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assistant case coordinator– health/community network Jobs in Irvine

associate, clinical research Jobs in Irvine

associate, clinical research

clinical research coordinator Jobs in Irvine

clinical research coordinator

clinical scribe

investment research associate Jobs in Irvine

investment research associate

associate clinical research

JenaValve Technology, Inc.

<div>
 
 Job Title:
 
 Associate, Clinical Research
 
 
 
 Role Level:
 
 Individual Contributor (IC)
 
 
 
 Supervisor/Manager Title:
 
 Director, Clinical Affairs
 
 
 
 Job Location &amp; Environment:
 
 Irvine, CA, Corporate Office
 
 
 
 Job Description Summary:
 
 The Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market and or post-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable regulations.
 
 
 
 Job Responsibilities
 
 
 
 <ul>
 <li>
 Support site management and interact with site coordinators, investigators, and field monitors in collecting data and resolving queries to meet the protocol requirements in a timely manner.
 </li>
 <li>
 Ensure quality data management activities &ndash; i.e., data review, query generation and resolution. Generate status reports to clinical staff and management.
 </li>
 <li>
 Maintain Trial Master Files and trackers for clinical trials.
 </li>
 <li>
 Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current.
 </li>
 <li>
 Conduct periodic audits of internal files to ensure compliance per site Institutional Review Board (IRB) and/or Ethics Committee (EC) policy (i.e. IRB continuing review approval period and expiration dates).
 </li>
 <li>
 Provide clinical operational support during preparation for and conduct of all clinical audits and inspections.
 </li>
 <li>
 Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives.
 </li>
 <li>
 Partner with management to manage external vendors, including ongoing supplier qualification.
 </li>
 <li>
 Assist field clinical monitors in preparation for site training and monitoring visits
 </li>
 <li>
 Support monitoring of sites on an as-needed basis.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 Required Education and Experience:
 
 
 
 <ul>
 <li>
 At least 1 year of experience in clinical trial research is required (preferred in medical devices).
 </li>
 <li>
 Advanced degree in a biological science / pharmacy/ nursing desired.
 
 
 </li>
 </ul>
 
 Skills And Abilities Required For This Job
 
 
 
 <ul>
 <li>
 Proficient in clinical trial management and electronic data capture systems to document and record information.
 </li>
 <li>
 Excellent communication skills (written and verbal English) so as to be able to build effective relationships with trial center staff and colleagues.
 </li>
 <li>
 Some knowledge of GCPs governing the conduct of clinical trials, Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines.
 </li>
 <li>
 Very organized and able to pay close attention to detail.
 </li>
 <li>
 Team player with a willingness to help where needed and work with diverse people.
 
 
 </li>
 </ul>
 
 Physical Requirements
 
 
 
 <ul>
 <li>
 Ability to travel up to 20% time.
 </li>
 </ul>
</div>

Associate, Clinical Research

Kelly Science, Engineering, Technology & Telecom

<div>
 
 Kelly Science and Clinical FSP is currently seeking a
 
 Study Start Up Specialist
 
 for a long-term engagement in the US with one of our Global Medical Device clients in Irvine, California. This is a
 
 hybrid
 
 position on site
 
 Tuesday/Thursday and every other Friday.
 
 This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
 
 
 
 
 
 Fraudulent Applications: All information provided during the application process will be verified. Misrepresentation of credentials, identity fraud, or use of proxy interviewers will result in immediate disqualification and may be reported to appropriate authorities.
 
