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Hiring remote Field Clinical Engineers/Specialists in the Souththeast region of the USA. About Recor Medical At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise™ uRDN System, we are on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe. Position Summary: The primary purpose of the Clinical Field Specialist role is to build a clinical patient pipeline for Recor-sponsored clinical studies. This role partners with clinical sites to expand the referral base and drive patient recruitment through targeted, data-driven outreach and education. The Field Clinical Specialist also provides procedure support including case proctoring, physician certifications, and site qualification visits. Responsibilities and Duties Drive Provider Referral Program: • Analyze claims and EMR data to identify high-potential providers and patient populations., • Develop and execute targeted outreach and education programs with site teams. Guide EMR Patient Identification & Reporting: • Collaborate with investigators and research coordinators to define and validate EMR flagging criteria; provide hands-on support to sites for implementing and optimizing flags within their systems., • Collaborate with site teams to generate targeted patient lists for chart review by leveraging EMR data and predefined eligibility criteria. Procedure & Training Leadership: • Proctor cases and certify physicians on protocol and device use; deliver hands-on training and maintain compliance records. Site Qualification & Activation: • Plan and conduct Site Qualification Visits (SQV) and Site Initiation Visits (SIV) with CRA/PM to ensure activation requirements are met and Day-1 recruitment workflows are ready. Cross-Functional Problem Solving: • Collaborate with Clinical Ops, Medical Affairs, Quality/Regulatory, and Commercial teams to remove enrollment barriers and improve site performance. Requirements: • Bachelor’s degree in Life Sciences, Nursing, or related field., • 4+ years' experience in clinical research, site management, or field clinical support., • Strong knowledge of GCP, FDA regulations, and cardiovascular procedures., • Proven ability to lead training programs and manage complex site workflows., • Excellent communication, data interpretation, and relationship-building skills. Preferred Qualifications: • Clinical Research Coordinator (CRC) certification or equivalent clinical research training, • Experience as a Field Clinical Engineer or similar technical role., • IDE trial experience and hypertension knowledge., • Proficiency with EMR systems and clinical trial platforms. Salary range: $121K - $150K (Annual Base Salary) (Commensurate with experience, skills, education, and training) Pre-Employment Requirement At Recor Medical, patient safety and compliance are at the heart of everything we do. To support these standards, employment for all field-based roles is contingent upon successfully completing a pre-employment background check and drug screen. These steps help ensure we bring the highest level of integrity and accountability to the physicians and patients we serve. Radiation Safety Requirement Certain field-based roles at Recor Medical require work in environments where radiation sources (e.g., x-ray equipment) are in use. Employees in these roles will be issued a personal dosimetry badge to monitor occupational exposure and are required to wear it in accordance with company policy and applicable regulatory standards. This program is designed to ensure compliance with federal and state regulations and to maintain radiation exposure at levels that are As Low As Reasonably Achievable (ALARA). Additional guidance and protective equipment, as necessary, will be provided as part of onboarding and ongoing safety training. About Recor Medical At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise™ uRDN System, we are on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe. Position Summary: The primary purpose of the Clinical Field Specialist role is to build a clinical patient pipeline for Recor-sponsored clinical studies. This role partners with clinical sites to expand the referral base and drive patient recruitment through targeted, data-driven outreach and education. The Field Clinical Specialist also provides procedure support including case proctoring, physician certifications, and site qualification visits. Responsibilities and Duties: Drive Provider Referral Program: • Analyze claims and EMR data to identify high-potential providers and patient populations., • Collaborate with investigators and research coordinators to define and validate EMR flagging criteria; provide hands-on support to sites for implementing and optimizing flags within their systems., • Collaborate with site teams to generate targeted patient lists for chart review by leveraging EMR data and predefined eligibility criteria. Procedure & Training Leadership: • Proctor cases and certify physicians on protocol and device use; deliver hands-on training and maintain compliance records. Site Qualification & Activation: • Plan and conduct Site Qualification Visits (SQV) and Site Initiation Visits (SIV) with CRA/PM to ensure activation requirements are met and Day-1 recruitment workflows are ready. Cross-Functional Problem Solving: • Collaborate with Clinical Ops, Medical Affairs, Quality/Regulatory, and Commercial teams to remove enrollment barriers and improve site performance. Requirements: • Bachelor’s degree in Life Sciences, Nursing, or related field., • 4+ years' experience in clinical research, site management, or field clinical support., • Strong knowledge of GCP, FDA regulations, and cardiovascular procedures., • Proven ability to lead training programs and manage complex site workflows., • Excellent communication, data interpretation, and relationship-building skills. Preferred Qualifications: • Clinical Research Coordinator (CRC) certification or equivalent clinical research training, • Experience as a Field Clinical Engineer or similar technical role., • IDE trial experience and hypertension knowledge., • Proficiency with EMR systems and clinical trial platforms. Salary range: $121K - $150K depending on location and experience. The successful candidate's starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.

