Role Description CLOVEHITCH is currently seeking Certified Medical Interpreters to support a potential federal healthcare language services requirement. Interpreters will provide over-the-phone interpretation and/or video remote interpretation for patient-provider communication in a military medical environment. - Provide accurate, complete, and impartial medical interpretation. - Support communication between healthcare providers, staff, patients, and family members. - Interpret medical terminology, patient instructions, treatment discussions, and healthcare-related information. - Support over-the-phone interpretation and/or video remote interpretation. - Provide word-for-word interpretation without summarizing, omitting, or adding content. - Maintain confidentiality of patient information. - Follow HIPAA, privacy, and professional interpreter ethics requirements. - Be available for scheduled, urgent, and on-call assignments, including nights, weekends, holidays, or surge support as needed. Qualifications - Current Certified Medical Interpreter (CMI) credential required. - Demonstrated medical interpreting experience. - Familiarity with specialized medical terminology and healthcare procedures. - Ability to support remote interpretation assignments. - Professional conduct and strong communication skills. - Ability to complete or provide HIPAA / Privacy Act training documentation. - Ability to pass exclusion screening, including HHS OIG LEIE and TRICARE Sanctioned Provider List checks. - Prior federal healthcare, military treatment facility, hospital, clinic, emergency department, or urgent care experience preferred. - Experience supporting over-the-phone interpretation preferred. - Experience supporting video remote interpretation preferred. - Availability for 24/7, night, weekend, holiday, and surge coverage preferred. - This position is open only to individuals authorized to work in the U.S. without sponsorship. Physical Demands - This position may require extended periods of speaking and active listening. Position Type & Hours of Work - Work is requested on an on-call, as-needed basis. - Availability for nights, weekends, and holidays may be required. Travel - Work is performed remotely via over-the-phone or video remote interpreting platforms. - No on-site travel is required. Company Description CLOVEHITCH is a Service-Disabled Veteran-Owned Small Business focused upon providing professional solutions in the areas of training and talent acquisition.

Role Description Assures the credentialing of healthcare providers is conducted in accordance with organizational policies, operational procedures, and applicable governmental and regulatory agency regulations and standards. Performs activities associated with verification, tracking inquiries, and follow-up on problems which may delay completion of the file. - Obtains source verification of credentials in accordance with prevailing policies and procedures. - Tracks responses and follows-up on items not received within established cycle periods. - Reviews completed files with management in accordance with established schedules. - Maintains credential records. - Produces management reports regarding operations performance and/or provider credentialing status for internal management and external providers using the health system's verification services. - Adheres to operating policies and procedures including delivery of completed work and use of resources. - Initiates correspondence to providers, users, health plans and others as necessary to obtain requisite credentialing information. - Informs management regarding the status of departmental operations and provider credentialing issues of concern. - Performs related duties as required. All responsibilities noted here are considered essential functions of the job under the Americans with Disabilities Act. Duties not mentioned here, but considered related are not essential functions. Qualifications - Associates degree required, or equivalent combination of education and related experience. - 1-3 years of relevant experience, required. - Position is remote. Company Description The salary range and/or hourly rate listed is a good faith determination of potential base compensation that may be offered to a successful applicant for this position at the time of this job advertisement and may be modified in the future. When determining a team member's base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).

• Maintain responsibility for the execution and oversight of the region’s clinical operations functions • Drive regional adherence to our evolving clinical tenets • Own full P&L for region(s) • Manage fixed costs • Assist in improving upon the strategy and framework for aligning the clinical assessment • Drive accountability to clinical outcome measure completion • Ensure high-quality and ethical care • Oversee adherence and compliance with external regulations • Drive regional clinical and compliance improvement at the center level • Lead, develop, mentor and engage a team of center leads • Serve as the regional clinical subject matter expert • Foster a metrics driven culture

Title: Medical Safety Lead (client-dedicated), EMEA Location: Remote EMEA Full time The Medical Safety Lead is going to lead and perform the assessment of medical safety data for assigned products, develop and execute safety signaling and benefit-risk management strategies, closely collaborate with stakeholders internally (e.g. Regulatory Affairs, clinical development, medical affairs) and externally (e.g. Key Opinion Leaders or regulatory agencies) to align safety communications and to ensure the safe use of client`s products. A day in the Life: - Provide strategic medical safety leadership and practical contributions for assigned product(s) in a cross-functional setting - Perform safety signal management and benefit risk assessment activities as well as other regular and/or ad-hoc aggregate safety data reviews as needed for assigned product(s) - Lead cross-functional teams to perform regular and/or ad-hoc review of existing and emerging aggregate safety data for assigned product(s) - Contribute to the development of the overall safety governance structure and activities - Provide safety strategies and deliver accurate, timely and high-quality safety contributions for the preparation of relevant sections of regulatory submission documents globally (e.g. ISS, SCS, narratives) for assigned product(s) - Prepare and/or review safety sections of clinical/regulatory documents (including study protocols, IBs, Clinical Study Reports, or ICFs) - Provide medical safety support for the preparation of responses to regulatory authority inquiries. Assure that safety information is timely, complete, and accurate - Lead the overall preparation of periodic safety reports (e.g. PSUR, DSUR); provide medical safety content and ensure consistency and quality of these documents - Oversee the medical assessment of individual case safety reports (ICSR) - Confirm criteria and content for expedited reporting and unbinding (e.g. SUSAR or urgent safety issues) - Lead or actively contribute to the preparations and presentation of safety information to the Data Safety Monitoring Board (DSMB) - Provide medical safety contributions at internal audits and regulatory inspections - Support the development of and updates to GPS Standard Operating Procedures (SOPs) and other controlled documents (e.g. work instructions, forms, templates) - Support adverse event reporting training and pharmacovigilance awareness activities cross functionally - Support the preparation of pharmacovigilance agreements with clinical development or commercial business partners - Participate in cross-functional teams and initiatives Keys to Success: - Strong scientific and analytic skills - Ability to complete multiple tasks concurrently and deliver results in a fast-paced environment - Strong ability to lead, motivate, influence, and collaborate with multidisciplinary teams - Excellent presentation skills with the ability to communicate complex issues clearly Education and Experience: MD required. History of an active medical license highly preferred. Candidates should have: - Clinical experience in having direct responsibility for diagnostic and treatment decisions (2+ years); - Direct experience in medical review and assessment of safety information/Pharmacovigilance (5+ years). Knowledge, Skills and Abilities: - Working knowledge of relevant pharmacovigilance regulatory requirements and guidance documents - Demonstrated ability to perform medical assessments of safety data from multiple sources - Experience with authoring complex documents and contributing to regulatory submissions - Knowledge of adverse event reporting systems - Experience in epidemiology, biostatistics, clinical development, or medical affairs is a plus