 
 
 
 
 
 DESCRIPTION
 
 
 
 
 
 <ul>
 <li>
 Participates in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures;
 </li>
 <li>
 May serve as the primary contact for clinical trial sites (e.g. site management);
 </li>
 <li>
 Assists in the development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports);
 </li>
 <li>
 Supports applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed;
 </li>
 <li>
 Coordinates and executes ordering, tracking, and accountability of investigational devices and trial materials;
 </li>
 <li>
 Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel;
 </li>
 <li>
 Interfaces and collaborates with Clinical Research Associates (CRAs);
 </li>
 <li>
 Assists in overseeing and supports the development and execution of Investigator agreements and trial payments;
 </li>
 <li>
 Assists in clinical data review to prepare data for statistical analyses and publications;
 </li>
 <li>
 May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need;
 </li>
 <li>
 May provide on-site procedural protocol compliance and data collection support to the clinical trial sites;
 </li>
 <li>
 Assists in tracking assigned project budgets;
 </li>
 <li>
 May perform other duties assigned as needed;
 </li>
 <li>
 Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders;
 </li>
 <li>
 Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures;
 </li>
 <li>
 Should develop a strong understanding of the pipeline, product portfolio and business needs;
 </li>
 <li>
 Generally manages work with supervision. Independent decision-making for simple situations but requires guidance for complex situations.
 </li>
 </ul>
 
 
 
 
 
 EXPERIENCE AND EDUCATION
 
 
 
 
 
 Education
 
 
 
 <ul>
 <li>
 Minimum of a Bachelor&rsquo;s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.
 </li>
 </ul>
 
 
 
 Experience
 
 
 
 <ul>
 <li>
 BS with at least 2 years, MS and PhD with at least 1 year of relevant experience preferred.
 </li>
 <li>
 Previous experience in clinical research or equivalent is desired.
 </li>
 <li>
 Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV,&hellip;).
 </li>
 <li>
 Clinical/medical background is a plus.
 </li>
 <li>
 Medical device experience is a plus.
 </li>
 </ul>
 
 
 
 
 
 REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS
 
 
 
 
 
 Functional and Technical Competencies:
 
 
 
 <ul>
 <li>
 Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations;
 </li>
 <li>
 Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations;
 </li>
 <li>
 Presentation and technical writing skills;
 </li>
 <li>
 Written and oral English communication skills.
 </li>
 </ul>
 
 
 
 
 
 
 
 
 
 Leadership Competencies:
 
 
 
 
 Leadership required in alignment with J&amp;J Leadership Imperatives:
 
 <ul>
 <li>
 
 Connect
 
 - Develop collaborative relationships with key internal and external stakeholders.
 </li>
 <li>
 
 Shape
 
 - Actively participate in departmental process improvement activities.
 </li>
 <li>
 
 Lead
 
 - Take ownership in critical scientific thinking and development of self and engage in transparent and constructive conversations.
 </li>
 <li>
 
 Deliver
 
 - Strive to ensure all deliverables on allocated studies are met on time, within budget and in compliance to SOPs and regulations.
 </li>
 </ul>
 
 
 
 
 
 TRAVEL REQUIREMENTS
 
 
 <ul>
 <li>
 Ability to travel approximately 20% depending on the phase of the program.
 </li>
 </ul>
 
 
 
 
 
 EXTERNAL INTERACTIONS
 
 
 <ul>
 <li>
 Frequent (several times per month) interaction with physicians and research staff at centers selected for involvement in clinical research as well as those being evaluated.
 </li>
 <li>
 May have regular interaction with third party vendors supporting clinical studies as applicable per clinical trial.
 </li>
 </ul>
 
