We have other current jobs related to this field that you can find below

  • Contracts Analyst

    2 months ago


    Irvine, United States Careerbuilder-US Full time

    Job Title: Contracts Analyst / Contracts Specialist Job Location: Irvine, CA Zip Code: 92614 Top 3/5 Skills: Contracts Analysis/Agreement Analysis Job Description Must have: Contracts analysis experience SUMMARY: · The main function of a clinical contracts analyst is to initiate, draft, redline, and negotiate 3rd party...


  • Irvine, United States Cypress HCM Full time

    Job DescriptionJob DescriptionClinical Operations Associate AnalystWe have an exciting opportunity for a Clinical Operations Associate Analyst position with one of the top medical device companies in the country. Responsibilities:Identify, develop, recommend, and implement, moderately complex process development and process improvement solutions to optimize...


  • Irvine, United States DIALITY INC Full time

    Job DescriptionJob DescriptionJob TitleClinical SpecialistDepartmentClinical AffairsHiring Manager TitleAssociate Director, Clinical AffairsPosition TypeExempt Company & Job Overview:Diality Inc, a privately held medical device company located in Irvine, CA is committed to improving the quality of life for patients with kidney disease. We are developing a...


  • Irvine, United States DIALITY INC Full time

    Job DescriptionJob DescriptionJob TitleClinical SpecialistDepartmentClinical AffairsHiring Manager TitleAssociate Director, Clinical AffairsPosition TypeExempt Company & Job Overview:Diality Inc, a privately held medical device company located in Irvine, CA is committed to improving the quality of life for patients with kidney disease. We are developing a...


  • Irvine, California, United States Cynet Systems Full time

    Job OverviewWe are seeking a Clinical Research Associate to support our client in their clinical research initiatives.Position Title: Clinical Research AssociateLocation: RemoteEmployment Type: ContractCompensation: $38.56/hr - $43.56/hrKey Responsibilities:Assist in the evaluation and upkeep of study and site documentation, aiding in the management of...

  • Contract Analyst

    2 weeks ago


    Irvine, United States The Intersect Group Full time

    Contract Analyst for Vendor Management TeamAt least 6 months-could possibly convertvendor renewals, legal terminology, insurance policiesreviewing existing vendor contracts in renewal stageHeavy redliningComparing new legal terms-update terms as necessaryParalegal or contract backgroundContracts for tech, phone systems, HP, vendorsAt least 3 years of...

  • Contract Analyst

    2 weeks ago


    Irvine, United States The Intersect Group Full time

    Contract Analyst for Vendor Management TeamAt least 6 months-could possibly convertvendor renewals, legal terminology, insurance policiesreviewing existing vendor contracts in renewal stageHeavy redliningComparing new legal terms-update terms as necessaryParalegal or contract backgroundContracts for tech, phone systems, HP, vendorsAt least 3 years of...


  • Irvine, United States KellyConnect | Contact Center Solutions Full time

    Feeling stuck? Put your career in motion with a great, new opportunity. Join the Kelly team as a Senior Contract Analyst to work at JJ Vision, a premier medical device company in Irvine, CA. Were here every step of the way to help you and your career be the best it can be. Bring your energy and expertise. Well help you get where you want to be. Salary/Pay...


  • Irvine, United States Ledgent Technology Full time

    Contract: 1 Year Pay: Up to $36.67 per hour, W2Location: Irvine, CASummary:Analyze and process payments associated with clinical trials, ensure alignment with contractual and trial requirements and manage the lifecycle of the payment.Job Responsibilities:* Process complex payments (e.g, invoices, expenses) clinical and/or medical affairs contractual costs...


  • Irvine, United States Ledgent Technology Full time

    Contract: 1 Year Pay: Up to $36.67 per hour, W2Location: Irvine, CASummary:Analyze and process payments associated with clinical trials, ensure alignment with contractual and trial requirements and manage the lifecycle of the payment.Job Responsibilities:* Process complex payments (e.g, invoices, expenses) clinical and/or medical affairs contractual costs...


  • Irvine, United States KellyConnect | Contact Center Solutions Full time

    Feeling stuck? Put your career in motion with a great, new opportunity. Join the Kelly® team as a Senior Contract Analyst to work at JJ Vision, a premier medical device company in Irvine, CA. We’re here every step of the way to help you and your career be the best it can be. Bring your energy and expertise. We’ll help you get where you want to...


  • Irvine, United States KellyConnect | Contact Center Solutions Full time

    Feeling stuck? Put your career in motion with a great, new opportunity. Join the Kelly® team as a Senior Contract Analyst to work at JJ Vision, a premier medical device company in Irvine, CA. We’re here every step of the way to help you and your career be the best it can be. Bring your energy and expertise. We’ll help you get where you want to...


  • Irvine, California, United States Actalent Full time

    Position Title: Senior Clinical Research ManagerWe are in search of a Senior Clinical Research Manager to lead the strategic operational oversight of both pre-market and post-market clinical trials.This position emphasizes the improvement of effective execution in review and approval workflows, contract negotiations, and communication with clinical study...


  • Irvine, United States Johnson & Johnson Full time

    Description Mentor Corporation, a member of the Johnson & Johnson Family of Companies, is currently recruiting a Sr. Clinical Research Specialist located in Irvine, CA.*There is already an identified candidate for the role.At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex...