The PRN Sub-Investigator (Sub-I) plays a critical role in clinical research by supporting the Principal Investigator (PI) in the oversight and conduct of clinical trials. Depending on qualifications and site delegation, this role may also be eligible to be hired as either a Sub-I or a PI. The primary duty of the Sub-I/PI is to protect human subjects and uphold their rights throughout the clinical trial. This role ensures that all delegated study activities are conducted in accordance with the protocol, Good Clinical Practice (GCP), and applicable federal regulations, while maintaining the integrity and validity of all data collected. This role is part time and estimated be 10-15 hours a week on site in Hollywood, FL. Duties and Responsibilities: • Attends Site Initiation Visits and/or training in-service for all current protocols., • Completes required SOP training., • Performs physical exams on research subjects., • Performs study tasks delegated by the Principal Investigator (PI) with full involvement and oversight in accordance with protocol and regulatory requirements., • Provides guidance to the clinical team as needed., • Assists in the training of support staff for the clinical trials under supervision., • Assists in recruitment for clinical trials; refer to other site trials., • Sets schedule to accommodate patients onsite and/or offsite as necessary. This may include weekends and holidays., • Conducts proper informed consent process according to SOPs, ensuring the most current ICF version is used., • Evaluates the eligibility of patients for inclusion into clinical trials., • Collects medical and surgical history, concomitant medication use, and adverse event information., • Documents source documents, inpatient activities, visit progress notes, and adverse events. Maintains accurate records throughout the study., • Reviews lab results, provides clinical significance for any out-of-range or abnormal values, and signs off as appropriate., • Evaluates appropriateness of patient inclusion into trials; order repeat labs if necessary, or screen-fail patients as needed. Counsels’ patients on seeking appropriate medical care when necessary., • Reinforces study restrictions, diets, and study guidelines., • Reviews and provides insight into impending CRFs, electronic CRFs, data clarification forms, and/or data queries., • Reviews source documents, lab results, and procedures throughout the study., • Assesses adverse events and drug reactions, thoroughly recording details, including the relationship to the study drug., • Assists in reporting any serious adverse events (SAEs) to the PI., • Participates in monthly staff meetings., • Reads and understands the information in the Investigator's Brochure (IB), including the potential risks and side effects of the drug., • Performs Clinical Research Coordinator duties., • Occasional travel to Company sites, Investigator meetings, and/or Company meetings., • Performs other miscellaneous job-related duties as assigned by your manager. This job description is not an exhaustive list of all the functions that you may be required to perform. The Company reserves the right to revise this job description at any time. Requirements: • A qualified Nephrologist in the relevant field of health care (MD), • Must be credentialed with Davita and Fresenius Kidney Centers., • Minimum of 3 years’ experience in clinical research (preferred), • In-depth knowledge of federal regulations regarding responsibilities of a Primary or Sub- Investigator. The Investigator is deemed competent when he/she can thoroughly manage project, read and understand the available information (IB) on the product under investigation, including the potential risks and side effects of the drug and possesses the ability to adhere to the study protocol and investigate the drug under investigation. Competency Requirements: • Excellent communication skills., • Problem-solving skills., • Planning/organizational skills., • Customer service skills., • Attention to detail and ability to follow clinical research protocols., • Ability to work collaboratively with a multidisciplinary research team., • Strong analytical and critical thinking skills., • Adaptability to a fast-paced research environment., • In depth knowledge of FDA-GCP regulations pertaining to protecting human rights and safety, ethical issues and clinical assessments when dealing with clinical research and human volunteers.

