumables, and proper disposal of laboratory waste., • Support production by providing timely quality data to minimize manufacturing delays., • Promptly report all problems regarding procedures, specifications, etc., to Manager or Chemist., • Perform assigned duties independently while collaborating with cross functional teams to get the support needed., • Assist with special projects (i.e. testing for new products, enhancements to existing products, etc)., • Troubleshoot and recommend batch adjustments to Operations when products are found out-of-specification., • Identify and suggest process improvements to enhance efficiency., • Other duties as assigned.Requirements: Education • Bachelor's degree in chemistry, biology or a related field. Experience • 1-3 years of laboratory experience in quality control, chemical manufacturing, or related industry preferred. Knowledge, Skills, and Abilities • Knowledge of physical and analytical chemistry techniques and laboratory equipment, • Familiarity with ISO 9001, or similar quality management system, • Proficiency with Microsoft Office, • Experience working with laboratory equipment such as pH meter, density meter, moisture analyzer, FTIR spectrometer, flashpoint apparatus, and inductively coupled plasma spectrometer (ICP), • Understanding of how to safely handle and dispose of hazardous chemical, • Ability to work under time pressure, tight deadlines, and interruptions, • Strong analytical and troubleshooting skills, • Ability to make an informed recommendation based on data collected and/or provided, • Flexibility to work overtime as needed to support Operations Physical Requirements This is a safety sensitive position.

Job Description Oklahoma Arthritis Center (OAC) is an Equal Employment Opportunity employer and considers all applicants without regard to race, religion, color, sex, national origin, age, disability, veteran status, or any other legally protected status. Job Summary: Both Physician Assistant (PA) and Nurse Practitioner (NP) responsibilities involve providing a broad range of services that begin with an initial patient consultation and continue with ongoing care and assessment throughout the rheumatology clinical relationship. Essential Functions: Operating under direction of a Physician, the PA/NP will: • Order and interpret tests, counsel patients on preventive care, conduct physical examinations, and write prescriptions for rheumatology patients., • Contribute to practice effectiveness by identifying short-term and long-range patient care issues that must be addressed, providing information and commentary pertinent to deliberations, and recommending options and courses of action., • Assess patient health by interviewing patients, performing physical examinations, and obtaining, updating, and studying medical histories., • Determine abnormal conditions by administering or ordering diagnostic tests, such as x-rays, electrocardiograms, and laboratory studies and interpreting test results., • Document patient care services by charting in patient and department records., • Perform therapeutic procedures by administering joint injections or aspiration., • Instruct and counsel patients by describing therapeutic regimens., • Provide continuity of care by developing and implementing patient management plans., • Maintain safe and clean working environment by complying with procedures, rules, and regulations., • Protect patients and employees by adhering to infection-control policies and protocols., • Comply with federal/state/local legal and professional requirements by studying existing and new legislation, anticipating future legislation, enforcing adherence to requirements, and advising management on needed actions., • Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional societies., • Contribute to team effort by accomplishing related results as needed., • Build practice to support the vision and goals of OAC. Competencies: • Coachable., • Health Promotion and Maintenance., • Thoroughness., • Clinical Skills., • Communication Skills., • Medical Teamwork., • Physiological Knowledge., • Bedside Manner., • Infection Control., • Administering and ordering medication administration via IV infusion., • Pain Management., • Self-Development. Supervisory Responsibility: This position may supervise other medical staff as needed. Qualifications: • Bachelor’s degree preferably in a biology or other science or medical field., • Must be professionally licensed and be in good standing with all applicable federal/state/local licensing bodies., • 3 to 5 years of experience in clinical assessment of patients; preferably in rheumatology., • This position will be expected to maintain current knowledge of industry best practices, trends, and applicable federal and state laws regarding scope of practice. Physical Requirements: • Ability to work effectively in a fast paced environment., • Physical ability to sit, perform data entry, and view computer screen for long periods at a time., • Daily standing, walking, bending, and maneuvering., • May require lifting up to 50 pounds or more to transfer and/or turn patient with and without assistive devices. Environmental Conditions: Occasional exposure to communicable diseases and biohazards. This is a safety sensitive position. Travel Requirements: Travel to other OAC locations is expected for this position. Scheduled Working Hours: Normal work hours are 8:00 a.m. to 5:00 p.m., Monday through Thursday and 8:00 a.m. to 1:00 p.m. on Fridays. Hours may vary based on daily patient schedule. It may be required for the PA/NP to be available for supervising an infusion team on occasion. Weekend and holiday on-call hours are expected from time to time. Other Duties: Please note this job description is not designed to cover or to contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change from time to time, with or without notice. Equipment Operated: Computer, standard medical equipment, and various medical instruments.

