Role Description We are currently seeking a dedicated and experienced RPSGT with NY Licensure to score NY sleep and HSAT studies on a PRN basis. Reporting to the Manager of the Clinical Support Department, the Clinical Support Specialist will provide essential clinical and technical assistance to the MedBridge Healthcare team and contribute to our Home Sleep Testing (HST) department, ensuring the highest standard of care for our patients with sleep disorders. - MUST HAVE NY LICENSURE - MUST have a current RPSGT - MUST reside in one of the following states: CT, DC, DE, FL, GA, MD, NC, NJ, NY, PA, and VA. Primary Responsibilities will include: - Evaluating study data quality for in lab and HST studies - Score HST, MSLT, MWT, PSG, SPLIT, and PAP studies - Analyze data that has been acquired during the polysomnographic (sleep) study - Comply with applicable laws, regulations, guidelines, and standards regarding safety and infection control issues - Other clinical duties as required - Maintain strict confidentiality Qualifications - High School diploma - Registered Polysomnographic Technologist (RPSGT) credential holder - Licensure in the states that require Licensure for scoring of diagnostic tests (as-needed) - BLS/CPR-certified - Minimum of two years’ experience in scoring of sleep studies - Minimum two years’ experience with HST devices - Knowledge of all aspects of polysomnography and sleep medicine protocols - If working remotely, access to high-speed internet - Skill in use of computer and software - Skill in appropriate quality control and confidentiality procedures - Skill in analyzing data and situations to implement and administer procedures and to resolve technical, administrative, and patient related problems - Ability to learn and use multiple sleep software programs - Ability to exercise independent judgement for decision making and discretion - Ability to analyze complex situations and apply policy - Ability to communicate effectively and work collaboratively with staff - Ability to educate staff, patients, and families effectively Requirements - MUST HAVE NY LICENSURE - MUST have a current RPSGT - MUST reside in one of the following states: CT, DC, DE, FL, GA, MD, NC, NJ, NY, PA, and VA. Benefits - MedBridge is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability. - The affirmative Action Plans for Minorities and Women, Individuals with Disabilities and Protected Veterans are available for inspection, by appointment, with Human Resources during regular business hours upon request. - If you are an individual with a disability who may require an accommodation may contact Chad Henderson or at email address mhenderson@medbridgegroup.com, or dial TTY: 711 (Relay). - This employer participates in E-Verify. Federal law requires all employers to verify the identity and employment eligibility of all persons hired to work in the United States.

Role Description This role will be working within our Functional Service Partnership (FSP) team, fully embedded into our client partner where you will be working remotely in Europe. The position may require approx 20% travel to Belgium and the USA. The Pharmacoepidemiologist will be primarily responsible for generating real-world data (RWD) with a focus on safety. They will identify evidence gaps, develop methodology, and oversee the conduct of real-world studies. This role involves collaboration across functional areas, fostering continuous improvement, and engaging with external stakeholders, including vendors and key opinion leaders (KOLs). This role combines medical/scientific expertise, data analytics, and strategic thinking to ensure product safety while maintaining compliance with regulatory standards. The main purpose is to design and execute Pharmaco-Epidemiology activities and studies addressing safety research questions in the context of drug development, regulatory submissions, and marketed products. This will include data mining and analyses using various external sources such as claims data, electronic health records, registries, PAS, or others. You will collaborate with internal and external stakeholders and other decision makers to lead the planning, design, and any other contribution(s) to real-world studies. You will collaborate with internal teams who monitor the safety of products and relevant competitor safety profile(s), and who provide insights into differentiating aspects, and evidence gaps. Role Responsibilities: - Design and execute Epidemiology studies addressing safety research questions. - Identify epidemiological/pharmaco-epidemiological methods, relevant data sources, best suited to address safety research questions. - Conduct feasibility, design, prepare study concepts, protocols, and statistical analysis plans, and report of pharmacoepidemiologic studies. - Transfer epidemiologic expertise and deliverables to the evaluation, refinement and contextualization of safety findings. - Utilize analytical methods to interpret real world data, support the identification of safety data gaps in order to generate relevant insights. - In collaboration with key functional areas (RWE, Medical Affairs, GPS, Regulatory, HEOR, Clinical Development, Clinical Science), contribute to the development of Integrated Evidence Generation Plans (IEGPs). - Communicate safety RWD internally and externally promptly with all relevant stakeholders. - Collaborate with Scientific Communications on integrated publication plans for safety evidence. - Foster a continuous learning/improvement with all internal/external stakeholders. - Attend relevant internal and external meetings for training, competitor intelligence, and collaboration with KOLs and other experts. Qualifications - Background in health and life sciences (epidemiology, public health, MD, pharm D), or quantitative data sciences, biostatistics. - PhD in Epidemiology and/or pharmacoepidemiology or equivalent advantageous. - At least 5-year experience in epidemiology/pharmacoepidemiology as well as in drug safety. - Excellent written and oral communication skills in English. - Strong medical/scientific background, inspired by prioritizing patient safety. - Good working knowledge of both GCP and GVP. - Substantial prior experience of working with RWE/D within the pharmaceutical industry, particularly in the application of RWE in drug development for rare indications is a plus. - Ability to travel up to 20% of time as needed. Requirements - Proven experience including a track record in executing pharmacoepidemiology studies using RWD. - Highly developed analytical skills to understand complex matrix linkages of safety data from various sources. - Collaborative with strong communication, interpersonal, and leadership skills. - Proven track record of working and communication successfully within a complex multi-disciplinary environment. - Strong active listening skills with ability to incorporate input from a variety of internal and external stakeholders. - Drives initiative with ability to work with minimal supervision. - Good organizational skills and “hands on” attitude, reliable and solution oriented. - Effective in setting clear priorities among competing activities. - Embraces innovation by constantly seeking new ways to get results in different situations. - Proactively evaluates and participates in ongoing professional development opportunities. Benefits - When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. - You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. - Apply today to help us deliver tomorrow’s breakthroughs.