 
</div>

Study Start Up Specialist

Johnson & Johnson

<div>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com
As guided by Our Credo, Johnson &amp; Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson &amp; Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Discovery &amp; Pre-Clinical/Clinical Development
Job Sub Function:
Clinical Development &amp; Research &ndash; Non-MD
Job Category:
Scientific/Technology
All Job Posting Locations:
Irvine, California, United States of America
Job Description:
Johnson &amp; Johnson MedTech Electrophysiology is recruiting for a Senior Clinical Research Specialist, (Clinical Operations Start-up) to support the Electrophysiology (EP) business unit based in Irvine, CA.
At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we&rsquo;re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that&rsquo;s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech.
Summary:
The Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&amp;D Department while fostering strong, productive relationships with colleagues across the organization.
Duties &amp; Responsibilities:
Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson &amp; Johnson, procedures and guidelines, this position:<ul><li>
Serves as a Senior Clinical Research Specialist within the Clinical R&amp;D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for J&amp;J MedTech Electrophysiology</li></ul><ul><li>
Oversees/executes feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures</li><li>
May serve as the primary contact for clinical trial sites (e.g. site management)</li><li>
Contributes towards development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports,&hellip;.)</li><li>
Supports applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed</li><li>
Manages/oversees ordering, tracking, and accountability of investigational devices and trial materials</li><li>
Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel</li><li>
Interfaces, collaborates and oversees Clinical Research Associates (CRAs)</li><li>
Oversees and supports the development and execution of Investigator agreements and trial payments</li><li>
Is responsible for clinical data review to prepare data for statistical analyses and publications</li><li>
May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need</li><li>
May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) within the assigned projects</li><li>
May provide on-site procedural protocol compliance and data collection support to the clinical trial sites</li><li>
Contributes to the critical assessment of the literature and to the interpretations and disseminations of all evidence generated</li><li>
Contributes to delivery of assigned clinical projects, through effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs)</li><li>
May assist with the development of e Post-Market Clinical Follow-up (PMCF) Plans and PMCF</li><li>
Evaluation Reports (ER) within the defined timelines and review/update at planned intervals</li><li>
May assist with maintaining the overview to assure (study) commitments are timely and properly met by coordination of specific documentation and contribution to cross-functional review of associated documents where relevant</li><li>
Supports project/study budget activities</li><li>
Mentors team members</li><li>
May perform other duties assigned as needed</li><li>
Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders</li><li>
Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures</li><li>
Should develop a strong understanding of the pipeline, product portfolio and business needs</li><li>
Generally manages work with supervision, dependent on project complexity. Independent decision-making for simple and more advanced situations but requires guidance for complex situations.</li></ul>
Experience and Education:<ul><li>
Minimum of a Bachelor&rsquo;s Degree preferably in Life Science, Physical Science, Nursing, or</li></ul><ul><li>
Biological Science required.</li><li>
BS with at least 4 years, MS with at least 3 years, PhD with at least 2 years of relevant</li><li>
experience preferred.</li><li>
Previous experience in clinical research or equivalent is required.</li><li>
Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO</li><li>
14155, MDR, MEDDEV,&hellip;).</li><li>
Clinical/medical background is a plus.</li><li>
Medical device experience is highly preferred.</li></ul>
Functional and Technical Competencies:<ul><li>
Good understanding of clinical research science and processes, clinical trends, and global</li></ul><ul><li>
clinical trial regulations</li><li>
Proven track record in supporting delivery of clinical projects within clinical/ surgical research setting, on time, within budget and in compliance to SOPs and regulations</li><li>
Good presentation and technical writing skills;</li><li>
Good written and oral English communication skills;</li><li>
Leadership Competencies:</li><li>
Ability to lead small study teams to deliver critical milestones, as may be assigned.</li><li>
Leadership required in alignment with J&amp;J Leadership Imperatives</li><li>
Connect - Develop collaborative relationships with key internal and external stakeholders.</li><li>
Shape - Make recommendations for and actively participate in departmental process improvement activities.</li><li>
Lead - Take ownership in critical scientific thinking and development of self and engage in transparent and constructive conversations.</li><li>
Deliver - Strive to ensure all deliverables on allocated studies are met on time, within budget and in compliance to SOPs and regulations.</li></ul>
Johnson &amp; Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson &amp; Johnson is committed to providing an interview process that is inclusive of our applicants&rsquo; needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
#LI-Hybrid
Required Skills:
Preferred Skills:
Analytical Reasoning, Clinical Data Management, Clinical Evaluations, Clinical Trial Protocols, Coaching, Consulting, Data Savvy, Drug Discovery Development, Good Clinical Practice (GCP), Medicines and Device Development and Regulation, Persistence and Tenacity, Regulatory Affairs Management, Research Documents, Resource Management, Safety-Oriented, Scientific Research, Technologically Savvy
The anticipated base pay range for this position is :
$92,000.00 - $148,350.00
Additional Description for Pay Transparency:
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: 
 