Job Summary Under direction of the Senior Manager of Clinical Trial Operations, the Clinical Research Coordinator II, CTO (CRC II) manages and conducts the day-to-day activities of a research study. In general, the CRC II ensures the study maintains accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements. Beyond administrative duties, responsibilities of a CRC II may include subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, collection and reviewing study data to enter it into the study and site systems, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities. Job Specific Duties • Attends and participates in investigator meetings, pre-study visits, and initiation meetings or coordinator meetings as appropriate., • Collects and maintains accurate patient data for submission to Sponsor, maintaining proper patient records, coordinating the collection, and shipments of specimens as required by protocol., • Communicates study objectives/procedures to relevant hospital units involved with the study including the establishment of good rapport with the Principal Investigator & providing required assistance., • Communicates with the Sponsor or their representatives, schedules and facilitates study monitor visits, and facilitates communication between Principal Investigator and Sponsor or Sponsor’s Representatives., • Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff., • Interacts with patients and families to recruit (screen, consent and enroll) study subjects and ensures compliance with the protocol., • Responsible for speedy and adequate patient enrollment as determined by Research Management and Principal Investigator in all assigned studies., • Submits new protocols to Research Regulatory Affairs team (for IRB submission/approval) and verifies proper document were received with the proper format., • Demonstrates and utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol., • Follows NCRIs Standard Operating Procedures, AAHRPP, HIPAA, and FDA guidelines for clinical research, and keeps updated in those procedures and/or guidelines., • Enters required data into CTMS., • Provides new Protocols, Amendments, and study status updates to necessary research staff for digitization/entry into CTMS., • Works adjusted hours to accommodate subject visits. The ideal candidate has experience with Hematology/Oncology. Minimum Job Requirements • Bachelor's degree and 2 years of research experience (OR) Associate's degree and 4 years of research experience, • Experience in pediatric clinical research in a hospital setting., • Clinical research certification (CCRC, CCRP, CRA) and IATA certification preferred., • Experience working on clinical trials, interventional studies is preferred, • Bilingual in English/Spanish., • Excellent communication skills in working with both children and adults., • Excellent organizational skills, detail-oriented, people-oriented, flexible, and adaptable to change., • Time management skills., • Knowledge of protocols and its process., • Experience with software applications including word processing, scheduling and contact database, email, web browsing, hospital records, other database software and office equipment., • Experience with relevant hospital equipment for each clinical trial project., • Availability to work adjusted hours to accommodate subject visits.