Job DescriptionCampus OSU-Center for Health Sciences Contact Name & Email Jamie Childers, Jamie.Childers@okstate.edu Work Schedule Typically, Monday - Friday 8 hour shifts Appointment Length Regular Continuous/Until Further Notice Hiring Range $19.00 - $21.64 Hourly Priority Application Date While applications will be accepted until a successful candidate has been hired, interested parties are encouraged to submit their materials by to ensure full consideration. About this Position This is a Grant Funded role. The Hardesty Center for Clinical Research and Neuroscience seeks a full-time Research Assistant to support a portfolio of interventional clinical trials. The position combines participant recruitment with hands-on clinical research coordination, including conducting study visits, administering clinical assessments, and supporting study drug administration and safety monitoring for enrolled participants. Duties • Assist with participant recruitment and screening, including community and clinic outreach, telephone and in-person screening, and eligibility determination., • Conduct study visits with enrolled participants, including administering clinical assessments and questionnaires, collecting vital signs, monitoring and documenting study drug administration, and observing participants for adverse events and other safety concerns., • Build and maintain rapport with participants to support engagement and retention throughout the study period., • Accurately document study visit data in source documents and electronic data capture (EDC) systems., • Maintain compliance with study protocols, Good Clinical Practice (GCP), and Institutional Review Board (IRB) requirements., • Assist with regulatory documentation and maintenance of study files., • Assist with activities across multiple concurrent studies and protocols., • Work as a team member within the OSU Biomedical Imaging Center and an ‘extended team’ member in the labs of research faculty with which the Simmons Lab is affiliated.Required Qualifications, • Bachelor's, • Degree in psychology, public health, biology, nursing, or a related field, or an equivalent combination of education and experience (degree must be conferred on or before agreed upon start date) Skills, Proficiencies, and/or Knowledge: • Strong interpersonal and communication skills, with demonstrated ability to build trust and rapport with research participants., • Ability to work with diverse participant populations in a nonjudgmental, patient-centered manner., • Detail-oriented, with strong documentation and organizational skills., • Ability to manage multiple studies and protocols simultaneously and to prioritize competing deadlines., • Proficiency with standard office and data entry software.Preferred Qualifications, • Prior experience in clinical research, healthcare, or human subjects research., • Experience with electronic data capture systems, such as REDCap., • Experience collecting vital signs., • Phlebotomy experience or certification; training and certification are available to candidates without prior experience., • Prior experience working with participants with substance use disorders or other behavioral health conditions., • Experience with participant recruitment and retention in longitudinal or interventional studies. Skills, Proficiencies, and/or Knowledge: • Familiarity with Good Clinical Practice (GCP) and human subjects protection training.Working Conditions, • Risk of exposure to strong acids/bases., • Ability to lift and carry 20 pounds, stoop, reach, stand, walk, finger, grasp, feel, talk, hear, see, and perform repetitive motions with or without reasonable accommodations.