Vacation &ndash;120 hours per calendar year 
 
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado &ndash;48 hours per calendar year; for employees who reside in the State of Washington &ndash;56 hours per calendar year 
 
Holiday pay, including Floating Holidays &ndash;13 days per calendar year 
 
Work, Personal and Family Time - up to 40 hours per calendar year 
 
Parental Leave &ndash; 480 hours within one year of the birth/adoption/foster care of a child 
 
Bereavement Leave &ndash; 240 hours for an immediate family member: 40 hours for an extended family member per calendar year 
 
Caregiver Leave &ndash; 80 hours in a 52-week rolling period10 days 
 
Volunteer Leave &ndash; 32 hours per calendar year 
 
Military Spouse Time-Off &ndash; 80 hours per calendar year 
 
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
Johnson &amp; Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson &amp; Johnson is committed to providing an interview process that is inclusive of our applicants&rsquo; needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.
#LI-Hybrid</div>

Sr. Clinical Research Specialist, (Clinical Operations Start-up)

MaximaTek

<div>
 
 
 About the Company
 
 
 
 We are seeking a detail-oriented and motivated Clinical Research Coordinator (CRC) to support the planning, execution, and management of clinical trials. This role is ideal for candidates with foundational to intermediate experience in clinical research who are looking to grow their careers in a fast-paced, compliance-driven environment. The CRC will work closely with investigators, sponsors, and study participants to ensure trials are conducted ethically, efficiently, and in accordance with regulatory guidelines.
 
 
 
 
 
 
 About the Role
 
 
 
 This role is ideal for candidates with foundational to intermediate experience in clinical research who are looking to grow their careers in a fast-paced, compliance-driven environment.
 
 
 
 
 
 
 Responsibilities
 
 
 <ul>
 <li>
 Coordinate and manage day-to-day clinical trial activities from study start-up to close-out
 </li>
 <li>
 Screen, recruit, and enroll study participants according to protocol criteria
 </li>
 <li>
 Obtain informed consent and ensure participant understanding of study procedures
 </li>
 <li>
 Schedule and conduct study visits, including data and sample collection
 </li>
 <li>
 Maintain accurate and up-to-date study documentation, including source documents and case report forms (CRFs)
 </li>
 <li>
 Ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and institutional policies
 </li>
 <li>
 Communicate effectively with investigators, sponsors, and clinical trial stakeholders
 </li>
 <li>
 Track and report adverse events and protocol deviations
 </li>
 <li>
 Assist with monitoring visits, audits, and regulatory inspections
 </li>
 <li>
 Manage study supplies, investigational products, and lab samples
 </li>
 <li>
 Support Institutional Review Board (IRB)/Ethics Committee submissions and correspondence
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Life Sciences, Nursing, Pharmacy, Public Health, or a related field
 </li>
 </ul>
 
 
 
 
 
 Required Skills
 
 
 <ul>
 <li>
 Knowledge of clinical trial processes and regulatory requirements (GCP, ICH guidelines)
 </li>
 <li>
 Strong organizational and time management skills
 </li>
 <li>
 Attention to detail and accuracy in documentation
 </li>
 <li>
 Excellent interpersonal and communication skills
 </li>
 <li>
 Ability to work independently and as part of a multidisciplinary team
 </li>
 <li>
 Proficiency in Microsoft Office and clinical trial management systems (CTMS) or electronic data capture (EDC) systems
 </li>
 </ul>
 
 
 
 
 
