Jobs at Centene Corporation
691,344 open positions
Centene Corporation is a Fortune 100 healthcare innovator that blends data analytics, cloud computing, and AI to deliver personalized care across the United States. With a mission to increase access to quality health services, Centene invests heavily in digital platforms, electronic health records, and telehealth solutions that support millions of members.
Tech talent at Centene finds roles ranging from full‑stack software engineers and cloud architects to data scientists, cybersecurity analysts, and product managers. The company also hires UX/UI designers, DevOps specialists, and compliance officers who help build secure, scalable health IT systems that meet HIPAA and industry standards.
By browsing Centene’s listings on Job Transparency, candidates gain instant access to benchmarked salary ranges, real‑time employee reviews, and skill demand insights. This data helps you negotiate better offers, gauge company culture, and target positions that align with your career goals.
Sr. Cisco Nexus Dashboard Fabric Controller Engineer
Company: Arganteal Corporation
Location: Chicago, IL
Posted Apr 13, 2024
The job posting is for a highly skilled Cisco Nexus Dashboard Fabric Controller Senior Engineer to work remotely for 5 months with potential extension. The role involves designing, deploying, and managing Cisco Nexus Dashboard Fabric Controller environments, developing automation tools, providing technical leadership, monitoring network performance, collaborating with IT teams, and staying updated with network technologies. The ideal candidate should have a Bachelor's degree in Computer Science or related field, at least 5 years of network engineering experience with a focus on Cisco data center technologies, expertise in managing Cisco Nexus Dashboard Fabric Controller, understanding of Cisco ACI and Nexus series switches, proficiency in network automation and scripting languages, strong problem-solving skills, and excellent communication and project management skills.
Senior Customer Service Representative
Company: Harsco Corporation
Location: Birmingham, AL
Posted Apr 12, 2024
Clean Earth is a leading specialty waste company in the US, offering comprehensive solutions for contaminated soil, dredged material, and hazardous/non-hazardous waste. They provide recycling, disposal, and beneficial reuse services, catering to various industries. The company is known for its one-source, full-service solution, detailed processes, and exceptional customer service. They are currently seeking a Customer Service Representative with strong attention to detail, customer service acumen, and business acumen. The role involves managing customer needs, coordinating waste disposal, and increasing revenue growth. The ideal candidate should be proficient in Microsoft Office and CRM systems, with excellent communication skills.
Systems Engineer/Integrator
Company: Diné Development Corporation
Location: Dayton, OH
Posted Apr 12, 2024
Dine Source is seeking a Systems Engineer/Integrator with a bachelor's degree in IT, 4+ years of experience, and the ability to obtain a Secret security clearance. The role involves planning and designing systems infrastructure, analyzing and maintaining systems, and ensuring they meet requirements. Familiarity with data analytics, open-source tools, cloud computing, machine learning, and data visualization is required. The company adheres to anti-discrimination regulations.
Regional Account Manager
Company: Harsco Corporation
Location: Birmingham, AL
Posted Apr 12, 2024
Clean Earth is a leading waste management company providing remediation, disposal, recycling, and beneficial reuse solutions. The company is seeking a Regional Account Manager to expand its business within pre-assigned territories.
118 Software Engineer 1
Company: ARSIEM Corporation
Location: Baltimore, MD
Posted Apr 13, 2024
ARSIEM Corporation is a trusted partner to US Government agencies, offering a career with growth opportunities and impact. They are currently hiring a Software Engineer for a position in Annapolis Junction, MD. The role involves developing, maintaining, and enhancing complex software systems. Minimum qualifications include 7 years of SWE experience and a Bachelor's degree in Computer Science. Preferred qualifications include experience in software design, debugging, and process improvement. The position requires an active TS/SCI clearance and US Citizenship.
Senior Accountant
Company: Rogers Corporation
Location: Phoenix – Mesa – Scottsdale, AZ
Posted Apr 12, 2024
The role is responsible for ensuring accurate financial reporting and providing strategic guidance. The job requires strong analytical and problem-solving skills, as well as proficiency in financial management software and accounting principles.
EHS Specialist
Company: Dover Corporation
Location: Other US Location
Posted Apr 12, 2024
Dover Food Retail (DFR) is a leading manufacturer of various food retail products and services, part of the Refrigeration and Food Equipment segment of the Dover Corporation. DFR is known for its innovative glass doors and merchandising technologies under brands like HillPhoenix and Anthony. The company values creativity, customer-centric innovation, and responsible relationships with customers. DFR is currently seeking an Environmental Health & Safety (EHS) Specialist in Centerville, Iowa. The role involves partnering with the operations team to drive safety, conducting incident investigations, and ensuring compliance with EHS regulations. The ideal candidate should have a bachelor's degree in a relevant field or an Associate Degree with a relevant EHS Professional Certification, along with 1-3 years of EHS experience. Preferred qualifications include strong interpersonal skills, Microsoft Word and Excel proficiency, and experience in a fast-paced manufacturing environment.