Job DescriptionDescription: This role will provide hands-on, in-depth experience in the collection and analyzation of agricultural data. Join our team to gain real-life experience in cutting-edge crop management, sustainable agricultural practices, and real-world problem solving! Primary Responsibilities · Organize field testing to include gathering of materials, marking rows, staking plots, mixing treatments, and tagging plants · Collect study-related observations and data · Organize data for statistical evaluation · Travel to regional field plot locations for data and picture collection · Assist with lab preparation of test samples · Special projects as needed · Other duties as assigned Requirements: · Currently enrolled in Bachelor’s degree in Agriculture, Biology, Environmental Sciences, Weed Sciences, or similar degree program required · Experience conducting fieldwork in agricultural or environmental research preferred · Familiarity with laboratory protocols, including sample processing and equipment handling · Willingness to obtain a Plant Pesticide Applicator certification · Excellent organizational skills · Willingness to obtain Drone Operator License · Willingness to travel (min. 50%) · Proficiency in standard office software · Valid driver’s license Physical Requirements · Ability to work outdoors in varying weather conditions, for several hours at a time · Ability to lift up to 50 pounds

Senior Director, Global BioPharma Business Development About Our Client Our client is a leader in precision medicine, advancing the use of molecular science, genomics, and AI to improve patient care and accelerate drug development. By partnering with biopharmaceutical companies, healthcare organizations, and research institutions, the organization delivers innovative solutions that support biomarker discovery, clinical development, translational research, and commercialization. This is an opportunity to join a high-growth business development team focused on building strategic partnerships with leading biotechnology and pharmaceutical organizations worldwide. Position Summary Our client is seeking a Senior Director, Global BioPharma Business Development to play a key leadership role in expanding strategic partnerships across the biotechnology, pharmaceutical, and healthcare sectors. The ideal candidate will bring deep expertise in genomics, precision medicine, diagnostics, real-world data, bioinformatics, and/or the drug development continuum—from early discovery through clinical development, medical affairs, and commercialization. Leveraging an established network of industry relationships, this individual will identify, develop, negotiate, and manage high-value strategic partnerships that drive long-term growth. This role will work closely with executive leadership and cross-functional stakeholders to develop commercial strategies, cultivate new business opportunities, and execute complex partnership agreements. Key Responsibilities • Develop and execute strategic business development initiatives across biopharma accounts., • Identify, qualify, and engage pharmaceutical and biotechnology partners through existing relationships and new business development activities., • Build a deep understanding of the company’s portfolio and align solutions with partner needs., • Structure and negotiate strategic collaborations, commercial agreements, and customized partnership models., • Generate qualified opportunities and manage them throughout the full business development lifecycle., • Prepare and deliver executive-level presentations, proposals, and business cases., • Lead commercial negotiations and support contract execution in partnership with legal and executive leadership., • Build and maintain long-term relationships with existing and prospective partners., • Collaborate closely with scientific, laboratory, bioinformatics, pathology, medical affairs, technology, and legal teams to develop partnership solutions., • Represent the organization at major industry conferences and partnering meetings, including events such as JPM, BIO, AACR, ASCO, SITC, and other relevant scientific conferences., • Achieve revenue growth through strategic partnerships and expansion of existing relationships. Required Qualifications • MBA or equivalent combination of scientific and commercial experience., • 10+ years of professional experience, including at least 7 years in biopharma business development, strategic partnerships, or commercial leadership., • Demonstrated success leading senior-level business development initiatives and closing complex, enterprise-scale partnerships., • Experience owning multimillion-dollar revenue targets and strategic partnership pipelines., • Strong commercial negotiation experience, including contracts, deal structures, and executive stakeholder management., • Proven ability to develop executive presentations, proposals, and commercial strategies., • Experience serving as the external face of an organization at industry partnering meetings and scientific conferences., • Excellent communication, presentation, and relationship management skills. BioPharma & Scientific Expertise The successful candidate will possess: • Strong understanding of pharmaceutical and biotechnology research and development processes., • Deep knowledge of oncology, precision medicine, molecular diagnostics, genomics, biomarker strategies, real-world data/evidence, clinical trials, and translational research., • Experience partnering with pharmaceutical and biotechnology organizations across research, development, medical affairs, and commercialization., • Working knowledge of molecular biology, drug discovery, diagnostics, or related scientific disciplines., • Ability to engage scientific, clinical, and executive stakeholders across the drug development continuum. Preferred Qualifications • PhD, MD, or equivalent scientific background preferred., • Entrepreneurial mindset with the ability to thrive in a fast-paced, high-growth environment., • Strong strategic thinking and problem-solving skills., • Exceptional written and verbal communication abilities., • Demonstrated success developing long-term strategic partnerships within the biopharmaceutical industry., • Highly collaborative, self-motivated, and results-oriented. Travel • Approximately 20–30% travel for partner meetings, conferences, and industry events. Compensation & Benefits • Base salary: $200,000–$230,000 + 25% bonus., • Comprehensive medical, dental, and vision benefits., • 401(k) with company match., • Generous paid time off and holidays., • Health Savings Account and Flexible Spending Account options., • Short- and long-term disability coverage., • Tuition assistance., • Employee Assistance Program., • Additional voluntary benefits, including pet insurance and legal assistance.