 Preferred Skills
 
 
 <ul>
 <li>
 Certification such as ACRP-CP, CCRC, or equivalent
 </li>
 <li>
 Experience with multiple therapeutic areas or phases of clinical trials
 </li>
 <li>
 Familiarity with regulatory submissions and audit processes
 </li>
 </ul>
 
 
 
 
 Ready to Take the Next Step? Email your updated resume to: shivani@maximatek.com
 
 
 
</div>

Clinical Research Coordinator

Sunflower Bank

<div>At Sunflower Bank, N.A., we&rsquo;re experiencing great growth. Since our founding in 1892, we've been committed to serving our communities and supporting the team members who make it all possible. As a full-service financial institution, we offer a full range of relationship-focused services to meet personal, business, and wealth-management financial objectives. Creating Possibility is not just our mission, it&rsquo;s what we do every day for clients and associates. Learn more about Sunflower Bank, N.A. at sunflowerbank.com.
Sunflower Bank, N.A./First Foundation Advisors is looking for an energetic, highly motivated individual to fill the position of a full-time Investment Research Associate at our Irvine, CA location.
The salary range for this position is $60,100 to $84,500 depending on knowledge, skills, abilities, experience, and location.
Summary:
The Investment Research Analyst will be primarily responsible for assisting the Investment Committee members in ad hoc efforts including reporting, manager due diligence and streamlining workflow processes for both public and private, as well as proprietary &amp; non-proprietary, investment solutions. The associate will also support the advising team by responding to questions and requests about securities on the firm&rsquo;s investment platform from client-facing teams.
Primary Responsibilities<ul><li>
Support investment strategists in performing manager due diligence reporting, including those for non-proprietary and proprietary investments, separately managed accounts, mutual funds, exchange-traded funds, and alternative investments.</li><li>
Ensure knowledge of entire investment solution suite; recommend investment solutions to Portfolio Strategist and Wealth Advisors for client use based upon clients' needs and constraints.</li><li>
Strategize with investment team in updating asset class outlook and asset allocation.</li><li>
Respond to inquiries about the investment platform from business development team members.</li><li>
Maintain updated fund manager collateral for easy access by Relationship Managers and Wealth Advisors.</li><li>
Serve as a liaison for communications between Investment Strategists and fund manager partners.</li><li>
Perform ad hoc analysis on portfolios and investment strategies.</li><li>
Coordinate duties between Investment Strategists and Operations for investments.</li><li>
Conduct research and analysis to support the investment sub-committee&rsquo;s theses or find potential opportunities.</li><li>
Adheres to compliance programs and completes required training on time.</li><li>
Understands and complies with requirements of all laws and regulations applicable to position.</li><li>
Perform the job in accordance with applicable industry laws and regulations as well as the policies and procedures established by the company.</li><li>
Responsible for upholding Fair and Responsible Banking practices and Code of Ethics and Conduct guidelines.</li><li>
Understand and participate in the Bank&rsquo;s Community Reinvestment Act program.</li><li>
Perform other duties as assigned.</li></ul>
Education / Experience<ul><li>
Bachelor&rsquo;s Degree in Finance, Economics, Physical Sciences, Engineering, or Computer Science is preferred.</li><li>
3-5 Years of investment industry experience preferred.</li><li>
Knowledge of valuing financial instruments, including those in Equity and Fixed Income.</li><li>
Bloomberg, FactSet, Argus and/or Morningstar experience preferred.</li><li>
Willingness to pursue CFA and/or CAIA designation a plus.</li><li>
Experience with Python/AI workflow automation or demonstrated aptitude and eagerness to learn.</li><li>
Prior or current involvement in investment-related undergraduate clubs or community involvement a plus.</li><li>
Possesses a deep quantitative and analytical mindset.</li><li>
Advanced proficiency with Excel &amp; PowerPoint. VBA and/or financial modeling skills a plus.</li><li>
A team player with excellent communication skills who exhibits a high level of professionalism.</li><li>
Strong organizational skills and initiative with systematic follow-up &amp; a focus on accuracy and reliability.</li><li>
Must be bondable.</li></ul>
Working Conditions:
The physical demands of this position require the ability to perform essential job functions with or without reasonable accommodation. Employees may spend extended periods sitting or standing, using hands to operate computers or other equipment, and reaching for work-related tasks. Regular walking may be required, along with occasional bending, stooping, kneeling, or climbing. The role may involve lifting or moving items weighing up to 10 pounds. Vision requirements include close and distance vision, color and peripheral vision, depth perception, and the ability to adjust focus.
Sunflower Bank Benefits
People choose to &ldquo;bank&rdquo; with us, but for those we serve, we&rsquo;re more than a bank. We strive to be the financial backbone of their lives, and we know that starts with our team.
Our supportive culture empowers team members to grow and seize new opportunities. Like our namesake, the sunflower, we are:<ul><li>
Rooted in Strength</li><li>
Propelled by Growth</li><li>
Individuals in a Great Whole</li><li>
Creating Possibility</li><li>
Community Focused</li></ul>
Associates enjoy outstanding benefits, including:<ul><li>
401(k) Plan with 6% Match</li><li>
Health/Dental/Vision Insurance</li><li>
Company-paid Life Insurance</li><li>
Tuition Reimbursement</li><li>
Fitness Reimbursement</li><li>
Paid Time Off</li><li>
Volunteer Leave</li><li>
Paid Holidays</li><li>
Plus many more associate perks &amp; incentives!</li></ul>
If you qualify, apply online at www.sunflowerbank.com/careers.
You&rsquo;ve never worked anyplace like Sunflower Bank!
EOE/AA: Minorities/Females/Disabled/Vets
Sunflower Bank, N.A. is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, status as a qualified individual with a disability, sexual orientation, gender identity, or any other characteristic protected by law.
Open until filled; early application encouraged. This vacancy announcement may be used to fill similar positions within 90 days.
If you are a California resident, you may be entitled to certain rights regarding your personal information, which is information that identifies, relates to, or could reasonably be linked with a particular California resident or household. Additional information about our data collection practices and location-specific notices is available on our privacy policy.</div>