Product Owner, eCommerce - Hybrid
Company: Carnival Corporation
Location: Miami, FL
Posted Apr 13, 2024
Princess Cruises is seeking an eCommerce Product Owner for a hybrid role based in Fort Lauderdale. The ideal candidate will have 1-3+ years of product management experience, preferably in travel, hospitality, entertainment, or packaged goods. Responsibilities include creating and maintaining the product backlog, providing vision and direction to the development team, and driving product enhancements. Benefits include cruise and travel privileges, health benefits, 401(k), employee stock purchase plan, training, tuition reimbursement, rewards, and a base salary range of $84,700.00 to $114,400.00.
414 System Administrator 3
Company: ARSIEM Corporation
Location: Baltimore, MD
Posted Apr 13, 2024
ARSIEM Corporation is a trusted partner to US Government agencies, offering reliable technical solutions and a career with growth opportunities. They are currently hiring a System Administrator for a position in Annapolis Junction, MD, with a $40,000 bonus incentive. The role involves supporting IT systems, managing infrastructure, and providing Tier 1 and 2 problem resolution. Minimum qualifications include 15 years of SA experience, a bachelor's degree, and DoD 8570 compliance with IAT Level III or higher. Preferred qualifications include experience with UNIX and Windows operating systems, and understanding of SOA.
Lien Specialist I
Company: CorVel Corporation
Location: Greater LA Area
Posted Apr 13, 2024
The Lien Specialist role involves collaborating with Claims Adjusters and Managers to expedite claim file closures. Key responsibilities include negotiating and resolving medical treatment liens, preparing legal documents, and attending WCAB hearings. The role requires excellent communication skills, problem-solving abilities, and proficiency in MS Office. A high school diploma and at least 3 years of industry experience are preferred. CorVel, a certified Great Place to Work® Company, offers a competitive pay range of $22.10 - $32.98 per hour and a comprehensive benefits package.
Vice President, Regulatory Operational Excellence
Company: IMVT Corporation
Location: USA
Posted Apr 12, 2024
<p><strong> <strong><p> <p><strong>Organizational Overview<strong><p> <p>Immunovant is a clinicalstage biopharmaceutical company with a company vision focused on enabling normal lives for patients with autoimmune diseases Our lead asset IMVT1401 is a novel fullyhuman antiFcRn monoclonal antibody in clinical development for multiple indications delivered as a subcutaneous injection for the treatment of autoimmune diseases mediated by pathogenic IgG antibodies Immunovant is committed to developing innovative therapies that not only treat the symptoms but modify the course of autoimmune diseases while restoring hope and health to patients with autoimmune disease by developing and delivering highvalue restorative therapies that enable them to live normal lives<p> <p> <p> <p><strong>The Role<strong><p> <p>This newly created role within the Regulatory Affairs organization is an exciting opportunity for a seasoned Regulatory Affairs professional to serve as a leader in the oversight and optimization of multiple groups within the Regulatory Affairs department The VP of Regulatory Affairs Operational Excellence reports to the Senior Vice President of Regulatory Affairs and will be responsible for overseeing the following Regulatory groups<p> <ul style=> <li style=>Regulatory Operations <ul style=> <li style=>Regulatory Operations is responsible for regulatorysubmission coordination incl development of submission content plans and timelines regulatory information management and regulatory submissions business processes related to submission publishing standards and correspondence archival and Veeva RIM utilization and RIMSMART<li> <ul> <li> <li style=>Regulatory Business Operations <ul style=> <li style=>Regulatory Business Operations is responsible for development of best practices for information sharing and document writing vendor management including regulatory consultants subscriptions and contract medical writers assessment of new technologies to improve efficiency in endtoend regulatory support of clinical development programs and developmentassessment of overall regulatory and medical writing department budgets<li> <ul> <li> <li style=>Medical Writing <ul style=> <li style=>Immunovant Medical Writing is composed of both inhouse and contract writers The team is responsible for development of writing standards and best practices writing of documents including briefing documents clinical protocols CTD modules investigators brochures clinical study reports responses to Health Authority queries etc<li> <ul> <li> <ul> <p>The ideal candidate will have subject matter knowledge in the above Regulatory arenas SHe should have a proven track record of managing multiple functions and people with the discretion to appropriately prioritize initiatives and needs of their teams groups and individuals in a fastpaced and dynamic environment This position will need to have strong relationships across all functions associated with document content writing management and retention requirements This position will drive operational transformation to accommodate near and longterm corporate objectives that require Regulatory operational foresight SHe will review clinicalregulatory documents to support all phases of drug development by leading