Title: Senior Compositors - must be located in Europe/UK Location: Stuttgart BW DE Job Description: We have great new opportunities for experienced mid and senior level Compositors to join our team here at Pixomondo working on a remote basis on a short contract starting ASAP Responsibilities: - Create high quality digital composites and visual effects for assigned shots, seamlessly integrating the various layers of a shot - Establish looks and/or follow set style direction - Understand and follow production guidelines, solving design and/or effect challenges for key visual effects shots as needed - Review and implement feedback quickly and effectively - Collaborate with Supervisors and other compositors to ensure shots are delivered to highest standard and on schedule Requirements - 3+ years of compositing experience on feature film and high-end television - Expert knowledge of Nuke - Knowledge of 3D and stereo compositing, CG integration with multi-pass EXR - Reel showing strong artistic skills including a sense of color, lighting, composition - Strong artistic skills including a strong sense of color, lighting, perspective, scale, and composition - Excellent attention to detail and desire to deliver consistently high-quality work, and encourage those around you to the same standards - Experience with Shotgun an asset - Excellent problem-solving skills - Excellent communication and interpersonal skills - Ability to work within a strong team environment Additional Requirements: - Visa sponsorship is not possible for this position - Please include your current resume, reel breakdown and a link to your demo reel and rate Benefits Pixomondo is an equal opportunity employer. We evaluate qualified applicants without regard to race, colour, religion, sex, national origin, disability, veteran status, age, sexual orientation, gender identity, or other protected characteristics.

Role Description This position will be working within OES, for Aston Online (in association with Aston University, Birmingham). Aston Online delivers world-class learning through degrees specifically designed for the online student. Each degree is tailored to provide opportunities for students who are often unable to undertake university studies on campus. At Aston Online, the student is at the forefront of everything we do. This role is an opportunity to support and guide our students through their learning journey. Our Online Tutors are the subject matter experts who facilitate the student’s learning, with a focus on helping them achieve their goals. The Opportunity We are looking for Online Tutors to work with our Aston Online BSc and MSc Psychology student cohorts. We are looking for people able to teach in the following areas: - Developmental - Cognitive - Biological - Neuropsychology - Social - Individual Differences - Clinical/health psychology - Qualitative and Quantitative Research Methods What You Will Do - Providing an exceptional student experience through the delivery of academic content developed by our partner academics and our learning design team. - Facilitating activities that engage and support student learning. - Undertaking assessment tasks (including moderation, marking, and feedback) as well as processing and submitting results according to set timelines. - Undertake three 30‑minute personal tutoring sessions across the tutees’ level of study (tutees may be enrolled on modules other than the one being taught). Benefits - 100% remote work - Flexible hours to fit around your other commitments (availability to login daily Monday to Friday is required) - The ability to use your discipline expertise to help others achieve their goals. - The opportunity to develop your online teaching skills within a forward-thinking innovative organisation. - A supportive and connected team to grow and develop within. Qualifications - You will hold a BPS accredited degree in Psychology (or equivalent) and a demonstrable track record in research or other scholarly activity in a field relevant to the modules you will be delivering. - A PhD either in progress or near completion as a minimum. - You will have experience in teaching and assessing at degree level. - You have high standards and with demonstrable impact on students’ learning. - You are motivated by student success and passionate about online learning. - You are a passionate and excellent, clear communicator. - You have strong presentation skills and the ability to maintain an engaging and positive online presence. - You are proactive and organised. - You thrive in a remote working environment. Requirements - Experience of using Virtual Learning Environments as learning tools. - Experience of teaching and assessing online programmes. - Be at least a fellow of Advance HE. - Experience using Qualtrics or Pavlovia. Now is your chance to join a highly engaged workforce and make a positive impact on the experience of our students! If you're interested, please apply now with a CV and cover letter explaining how you match up with the role requirements above and why you want to work as an Online Tutor with OES.