Job Closed

This listing is no longer active.

HelloBetter logo
HelloBetter

Leading provider of prescription digital therapeutics (PDTx) for mental health with the strongest evidence base globally

Clinical Lead Ello (f/d/m)

Clinical ResearchClinical ResearchFull TimeRemoteLeadTeam 51-200Since 2015H1B No SponsorCompany SiteLinkedIn

Location

Germany

Posted

81 days ago

Salary

€66K - €84K / year

Seniority

Lead

No structured requirement data.

Job Description

Clinical Lead Ello (f/d/m)

HelloBetter

General Information Team Lead: Dr. Alena Rentsch (Head of Content) Talent Acquisition: Celia Nielsen (People & Talent Partner) Contract: Permanent, 32-40 hours per week Start Date: 1 April 2026 or earlier Salary Range: 66k-84k € + VSOP (one-time, 15-20% of yearly salary) Remote Policy: Remote-first culture with offices in Berlin, Hamburg and Potsdam Your mission HelloBetter is a pioneer in the field of digital healthcare. For more than 10 years, we have been developing evidence-based digital health applications for the prevention and treatment of mental health conditions. Our applications cover a variety of areas, including stress management, depression, problematic alcohol use, panic disorder and anxiety, vaginismus, and sleep disorders. Six of HelloBetter's ten applications are approved as digital health applications. They are available free of charge by prescription to all insured adults in Germany. In 2025, we've launched Ello. Ello is HelloBetter's AI mental wellness companion that provides evidence-based psychological support for everyday mental health challenges like stress, low mood, and difficult life situations. We've combined our 10 years of digital therapeutics expertise with AI technology to make psychological support more accessible. For more information about HelloBetter, see our HelloBetter Handbook. As a Clinical Lead for Ello, your role is to bring clinical psychology expertise to AI. You'll be the clinical expert who ensures Ello provides safe, effective and evidence-based psychological support. This is a strategic clinical role that combines hands-on psychological work with cross-functional leadership - no coding or technical background required. Your objectives - Shape the Psychological Approach: You'll define how Ello should respond psychologically, determining when to explore versus offer support, how to maintain appropriate boundaries, and what makes conversations effective. Working with C-level leadership and teams across the company (including psychotherapists, research, product, engineering, and data science) you'll balance evidence-based practice with innovation and regulatory requirements. - Ensure Quality & Effectiveness: You'll ensure the psychological quality of Ello's conversational approach, collaborating with psychotherapists and researchers to identify what's working and what needs improvement. You'll design psychological protocols and quality standards, then guide the data science & engineering team on implementing your clinical insights while they handle the technical implementation. - Build the Evidence Base: You'll drive Ello's evaluation strategy together with our (User) Research Teams and head the systematic assessment of conversation quality from a clinical perspective. Collaborating with data scientists, you'll understand findings and drive improvements whilst helping establish scientific standards for this emerging field. - Own Psychological Safety: You'll support Ello's safety framework by working closely with our Senior Psychotherapist & Medical Risk Manager responsible for established risk management principles, to ensure appropriate crisis detection and escalation protocols. You'll monitor for potential risks and ensure appropriate safety mechanisms whilst maintaining clear boundaries between wellness support and situations requiring clinical care. - Communicate Clinical Value: You'll present Ello's approach and safety to potential clients such as employers and health insurers, explaining in accessible terms why our evidence-based approach differs from generic AI chatbots. You'll support commercial teams in articulating clinical value to diverse stakeholders. Your profile Must Haves - Licensed psychotherapist (approbation or equivalent) with foundation in evidence-based approaches - Understanding of psychological assessment, intervention design, and therapeutic mechanisms - Track record developing, evaluating, or delivering digital mental health interventions - Understanding of how therapeutic principles translate to digital environments - Ability to comfortably work and form a strategic vision at the frontier of psychology and AI where best practices don't yet exist - Ability to translate clinical requirements into technical specifications and business value - Experience navigating different working styles and finding common ground across multiple disciplines, e.g., clinical, technical, and business Nice to Haves - PhD in the field of psychology with a focus on digital mental health (or comparable topic) - Experience balancing ideal clinical standards with practical business and technical constraints - Understanding of technical concepts (prompt engineering, model behaviour, system architecture) - Experience working across technical, clinical, and commercial functions Why us? Meaningfulness - Mental health is a human right: we help thousands of people each month who struggle with depression, stress, insomnia, burnout, and other mental health issues Research & Evidence - We have a unique product and are at the forefront of research in digital health applications - The effectiveness of our product is continuously evaluated and efficacy studies have been published in international and high-impact journals since 2014 - Data is of great importance to us and we are transparent about our strategy, goals and results. Growth - As pioneers in the development of applications for various mental health conditions, we are at the forefront of innovation - We operate in an extremely exciting and emerging market - Annual training budget of 1,000 euros - we place great emphasis on the personal growth of our employees and actively support their development Remote-First - Remote-first culture - we hire globally, considering a time window of +/- 4.5 hours CET - Use of our offices in Berlin and Hamburg if you prefer to work on-site - Relocation option and support Diversity & Inclusion - Fair and equal treatment are the standards of our Anti-Harassment Policy - Flexible working hours - shape your own day - Company language English, with a strong emphasis on inclusive language - Transparent salary bands - Additional 10 paid leave days for non-birth parents after the birth or adoption of a child Other Benefits - 28 vacation days + compensation for holidays that fall on weekends - Tenure based paid time off - up to three additional days - Permanent employment contract - Attractive VSOP (Virtual Stock Option Plan) for all employees - Tax-deductible pension plan with an above-average employer contribution - Free or subsidized fitness memberships - Regular team events HelloBetter is an equal opportunity employer and encourages applicants of any national origin, gender, sexual orientation, religious background, gender identity, and people with disabilities to applyPrivacy Policy for Applicants Interview Process - Call with the People Team (30 mins) - Technical Interview with Alena & Elena (60 mins) - Take-Home Case Study (2-3 hours) - Team Interview with Tanja & Vincent (30 mins) - Founder Interview with C-Level (15-30 mins)