MW project management activities of an interdisciplinary team to ensure documents are strategic high quality and comply with internal and external standards SHe will delegate workplans for ongoing initiatives as appropriate and provide leadership and strategic support for the team responsible for development and implementation<p> <p> <p> <p><strong>Key Responsibilities <strong><p> <ul style=> <li style=>Manage for 3 to 6 Regulatory personnel including the Senior Director heads of Regulatory Operations and Medical Writing who will also have their own direct reports<li> <li style=>Manage budget for Medical Writing and Regulatory Affairs department<li> <li style=>Manage short term and long term activities and initiatives of Regulatory Operations Regulatory Business Operations and Medical Writing while adapting to changing priorities of the company and overall portfolio of programs<li> <li style=>Development and rollout of document templates and writing standards to ensure compliance with regulations GxP standards and other internalexternal guidelines<li> <li style=>Portfoliolevel oversight to ensure key content messaging messaging in regulatoryclinical documents across 1401 and 1402 programs<li> <li style=>Drive organizational improvement by proactively communicating with Regulatory and crossfunctional stakeholders to problemsolve and identify appropriate operating models for each of the relevant functions<li> <li style=>Serve as a conduit of information flow between Regulatory leadership and the functions overseen by this position Identify opportunities for synergies across the Regulatory organization<li> <li style=>Present various topics and recommendations to Immunovant executive leadership<li> <li style=>Ensure teams are tracking towards timely completion of deliverables<li> <li style=>When necessary serve as intermediary between vendors in support of Immunovant Regulatory staff<li> <li style=>Assess and communicate regulatory requirements to ensure all development activities are in compliance with applicable regulations and guidelines<li> <li style=>Continually evaluate appropriateness and effectiveness of quality standards templates information technology platforms and processes identify opportunities for improvements<li> <li style=>Foster the growth and development and provide mentorship for the Regulatory Affairs team<li> <ul> <p><strong> <strong><p> <p><strong>Requirements<strong><p> <ul style=> <li style=>Bachelors degree in a scientific discipline required advanced degree highly desired<li> <li style=>Minimum 1215 years regulatory industry experience in biopharmaceuticals<li> <li style=>Experience with Veeva and implementation of new processes within Veeva<li> <li style=>Experience with management of a budget to facilitate fiscal planning and accountability of spending<li> <li style=>Handson or oversight experience with regulatory support of clinical trials regulatory operations and submission management and regulatory writing<li> <li style=>Experience with clinical stage assets required experience with BLAMAA and postmarketing strongly preferred<li> <li style=>Highly effective communication skills and confidence to lead strongly when necessaryappropriate<li> <li style=>Ability to pivot comfortably and judiciously communicate change within a rapidly evolving company environment<li> <li style=>Understanding of policy laws regulations and guidelines as they apply to Regulatory Agencies for drug development and approval<li> <li style=>Strong knowledge of eCTD elements and structure with regulatory writing skills<li> <li style=>Strong knowledge of drug development FDA EMA and other guidelines and regulations<li> <li style=>Working knowledge of electronic submission procedures and document management system requirements<li> <li style=>Working knowledge of regulatory submission management electronic publishing and document management Experience with Veeva systems strongly preferred<li> <li style=>Experience of filing NDABLAMAA application and meeting submission quality and standards<li> <li style=>Demonstrated experience with effective management of direct reports contractorsconsultants and vendors<li> <ul> <p> <p> <p><strong>Work Environment<strong><p> <ul style=> <li style=>Dynamic interactive fastpaced and entrepreneurial environment<li> <li style=>Immunovants headquarters is located in New York City The position will be remote work<li> <li style=>Domestic travel required up to 20<li> <ul> <p> <p> <p>Compensation is based on a number of factors including market location and may vary depending on jobrelated knowledge skills and experience Equity signon bonuses and other forms of compensation may be provided as part of a total compensation package in addition to a full range of medical dental vision 401k and other benefits including unlimited paid time off and parental leave The annual base salary for this position ranges from $32000000 $34000000<p> <p> <p> <p> <p><img src=httpsremotivecomjobtrack1906512blankgifsource=publicapi alt=>
Sr. IT Financial Analyst
Company: Carnival Corporation
Location: Miami, FL
Posted Apr 13, 2024
The job description is for a Senior IT Financial Analyst position at Carnival Cruise Line. The role involves managing IT financials, providing financial planning and analysis, and working with IT leaders and other departments. The job requires a bachelor's degree in finance, accounting, or a related field, and 5+ years of experience in finance and accounting.