Job Description Patient Care America is a premier renal healthcare provider specializing in precision medicine nutrition support and clinical solutions for kidney disease patients. We offer evidence-based therapies such as IDPN (Intradialytic Parenteral Nutrition) and IPN (Intraperitoneal Nutrition) to help manage malnutrition and improve clinical outcomes. Backed by published research demonstrating improvements in albumin levels, our therapies are trusted by nephrology teams and dialysis clinics nationwide. Proudly accredited by PCAB, ACHC, and NABP, we uphold the highest standards of safety, quality, and care. But our commitment extends far beyond delivering infusion therapies; our value-added services include oral nutrition supplement programs, access to our clinical support nurse team, patient support networks and free continuing education for registered dietitians and nurses. As a leading renal solutions provider, we also offer bundled prescription medications, streamlining delivery and supporting improved medication adherence. To support patients beyond the clinic, we provide digital tools and community-based platforms tailored to their needs and experiences. These tools include educational resources, the TransplantLyfe365 app, and an online peer community () that helps patients connect with others and manage the everyday challenges of chronic kidney disease and transplantation. Driven by a dedicated commitment to scientific rigor, clinical excellence and compassionate care, Patient Care America is redefining what it means to be a true partner through each stage of kidney care. BENEFITS Our company offers: • Competitive pay, • Monthly bonus program, • Generous paid time off, • Paid holidays, • Health insurance, • Life insurance, • Employer paid Long-term and Short-term Disability, • Wellness, • 401k retirement with company matching program, • Educational assistance, • Career growth JOB SUMMARY: The Technician Group Lead has day-to-day responsibility for the coordination and supervision of Pharmacy Technicians and Pharmacy Support staff (if assigned) including providing operational expertise, assistance when needed and guidance in the compounding and administrative areas of the pharmacy. Duties including data entry into the pharmacy software system, sterile compounding and prescription processing, filling, and labeling under the direction of the Pharmacist Team, participation in hiring and training of new staff, training existing staff, implementing pharmacy processes, and adhering to the policies and procedures of the company, the State’s pharmacy regulations, and other regulatory entities. QUALIFICATIONS: • Current, valid Pharmacy Technician license issued by the State of Florida., • Minimum of 10 years of pharmacy technician experience preferred., • PTCB Certification required., • Advanced Certified Pharmacy Technician (CPhT-Adv), Certified Compounded Sterile Preparation Technician (CSPT) required or an equivalent of 5+ years advanced-level experience in workflow optimization, training, or sterile compounding, • Minimum 2 years’ experience in management/supervisory role required., • Pharmacy Technician Immunization Certification preferred., • Experience working in a fast-paced, deadline driven environment preferred., • Self-motivated, able to work independently, with minimal supervision., • Detail oriented; strong organizational skills., • Ability to multitask and prioritize effectively., • Effective problem-solving skills., • Ability to handle complex situations., • Ability to create and analyze reports., • Excellent interpersonal skills to maintain relationships with both internal and external customers., • Excellent verbal and written communication skills., • Strong customer service skills., • Ability to work as part of a diverse team and promote a positive team environment., • Experience with Microsoft Office (PowerPoint, Excel, etc.) required., • Strong computer skills and ability to master any company utilized software programs., • Advanced knowledge of and compliance with all pharmacy and company policies and guidelines., • Experience teaching and training others., • Knowledge, understanding, and implementation of USP Chapter 797 including cleanroom maintenance and documentation requirements., • Successful completion of Texas Sterile Compounding and Aseptic Technique program., • Proficiency in pharmaceutical calculations., • High level pharmacy software system skills (super user capabilities), • Strong knowledge of administrative operations., • Maintain professionalism at all times., • Accurately enter data, new prescriptions and compounding instructions, process refills, process formula changes, create delivery tickets and compounding worksheets, process new patient starts, perform appropriate calculations (IPN, IDPN, all Rx), complete assigned tasks (“To-Do’s”) into pharmacy-specific software., • Maintain patient profiles, enter progress notes, attach documents and enter lab values into pharmacy-specific software., • Answer phone calls and handle/triage appropriately., • Perform quality checks of daily patient orders, boxes, bins and delivery tickets., • Work with warehouse to complete a final review of shipments., • Communicate effectively through email and by telephone with other departments and