Job Type: Flexible Contract (Remote) Job Summary: We are hiring experienced biomedical scientists, including research scientists, clinical laboratory scientists, postdoctoral researchers, and advanced doctoral candidates, for a contract project that tests whether frontier AI agents can carry out real experimental biology work. You will design research-grade tasks drawn from your own laboratory practice that a leading AI model cannot solve, then review how and why the model fails. We are especially interested in scientists with hands-on flow cytometry experience. What you will do • Design self-contained tasks drawn from the practice of biomedical research, such as gating a multi-color flow cytometry dataset from raw FCS files, identifying the flaw in an experimental design, fitting and interpreting dose-response or enzyme kinetics data, performing quality control on a sequencing or mass spectrometry dataset, and reproducing a reported result and explaining a discrepancy., • Assemble the materials each task needs, including data files, protocols, and context, write a reference solution, and define clear criteria or automated checks that determine whether a solution is correct. Because biological data is noisy and analysis involves judgment, criteria need to be precise or use well-justified tolerances., • Run your task against a frontier AI agent, review its attempt with the same rigor you would apply to a manuscript under peer review, and refine the task until the failure reflects a real gap in the model's scientific capability rather than ambiguity or trick wording., • Work with reviewers to bring each task to acceptance. Who we are looking for • A PhD in biochemistry, cell biology, immunology, pharmacology, molecular biology, or a closely related field. Advanced doctoral candidates with substantial hands-on laboratory experience are also encouraged to apply., • Hands-on experience in at least one of the following areas: flow cytometry and immunophenotyping, cell-based and phenotypic assays, biochemistry and protein science, mass spectrometry, genomics and bioinformatics, structural biology and molecular modeling, or drug metabolism, pharmacokinetics, and preclinical safety., • Experience in research, clinical, or industry laboratory settings. Work in regulated environments, such as CAP or CLIA-accredited laboratories, counts fully toward this experience., • For flow cytometry candidates: experience analyzing raw data yourself, ideally including FCS files and FlowJo workspaces, rather than only overseeing analysis., • Working knowledge of Python or R for data analysis. Familiarity with the command line and Git is a plus., • Experience in assay development and validation, peer review, or designing course assignments and assessments is a strong advantage, because the work draws on the same skills. Why Cobalt AI: • Advance frontier AI where it counts. Apply your scientific expertise to the data that frontier labs cannot obtain any other way, where your reasoning directly shapes how the next generation of models works through experimental problems., • Grow professionally. Expand your influence through evaluation projects, advisory roles, and research collaborations, while deepening your understanding of how frontier models are trained and assessed., • Work with a top-tier network. Collaborate with scientists from leading institutions, biotech companies, and clinical laboratories on high-impact, flexible work., • Set your own schedule. Flexible 10 to 40 hour weeks that fit around your research position and your life., • Competitive pay. Rates vary by project and are determined by a number of factors, including scope, skillset, and experience.