  • Irvine, California, United States Johnson & Johnson Full time

    Mentor Corporation, a member of the Johnson & Johnson Family of Companies, is currently recruiting a Sr. Clinical Research Specialist located in Irvine, CA.*There is already an identified candidate for the role.At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are...


  • Irvine, United States Marquee Staffing - Healthcare Full time $47 - $50

    Job DescriptionJob DescriptionOur global medical device manufacturer is hiring a RN to assist with the clinical trials of our Class 1 Medical Devices in the Irvine, CA area! Work Schedule: Mon-Fri 8am-4:30pmDuties & Responsibilities:- Assist with/conduct broad range of clinical trial duties, including equipment setup, collect data, verify results,...


  • Irvine, United States Kelly Science, Engineering, Technology & Telecom Full time

    Clinical Finance Coordinator, CSSEssential Functions & Duties,Provides financial support for multiple client departments in accordance with Good Clinical Practice (GCP), guidelines, standards, federal regulations, and SOPs.Strong support of a variety of finance duties including but not limited to payment reconciliation, accruals, Purchase Orders, and other...


  • Irvine, United States Kelly Science, Engineering, Technology & Telecom Full time

    Clinical Finance Coordinator, CSSEssential Functions & Duties,Provides financial support for multiple client departments in accordance with Good Clinical Practice (GCP), guidelines, standards, federal regulations, and SOPs.Strong support of a variety of finance duties including but not limited to payment reconciliation, accruals, Purchase Orders, and other...


  • Irvine, United States Ledgent Technology Full time

    Medical Device client is seeking a Clinical Research Coordinator/Study Manager in Irvine, CA!Assoc Spec, Clinical ResearchDuration - 1 YearLocation - Irvine, CAMax Pay - $45.05 Summary: The main function of the Associate Clinical Research Specialist, is to perform study start-up and conduct activities, ensuring clinical studies are conducted and reported in...


  • Irvine, United States Ledgent Technology Full time

    Medical Device client is seeking a Clinical Research Coordinator/Study Manager in Irvine, CA!Assoc Spec, Clinical ResearchDuration - 1 YearLocation - Irvine, CAMax Pay - $45.05 Summary: The main function of the Associate Clinical Research Specialist, is to perform study start-up and conduct activities, ensuring clinical studies are conducted and reported in...

Clinical Contracts Analyst, Trials and Sites

2 months ago


Irvine, United States Edwards Lifesciences Gruppe Full time

We have made changes to enhance your experience. If you have applied for a job previously, you will need to create a new account. Thank you for your patience.

Clinical Contracts Analyst, Trials and Sites page is loaded

Clinical Contracts Analyst, Trials and Sites

Apply

locations

USA - California – Irvine

time type

Full time

posted on

Posted 27 Days Ago

job requisition id

Req-33921

Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes. Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. As

the Clinical Contracts Analyst , you will negotiate and develop contracts and budgets associated with clinical trials, ensure contracts comply with regulations and manage the lifecycle of contracts.

The position will be on-site at our Irvine headquarters 5 days/week.

How you will make an impact: Specific to clinical trial sites, prepare initial contract(s) and draft(s); redline and negotiate contracts, utilizing Legal Department templates; demonstrate clinical knowledge and adhere to regulatory requirements; assist in proposing new language for templates. Negotiate site-specific clinical trial budgets for per-patient procedures and trial-related costs based on basic financial knowledge and in adherence with regulatory requirements. Identify risks and analyze potential impact to company; communicate risk to key stakeholders. Communicate and collaborate with key internal stakeholders, including THV Project Managers, Legal, Compliance and Finance to obtain or clarify data required for budgets and contracts; share contracting strategies and discuss potential risks to trial timelines and deliverables. Collaborate with external stakeholders (hospital and/or university research office, finance office, and external or internal counsel) to negotiate budgets and contracts and to collect required documentation for executed contracts. Submit proposed final draft and supporting documentation through Legal Department’s electronic contracts management system for contract approval and secure appropriate signatures within specified signing authority; utilize company systems to store executed contracts and manage on-going assignments. What you will need (required)

: Bachelor's Degree in related field Minimum 3 years of previous related experience in contract preparation,

negotiation, redlining, and budget negotiations Experience in healthcare related contracts What else we look for (preferred)

: Previous clinical research/clinical trial experience Strong budget negotiation experience Contract or paralegal certification Additional Skills: Proven expertise in Microsoft Office Suite, including PowerPoint, Excel, and Word and ability to operate general office machinery Good written and verbal communication skills and interpersonal relationship skills Demonstrated problem-solving and critical thinking skills Moderate knowledge and understanding of Edwards policies, procedures and guidelines relevant to contract negotiation and administration Moderate knowledge of medical terminology and healthcare compliance and privacy regulations (e.g. HIPAA and Sunshine Act) Moderate understanding of regulatory requirements (e.g., CFR, GCP) and documents Advanced proficiency in Microsoft Office Suite, including Excel, and Word Ability to manage confidential information with discretion Strict attention to detail Ability to interact professionally with all organizational levels Ability to manage competing priorities in a fast paced environment Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific project Ability to build productive internal/external working relationships For California, the base pay range for this position is $65,000 to $92,000 (highly experienced). The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience).Applications will be accepted while this position is posted on our Careers website. E dwards is an Equal

Opportunity/Affirmative

Action employer including protected Veterans and individuals with disabilities. COVID Vaccination Requirement Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

#J-18808-Ljbffr