Investment Research Associate

NeurOptics

<div>
 
 
 About NeurOptics
 
 
 
 NeurOptics is the global leader in the science of pupillometry, advancing neurological patient care through clinically validated, data-driven technology. Driven by a passion to improve patient outcomes, NeurOptics&rsquo; solutions are used across critical care nursing, neurology, neurosurgery, emergency medicine, and critical care medicine to inform high-stakes clinical decision-making.
 
 
 Headquartered in Irvine, California, NeurOptics operates globally with representation in more than 50 countries.
 
 
 At NeurOptics, we are passionate patient advocates. Improving neurological patient outcomes is our life&rsquo;s work.
 
 
 
 
 
 
 Role Overview
 
 
 
 The
 
 Product Manager
 
 is a key contributor within NeurOptics&rsquo; Sales and Marketing organization, responsible for
 
 owning and executing product marketing strategy
 
 for the company&rsquo;s neuroscience and pupillometry product portfolio.
 
 
 This is a
 
 high-visibility role
 
 requiring strong product judgment, clinical understanding, and cross-functional leadership. The Product Manager translates market, customer, and clinical insights into differentiated positioning, effective commercialization strategies, and sustained market expansion across U.S. and international markets.
 
 
 This position is based on site at NeurOptics&rsquo; Corporate Headquarters in Irvine, California.
 