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The editor will handle primarily Perspectives in biology. The editor works with the Visuals and Media teams to create striking explanatory graphics and multimedia, while ensuring excellent customer service to our authors. At least five years of experience as a commissioning editor with proven abilit

The successful candidate will combine expertise in computational biology, cancer genomics, and scientific analysis with product leadership, stakeholder engagement, and program management to drive the continued evolution of one of the world's leading myeloma-focused multi-omic research platforms. Com

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Advanced degree in biology, immunology, cell biology, biochemistry, or a closely related life sciences field. Review AI-generated answers to experimental biology problems end to end, including the experimental design, the methods, the data interpretation, and the final conclusion, and confirm that e

PhD in biology, immunology, cell biology, biochemistry, or a closely related life sciences field. Your judgment directly determines which tasks are used to measure what leading models can and cannot do in biology. Review AI-generated answers to experimental biology problems end to end, including the

Research Engineer, Biological Safety and Orthopedic Devices Location: Remote, US-based Preferred location: Denver, CO, with onsite work possible for local candidates We are looking for a Research Engineer to support investigation, research, and remediation activities for orthopedic medical devices. This role will focus on biological evaluation, preclinical research, risk assessment, technical documentation, and regulatory support. The successful candidate will work closely with R&D, Design Engineering, Process Engineering, Manufacturing, Quality, Regulatory Affairs, Corporate, and site teams. Key responsibilities • Support the remediation and lifecycle management of existing orthopedic products., • Develop, review, and approve study protocols, technical reports, and biological safety documentation., • Lead or support biological safety risk assessments in accordance with ISO 10993., • Develop strategies for technical investigations and provide scientific expertise to cross-functional teams., • Coordinate laboratory studies, preclinical testing, timelines, deliverables, and external collaborators., • Support biocompatibility assessments and biological safety testing., • Contribute biological safety content and technical rationale for regulatory submissions., • Present scientific and technical information to internal stakeholders, regulatory bodies, surgeons, key opinion leaders, and external experts., • Prepare project updates, technical reviews, data presentations, and research summaries., • Support cross-functional project planning, risk management, scope, timelines, and execution. Required qualifications • Master’s degree in Biomedical Science, Biology, Toxicology, Materials Science, or a related discipline., • PhD or DVM is preferred., • 5+ years of experience in medical-device R&D with responsibility for biological safety risk assessment, or equivalent experience., • 3 to 5 years of hands-on preclinical in vivo research, including large-animal model testing., • Strong knowledge of ISO 10993, biocompatibility, biological evaluation, and orthopedic-device requirements., • Experience supporting regulated product development and cross-functional research programs., • Demonstrated project-management experience., • Strong scientific writing, presentation, problem-solving, and stakeholder-management skills., • Ability to communicate complex scientific and regulatory topics clearly to technical and non-technical audiences. This opportunity is ideal for someone with strong expertise in biological safety, orthopedic devices, preclinical research, and regulated medical-device development.

Job DescriptionDescription: About US Neuro US Neuro is a nationwide provider of intraoperative neurophysiologic monitoring (IONM) and EEG services. We work closely with leading hospitals and surgical teams to enhance patient safety during complex procedures. Our commitment to clinical quality, responsiveness, and collaboration has made us a trusted partner in neuromonitoring since 2005. Position Summary We’re seeking a highly motivated individual to join our team as a Trainee Surgical Neurophysiologist. This is an entry-level opportunity that offers paid training and mentorship in the growing field of surgical neurophysiology. No prior neurodiagnostic experience is required—just a strong work ethic, a scientific mindset, and a passion for patient care. Responsibilities • Assist with patient prep, electrode application, and monitoring setup in the operating room, • Observe and support neurophysiological data collection during surgeries, • Participate in structured, supervised training to become CNIM-eligible, • Maintain accurate documentation and follow hospital safety and infection control protocols, • Travel between affiliated hospitals and surgical centers as needed What We Offer • Training and support for CNIM exam preparation, • Competitive salary and benefits, • Supportive team environment and long-term career growth, • Hands-on experience with diverse case types including spine and neuro procedures Requirements:, • Bachelor’s degree in neuroscience, biology, psychology, or related field (preferred), • Reliable, detail-oriented, and comfortable in a surgical/clinical setting, • Strong communication and teamwork skills, • Willingness to work early mornings and maintain a professional demeanor in high-stress environments, • Interest in pursuing CNIM certification