Related Categories

Related Job Pages

More Clinical Research Jobs

ICON plc logo

Clinical Trial Manager

ICON plc

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.

Full TimeRemoteTeam 10,001+Since 1990H1B No Sponsor

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures. • Build and manage strong relationships with trial investigators and stakeholders. • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines. • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Spain
Job Closed
ICON plc logo

Centralized Clinical Trial Manager

ICON plc

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.

Full TimeRemoteTeam 10,001+Since 1990H1B No Sponsor

Centralized Clinical Trial Manager ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Centralized Clinical Trial Manager to join our diverse and dynamic team. As a Centralized Clinical Trial Manager at ICON, you will play a crucial role in effectively reviewing site visit reports as per Protocol and ICON and Sponsor SOPs and to ensure the quality of reports are of the highest standards , errors are minimized and that issues are escalated as appropriate. You will be responsible for follow up on action items and protocol deviations and to be a liaison between CRA, CTM and PM for timely resolution of issues. You will act as an extension of the CTM/CTM team for the specific purpose of visit report review and approval''. Location: Bangalore or Chennai ( Home Based or Office Based) What You Will Be Doing: - To effectively review visit reports as per Protocol and ICON and Sponsor SOPs and to ensure the quality of reports are of the highest standards , errors are minimized and that issues are escalated as appropriate - To follow up on action items and protocol deviations and to be a liaison between CRA, CTM and PM for timely resolution of issues. - To act as an extension of the CTM/CTM team for the specific purpose of visit report review and approval. - To observe and escalate safety trends in patients as identified in visit report - Recognize, exemplify and adhere to ICON's values which center around our commitment to People, Clients and Performance . - As a Manager, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. - Effectively review and approve visit reports as per annotated report, protocol, ICON and/or Sponsor SOPs and ensure errors are minimized , reports are consistent across visits and sites and adhere to the highest standards of quality . Ensure turnaround time of the visit reports per contract, ICON and or Sponsor SOPs - Regular oversight of OMR , ICO trial (and where required Sponsor CTMS and vendor systems) to ensure key metrics, e.g. MVR and FUL timelines, Action Items and other quality metrics are being met and followed-up as necessary Ensure open action items and protocol deviations are escalated and followed up for timely resolution as per contract or corporate standards . - Where required , attend project meetings and actively provide suggestions for improvement of quality of reports, provide feedback for timely and appropriate resolution of action items and report trends • - Liaise with CTM to communicate any trends , outstanding issues, safety concerns or any other activity or lack thereof which may jeopardise the clinical trial delivery or patient safety . - Ensure all necessary trainings , required to improve job performance managing people and project or process related issues which are necessary to perform successfully in a service oriented environment. - Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. • Fluent in written and spoken English. - Computer literate. - Ability and willingness to travel if required - Extensive use of telephone expected continuous improvement in trial processes. Your Profile: - Bachelor’s degree in life sciences, healthcare, or a related field (advanced degree preferred). - Minimum 8-10 years of Clinical Research experience with at-least 5 years of on-site monitoring experience. - Experience in On-Site Monitoring and Clinical Trial Management, with a solid understanding of on-site monitoring approaches. - Strong analytical skills with proficiency in clinical trial data review and interpretation. - Excellent organizational and project management skills, with the ability to manage multiple studies and meet deadlines. - Effective communication and interpersonal skills, with the ability to collaborate across diverse teams and functions. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