 
 
 
 
 
 Professional Development
 
 
 
 NeurOptics is deeply committed to continuous learning and professional growth. The Product Manager will complete structured onboarding focused on clinical immersion, portfolio knowledge, and internal process alignment. Ongoing development opportunities support advancement in product leadership, strategic thinking, and cross-functional influence throughout tenure at NeurOptics.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 Product &amp; Portfolio Leadership
 
 
 <ul>
 <li>
 Own and execute downstream product management strategy for neuroscience and pupillometry products, aligned with corporate objectives and the Sales Game Plan
 </li>
 <li>
 Lead product pre-launch, launch, and post-launch execution for next-generation NPi Pupillometry solutions, including medical devices and data integration products
 </li>
 <li>
 Translate product strategy into clear positioning, pricing strategy, promotional initiatives, and market execution plans
 </li>
 </ul>
 
 
 Market Strategy &amp; Customer Insights
 
 
 <ul>
 <li>
 Define market and customer requirements for current and future products through primary research, customer engagement, field presence, and scientific conferences
 </li>
 <li>
 Conduct onsite field work with customers to understand clinical workflows, adoption barriers, and value drivers
 </li>
 <li>
 Monitor competitive, clinical, and healthcare market developments that may impact product or portfolio strategy
 </li>
 </ul>
 
 
 Sales Enablement &amp; Global Commercial Support
 
 
 <ul>
 <li>
 Serve as a product subject matter expert, delivering product training, messaging, and strategic support to global sales and distribution teams
 </li>
 <li>
 Develop and deliver marketing communications and presentations to U.S. and international distribution partners aligned with key marketing initiatives and sales priorities
 </li>
 <li>
 Partner with Sales leadership to support strategic accounts, customer meetings, and market expansion initiatives
 </li>
 <li>
 Manages Marketing vendors, software and technologies, including identification and implementation of new platforms and processes
 </li>
 </ul>
 
 
 Cross-Functional Leadership
 
 
 <ul>
 <li>
 Lead product-specific core teams in a hub-and-spoke model, coordinating efforts across Sales, Clinical Education, Customer Service, Operations, Regulatory, and other stakeholders
 </li>
 <li>
 Collaborate with Regulatory Affairs to ensure appropriate alignment of product claims and marketing materials
 </li>
 <li>
 Work closely with Customer Service and Clinical teams to ensure service readiness, education, and ongoing support excellence
 </li>
 </ul>
 
 
 Forecasting, Analytics &amp; Execution
 
 
 <ul>
 <li>
 Develop and maintain sales forecasts for assigned product lines; communicate insights to Marketing, Sales Management, and Operations
 </li>
 <li>
 Leverage CRM and commercial data to identify trends, opportunities, and risks related to adoption and growth.
 </li>
 <li>
 Manage and update CRM design and functionality in conjunction with Marketing, Sales Management, Customer Service, Operations, Finance, and other stakeholders
 </li>
 <li>
 Support continuous improvement in commercialization effectiveness and execution
 </li>
 </ul>
 
 
 Field &amp; Industry Engagement
 
 
 <ul>
 <li>
 Travel with sales and clinical education teams to support sales acceleration, gather market intelligence, and strengthen customer relationships
 </li>
 <li>
 Represent NeurOptics professionally at industry conferences, customer meetings, and scientific forums
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Marketing, Business, Biological/Clinical Science, Engineering, or related field
 </li>
 <li>
 MBA preferred
 </li>
 <li>
 5+ years of medical device or healthcare product management or product marketing experience; sales experience a plus
 </li>
 <li>
 Demonstrated experience supporting hospital-based products and familiarity with neuroscience or critical care clinical environments
 </li>
 <li>
 Strong track record of supporting product launches, portfolio growth, and cross-functional initiatives in regulated environments
 </li>
 <li>
 Excellent communication and presentation skills with the ability to influence internal and external stakeholders
 </li>
 <li>
 Strong analytical, financial, and problem-solving skills
 </li>
 <li>
 Proven ability to convert customer and product feedback into actionable marketing and commercialization strategies
 </li>
 <li>
 Highly self-directed, with the ability to manage multiple initiatives and shifting priorities
 </li>
 <li>
 Proficient in Microsoft 365 (Word, Excel, PowerPoint, Outlook) and CRM platforms
 </li>
 <li>
 Ability to travel approximately 30% domestically, with occasional international travel
 </li>
 </ul>
 