customers/patients., • Utilize appropriate resources to effectively solve problems., • Accurately and efficiently compound sterile preparations using approved aseptic technique for pharmacist review., • The ability to properly clean and maintain the sterile compounding room, anteroom, workroom including all equipment and train other staff members per USP 797 guidelines, Florida State Board of Pharmacy regulations, and company policies and procedures when needed., • Successfully complete media fill testing and gloved fingertip testing annually/as needed and assist the Lead Cleanroom Pharmacist and/or IV Cleanroom Specialist in overseeing the process for all compounding staff to ensure timely completion., • Develop, conduct and complete annual didactic training and process validations including any ongoing training or re-training of all team members., • Oversee and participate when needed in all daily cleanroom activities including sanitizing and stocking to ensure consistent level of minimum compounding productivity standards., • Completely and accurately document clean room activities and assume responsibility to ensure all documentation requirements are met daily/weekly/monthly per company policies and procedures., • Coordinate, conduct and oversee training of new technicians and existing staff regarding sterile compounding, cleaning and administrative duties., • Develop a training schedule and materials for newly hired employees and conduct/participate in the training., • Coordinate and participate in monthly inventory., • Coordinate and participate in routine check of expiration dates., • Participate in the on-call rotation as scheduled., • Comply with all state and federal regulations and all company policies and procedures., • Comply with all HIPAA and privacy policies and practices., • Assist management in creating team building activities and maintaining a positive work environment. Participate in all activities., • Utilize analytical abilities to prepare and present reports/metrics for all departments including Finance, Pharmacy/Warehouse/DME, IT, etc., • Collaborate with management to identify trends, suggest workflow improvement suggestions, implement process improvements and implement department changes for improved efficiency and safety., • Maintain proficiency in all company policies and procedures and assist management with review and development as needed., • Develop and present in-services for areas that require improvement or training., • Coordinate and prepare the staff schedule including holiday planning and the on-call schedule for final approval by the Pharmacy Operations Manager., • Coordinate and assign/schedule technician and support staff daily administrative duties including task list, patient/clinic calls, refills, etc. Ensure refills, new starts, formula changes, discharges etc. are processed on time/ahead of time., • Schedule, train and oversee assigned staff members., • Maintain and update the Pharmacy Technician and Pharmacy Support Training Manuals., • Assist the Pharmacy Operations Manager with competencies, orientation checklists, 90-day reviews and annual evaluations., • Assist the Pharmacy Operations Manager in the interviewing/hiring of Pharmacy Staff., • Participate in all department and company meetings; conduct and hold technician and support staff meetings on a regular basis., • Assist Pharmacy Licensing Coordinator with any tasks that may require their expertise., • Work with the Pharmacy Operations Manager, Lead Administrative Pharmacist, and Lead Cleanroom Pharmacist on projects and initiatives as requested. This includes all lines of new pharmacy technology (NewLeaf, Smartsheets, etc.) and be able to work directly with management and the staff on new initiatives and lines of business (Parata, transplant medications, etc.).

Job DescriptionMedical Research Coordinator (Full Time) - Hollywood, FL (Spanish-speaker) We are looking for an experienced, bilingual (Spanish-speaking) Medical Research Coordinator to join our research team in Hollywood, FL. The Medical Research Coordinator will be responsible for the coordination of clinical research studies while ensuring compliance with all applicable regulations and guidelines. The ideal candidate will possess a strong understanding of clinical research, clinical trials, and the medical field. The Medical Research Coordinator should have excellent communication, organizational, and problem-solving skills with an ability to prioritize tasks effectively. Responsibilities • Develop and maintain clinical study documents and coordinate all aspects of clinical trials including case report forms, informed consents, and other regulatory documents., • Monitor clinical trials and ensure that they are conducted in accordance with protocols, standard operating procedures, and applicable regulations., • Train, support and delegate tasks to clinical research staff., • Conduct data review and analysis., • Develop and manage budgets, timelines, and communications., • Ensure compliance with all applicable federal, state, and local regulations., • Maintain accurate records of research activities and submit reports to the appropriate authorities., • Develop and implement strategies for data collection., • Work with study investigators to ensure that the study is conducted