India
Job Closed
Komplex Care logo

Clinical Nurse Manager

Komplex Care

Komplex Care stands at the forefront of national care provision, delivering high-quality, nurse-led, person-centred care in the comfort of our clients' homes. We specialise in supporting both adults and children with complex conditions ranging from but not limited to spinal injuries, brain injuries & behaviour that may challenge. We strive to provide tailored complex care with a personal touch. Our mission is simple: to empower individuals to lead fulfilling, independent, and dignified lives. Every client receives dedicated attention from their own Operations Manager and Registered Nurse, ensuring continuity, compassion, and the highest standards of care in their preferred environment. We are equally committed to our team, offering meaningful training, continuous support, and genuine opportunities for career development.

Role Description Are you an experienced nurse passionate about the delivery of exceptional care in the community? Do you thrive on leading multidisciplinary teams and developing others? If so, we want to hear from you. Komplex Care is looking for a dedicated and skilled Clinical Nurse Manager to join our team. In this vital role, you’ll lead and manage complex care packages in clients’ homes, providing high-quality, person-centred care that promotes independence and respects individual dignity. What You’ll Be Doing - Delivering personal, practical, social and emotional care to clients with complex needs in their own homes - Designing, delivering and reviewing tailored care plans for each individual - Providing ongoing clinical assessments and support for clients' physical and psychological needs - Leading and supervising care staff, ensuring high standards of clinical practice and compliance - Coordinating and communicating effectively with the MDT, families, and external stakeholders - Delivering specialist clinical training to staff and carers within care packages - Attending and contributing to clinical governance and management meetings at Head Office - Promoting and upholding the values of dignity, respect, and independence in every interaction Qualifications - Registered Nurse (NMC) with up-to-date PIN - Experience in complex care, particularly with tracheostomy and ventilator care (training provided) - Strong leadership, mentoring, and clinical teaching skills - Excellent communication and interpersonal abilities - Understanding of safeguarding, risk assessment, and care planning - IT literacy (Microsoft Office & care database systems) - A full UK driving licence and willingness to travel Desirable Skills & Qualifications - Mentoring qualification - Experience in community nursing or working with MDTs - Familiarity with clinical governance frameworks and audit processes Benefits - Pension Scheme for long-term security - 24/7 GP access for you, your partner, and children (up to 18) - Free mental health support for you, your partner, and children (up to 18) - Life insurance for peace of mind when it matters most - Home life advice line for everyday guidance - Career development opportunities - Wellbeing videos and guided meditations - Earn points for staying active - Vouchers for Amazon, Tesco, Nike and more - Up to 33% off gym memberships - Employee of the Month recognition with a £50 voucher Join Us At Komplex Care, we’re proud to make a real difference in people’s lives every day. If you’re ready to take the next step in your nursing career and lead with compassion, professionalism, and clinical excellence, apply now to join a team that puts people first.