 
 
 
 
 What We Offer
 
 
 
 NeurOptics offers a competitive and comprehensive benefits package, including:
 
 <ul>
 <li>
 Competitive compensation (Salary + Bonus)
 </li>
 <li>
 100% employer-paid health benefits for the employee
 </li>
 <li>
 Company-paid vacation, sick time, and holidays
 </li>
 <li>
 Maternity and paternity leave
 </li>
 <li>
 A collaborative, high-performance culture with strong career advancement opportunities
 </li>
 <li>
 Proudly recognized as a
 
 2025 Top Workplace
 
 by the
 
 Orange County Register
 
 </li>
 </ul>
 
 
</div>

Product Manager - Medical Device

Stryker

<div><h3 class="jobSectionHeader">Why join Stryker?</h3>
Looking for a place that values your unique talents? Discover Stryker's award-winning culture. 
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<h3 class="jobSectionHeader">
Job description</h3>
We are excited to be named one of the World&rsquo;s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.<div>
As a Sr. Manager, Marketing you will be responsible for defining and leading the upstream marketing strategy for key portfolios, shaping long-term vision, innovation priorities, and lifecycle management to drive sustainable growth. In this role, you will translate deep customer, clinical, and market insights into differentiated value propositions, portfolio strategy, and new product development direction through close partnership with R&amp;D, Clinical, and cross functional stakeholders. The Sr. Manager, Marketing leads and develops a high-performing team, influences senior leadership decision-making, and ensures strategic alignment from early discovery through commercialization in a dynamic and competitive healthcare environment.
This role requires onsite presence at least 4 days per week, at our Irvine, CA office, to support collaboration, team engagement, and business needs.
What you will do<ul><li>
Lead competitive and market intelligence efforts by advising on major competitors, anticipating future threats, and proactively adjusting strategy to improve market penetration and positioning.</li><li>
Drive deep customer and market understanding through VOC, market research, surveys, and trend analysis, translating qualitative and quantitative insights into clear, actionable business strategies.</li><li>
Identify unmet needs and innovation opportunities by validating key assumptions and partnering cross‑functionally to inform product, service, and portfolio direction.</li><li>
Own portfolio and lifecycle strategy, guiding products from early discovery through launch, growth, pricing optimization, and eventual obsolescence.</li><li>
Lead and influence the new product development process, collaborating with R&amp;D, Clinical, and cross-departmental stakeholders from concept through pre-commercialization planning.</li><li>
Define and communicate long-term portfolio and segment strategies to gain organizational alignment while educating teams on portfolio strategy best practices and benchmarking.</li><li>
Build and sustain strategic KOL relationships, partnering with Clinical Affairs to support evidence generation, clinical claims strategy, and market credibility.</li><li>
Anticipate healthcare market dynamics and environmental trends, proactively recommending adjustments to marketing objectives, brand architecture, and competitive positioning.</li><li>
Guide pricing and value strategies by managing price competition, aligning with business unit goals, and linking marketing investments to customer acquisition and retention objectives.</li><li>
Lead and develop high performing teams, fostering strategic thinking, cross functional collaboration, disciplined forecasting, and effective execution.</li></ul>
What you need
Required<ul><li>
Bachelor&rsquo;s degree</li><li>
10+ years of work experience</li></ul>
Preferred<ul><li>
MBA / Master&rsquo;s Degree</li><li>
7+ years medical device or marketing/sales experience within vascular space</li><li>
4+ years of people management experience</li><li>
Upstream marketing experience in endovascular, vascular, or VTE
</li><li>Demonstrated proficiency in Microsoft Office (Excel, Word &amp; PowerPoint)</li></ul>
$155,900.00 - $259,800.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.</div>
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&amp;D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.</div>

Senior Manager, Marketing (Hybrid)

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