in compliance with the protocol., • Develop study-related materials and provide support to investigators., • Provide guidance to investigators on the interpretation and implementation of the protocol., • Coordinate and participate in monitoring visits., • Perform other duties as assigned.Requirements, • Healthcare related background, such as FMD (Foreign Medical Doctor) NP, LPN, or RN., • At least two years of experience as a Clinical Research Coordinator., • Proficient in Spanish., • Excellent communication, organizational, and problem-solving skills., • Ability to prioritize tasks effectively., • Ability to work independently and as part of a team., • Ability to work in a fast-paced environment., • Knowledge of applicable federal and state regulations., • Knowledge of clinical research processes and procedures. The HealthPlus Team

Job Description GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and committed to ensuring protocol compliance and participant safety. Key Responsibilities: * Oversee all aspects of clinical trials from start-up to close-out * Coordinate patient visits, informed consent, and data collection * Ensure regulatory compliance and accurate documentation * Liaise with sponsors, CROs, and internal teams Qualifications: * 2+ years of experience as a CRC in a clinical research setting * Strong understanding of GCP, FDA regulations, and IRB processes * Excellent organizational and communication skills

Job DescriptionSalary: $15.00 - $20.00 per hour Medical Assistant- Patient intake; recording medical history and Informed Consent • Assist physician in exam rooms, • Answer phones and schedule appointments., • Keep exam rooms stocked with adequate medical supplies, maintain instruments, prepare sterilization as required, • MUST BE FLUENT IN ENGLISH AND SPANISH Job Type: Full-time Potential advancement as a Clinical Research Coordinator. Work Remotely • No Job Type: Full-time Salary: $12.00 - $19.00 per hour Schedule: • Monday to Friday Work Location: One location

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Brid

The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. The University of Miami/UHealth Department of SCCC CRS has an exciting opportunity for

Certification and Licensing: Current Research Coordinator certification by the Association of Clinical Research Professionals or Society of Clinical Research Associates for a minimum of 6 months. The Clinical Research Coordinator 3 serves as an experienced clinical research professional responsible

Job Description Job Title: Clinical Rater Job Description We are seeking a Clinical Rater to work with individuals with acute diagnoses such as schizophrenia, bipolar disorder, PTSD, OCD, anxiety, and depression. This role involves performing clinical and neurocognitive evaluations and interviews, administering and scoring tests that assess cognitive, neuropsychological, behavioral, and emotional status. Responsibilities • Administer clinical rating scales to study participants to confirm diagnoses and assess levels of psychopathology and function., • Complete organizational queries related to clinical scales and neuropsych ratings., • Utilize interpersonal and clinical skills for the management of study participants across various neuroscience therapeutic areas., • Participate actively in acquiring ongoing knowledge and instruction., • Assist management in maintaining a positive and motivated work environment., • Support the Principal Investigator (PI) in maintaining data integrity from clinical rating scales and neurocognitive testing., • Ensure continuity of data collection during staff absences, including documentation of consensus between backup and primary ratings., • Conduct clinical research consensus rounds for accurate signal detection with clinical subject ratings., • Participate in assessing prescreened and screening patients per PI's discretion and protocol., • Complete study-specific training in a timely manner., • Ensure adherence to best practices, FDA regulations, ICH, GCP, company guidelines, and policies., • Proficiency in clinical assessment with acute psychiatric conditions., • Bilingual in Spanish and English, with effective communication skills in both languages., • Minimum 2 years of clinical experience with the mental health population., • Experience working in clinical research, particularly as a Rater or Clinical Research Coordinator (CRC) in acute psychiatric studies., • Foreign language skills are advantageous, ideally a psychiatrist. The role operates Monday to Friday from 8:00 am to 4:30 pm, with on-call duties on weekends on a rotating schedule approximately once a month. The position requires flexibility in handling 3-7 studies at a time, with a patient volume of 1-7 per day. The work involves patient assessments, report writing, and follow-ups. A professional and adaptable attitude is essential. Job Type & Location This is a Permanent position based out of Hollywood, FL. Pay and Benefits The pay range for this position is $80000.00 - $95000.00/yr. Benefits package available. Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas. Workplace Type This is a fully onsite position in Hollywood,FL. Application Deadline This position is anticipated to close on Mar 18, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.