United Kingdom
Job Closed
Full TimeRemoteTeam 10,001+Since 1949H1B Sponsor

We anticipate the application window for this opening will close on - 3 Apr 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life We are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. At Medtronic, the Clinical Specialist, supports the Neuromodulation Pain and Target Drug Delivery as well as Interventional Therapies (in some districts) in the areas of surgical coverage, follow-up support, troubleshooting, customer service and education.  This person will be engaged in basic market development activities depending upon the needs of the assigned territory and district.   This is a field based role. Responsibilities may include the following and other duties may be assigned: - Represents Medtronic as device specialist during surgical procedures by ensuring all necessary equipment and products required are available, providing technical support and device selection, and performing programming and testing of all device systems - Manages patients through all phases of the clinical process as well as educate them on the features and benefits of Medtronic products - Provides clinical support in surgeries, re-programmings, trouble-shooting and follow ups in hospitals and clinics - Educates and trains physicians, hospital personnel and office staff on products and therapies. This is expected by, but not limited to, coordinating one on one teaching sessions, formal in-services, education programs, seminars and/or outside symposia (based off quarterly Plan of Action as directed by Leadership) - Responds promptly and professionally to device-related inquiries by customers and patients - Ability to be flexible with schedule while working and/or attending clinical events, possibly outside of normal business hours to include weekends and after hours and at the discretion of Clinical Specialist Manager - Adheres to company policies and complies with required event reporting and documentation, utilizing Medtronic technology tools - Responsible for managing inventory provided for case coverage, including:  timely transactions when product is used, sold or transferred, maintaining a required level of cycle count accuracy, executing product retrievals as instructed, turning over inventory in a reasonable time frame, not implanting expired product or product that is on hold - Contributes to the achievement of quarterly goals associated with specific initiatives at the district, regional and/or national level by partnering with colleagues and communicating effectively and regularly    with Leadership - Maintains a working knowledge of competitive products - Regularly visits accounts to establish/maintain relationships with office staff and Health care providers - Accountable for placing orders with customer service for pending purchase orders and product replacement - Expected to work with materials management to collect POs for cases covered within the territory/district - Ensures personal understanding of all quality policies/system items that are personally applicable - Assists Management and Sales Training department in education/training of new employees within the district - Effectively utilizes Excel, a mobile phone, an IPAD, a laptop, and/or a Samsung tablet regularly - Manages business expenses and budget effectively and in given timeframe  - Mentors Associate Clinical Specialists - Completes all new hire therapy trainings as directed by medical education - Completes all corporate compliance training prior to date due - Travels to cover district cases as needed in the district, and occasionally to other districts at the discretion of Clinical Manager   The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.    We seek out and hire a diverse workforce at every level: We need fresh ideas and inclusive insights to continue to be an innovative industry leader —that’s why we make it a point to seek out, attract and develop employees who are patient-centric, passionate, and who represent the same wide variety of life experiences as our patients.   To learn more about Inclusion & Diversity at Medtronic Click Here Qualifications Must Have: Minimum Requirements To be considered for this role, please ensure these minimum requirements are evident in your applicant profile. -  A High School Diploma or GED with a minimum of 6 years of clinical or medical sales experience; or -  An Associate’s Degree with a minimum of 4 years of clinical or medical sales experience; or -  A Bachelor’s degree with a minimum of 2 years of clinical or medical sales experience. Nice to Have: Preferences -  Bachelor's degree in a health care related field -  Master’s degree -  Registered nurse or HCP with experience in a sterile environment -  Clinical experience with implantable neurological products and patient care -  Experience in servicing medical personnel on product use -  Experience with a medical device company or pharmaceutical company, and clinical experience in a specialty area: neurology, neurosurgery,  orthopedic, operating room, pain management, or home health care - Understands basic reimbursement and healthcare environment - Excellent organizational skills and ability to work under pressure - Preference will be given to local qualified candidates and candidates with Medtronic experience   Additional Job Requirements: •  Required to function using healthcare universal precautions to minimize exposure to infectious disease and radiation •  Ability to serve as the primary resource for scheduled and unscheduled clinical events, periodically required to work weekends, evenings and nights and may be required to engage in overnight travel within own district or neighboring districts •  Ability to work efficiently and autonomously with little direction when outside of clinical events •  Ability to attend national meetings, district meetings and other training as requested •  Ability to wear a 7-9 lbs  protective lead apron for extended periods of time in the operating room •  Ability to lift up to 40 lbs •  Ability to sitting, standing, and/or walking for 8+ hours per day •  Ability to bend/stoop, squat and balance frequently •  Specific vision abilities required by this job include close vision, distance vision, depth perception, and ability to adjust focus in relation to travel and operating a personal computer.   **Must have a valid driver's license and active vehicle insurance policy. In addition, your driving record will be reviewed and will be considered as part of your application.       Business Description: Our vision is to become the undisputed world leader in Neuromodulation, improving patient lives through innovative solutions. Our therapies span the care continuum; from early interventional procedures to implantable surgical technologies that relieve pain, restore function and improve lives for our patients. We're committed to applying clinical and economic evidence and integrated technologies to our unmatched portfolio of therapies to develop healthcare solutions that increase patient access, improve the efficiency of procedures and deliver successful patient outcomes.​ The Neuromodulation Operating Unit offers solutions — from early interventional procedures to implantable surgical technologies — that treat chronic pain as well as pain from spinal fractures, cancer, and severe spasticity.​ Our key Pain Therapies include: Spinal Cord Stimulation, Drug infusion for Chronic Pain / Drug infusion for severe Spasticity,  and RF Nerve Ablation. Our key Interventional Therapies include: Balloon Kyphoplasty, Vertebroplasty, RF Ablation (for bone) and Microwave Ablation (for soft tissue).   Click here to learn more about our entire Neurological product portfolio. #LI-MDT For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.  The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Salary ranges for U.S (excl. PR) locations (USD):$68,000.00 - $102,000.00 The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). In addition to Base Salary, this position is eligible for a Sales Incentive Plan (SIP), which provides the opportunity to earn significant incentive compensation for achieving or exceeding your goals. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums). Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico. Further details are available at the link below: Medtronic benefits and compensation plans About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here. It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities. If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

United States
$68K - $102K / year
Job Closed