Role Description As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. - Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. - Involved in all stages of the clinical study, including: - Identifying potential sites to participate in the research effort. - Performing various study start-up activities such as working with sites to collect appropriate regulatory documents. - Supporting the negotiation of contracts and budgets. - Training the sites to collect data properly and report any potential safety-related events. - Managing the site's activities during study maintenance. - Closing down research activities at the sites once the study has concluded. - Conduct study initiation visits (SIVs). - Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements. Qualifications - Excellent interpersonal, oral, and written communication skills in English. - Superior organizational skills with attention to detail. - Ability to work with little or no supervision. - Proficiency in Microsoft Office, CTMS, and EDC Systems. Requirements - 5+ years of experience as a Clinical Research Associate. - 4-year university degree OR Nursing Degree. - Experience in CNS/Neurology is required; Psychiatry is strongly preferred. - Candidates must reside on the West Coast. - Willingness to travel regionally required. Benefits - Competitive salary range: $97,000.00 - $193,000.00 annually. - Competitive benefits package depending on location. - Pay equity and transparency.

Role Description As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including: - Cardiovascular - Metabolic - Neuroscience - Oncology - Rare Diseases Your contributions will leave a profound impact on the lives of patients. Responsibilities include: - Managing the research activities at sites participating in Worldwide’s clinical research projects - Involved in all stages of the clinical study, including: - Identifying potential sites to participate in the research effort - Performing various study start-up activities such as working with sites to collect appropriate regulatory documents - Supporting the negotiation of contracts and budgets - Training the sites to collect data properly and report any potential safety-related events - Managing the site's activities during study maintenance - Closing down research activities at the sites once the study has concluded - Conducting study initiation visits (SIVs) - Ensuring compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements Qualifications - Excellent interpersonal, oral, and written communication skills in English - Superior organizational skills with attention to detail - Ability to work with little or no supervision - Proficiency in Microsoft Office, CTMS, and EDC Systems Requirements - 2 - 5 years of experience as a regional, traveling Clinical Research Associate - 4-year university degree OR Nursing Degree - Experience in Oncology is required - Willingness to travel regionally required Benefits - Competitive salary range: $79,500.00 - $158,500.00 annually - Transparent compensation structure - Competitive benefits package depending on location - Pay equity and transparency

Role Description As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including: - Cardiovascular - Metabolic - Neuroscience - Oncology - Rare Diseases Your contributions will leave a profound impact on the lives of patients. Responsibilities include: - Managing the research activities at sites participating in Worldwide’s clinical research projects. - Involvement in all stages of the clinical study, including: - Identifying potential sites to participate in the research effort. - Performing various study start-up activities such as working with sites to collect appropriate regulatory documents. - Supporting the negotiation of contracts and budgets. - Training the sites to collect data properly and report any potential safety-related events. - Managing the site's activities during study maintenance. - Closing down research activities at the sites once the study has concluded. - Conducting study initiation visits (SIVs). - Ensuring compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements. Qualifications - Excellent interpersonal, oral, and written communication skills in English. - Superior organizational skills with attention to detail. - Ability to work with little or no supervision. - Proficiency in Microsoft Office, CTMS, and EDC Systems. Requirements - 2 - 5 years of experience as a regional, traveling Clinical Research Associate. - 4-year university degree OR Nursing Degree. - Experience in Psychiatric monitoring is required. - Willingness to travel regionally required. Benefits - Competitive salary range: $79,500.00 - $158,500.00 annually. - Transparent compensation structure. - Competitive benefits package depending on location. - Pay equity and transparency. Company Description We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Role Description Activated Insights is growing, and we're looking for friendly, reliable individuals throughout the Greater Idaho Falls area to join our team. This position offers flexibility, consistency, and a chance to make a difference. - Conduct phone surveys with clients, family members, and caregivers - Accurately document feedback - Create positive experiences for survey participants - Help organizations improve care and employee satisfaction Qualifications - Friendly and professional communication skills - Comfortable spending time on the phone - Reliable attendance - Basic computer proficiency - Ability to work independently from home Requirements - English fluency is required - Spanish-English and Russian-English bilingual candidates are strongly encouraged to apply and are highly valued Benefits - Work from home - Flexible scheduling - No nights, weekends, or major holidays - Consistent part-time hours (16–30 hours per week) - Paid training - Monthly bonuses and incentives - Paid Time Off - Supportive leadership and team culture - Competitive Pay: $11/hour + bonuses for team members working 25+ hours per week; $10/hour + bonuses for team members working 16–24 hours per week