
Unknown Employer · Sweden
Description The Associate II, Payment Services (Deposits) processes a high volume of daily banking transactions in a timely and complete manner through a variet...
Description The Associate II, Payment Services (Deposits) processes a high volume of daily banking transactions in a timely and
complete manner through a variety of complex technology systems. This position also proactively conducts quality control measures
(QC) on assigned processes. The Associate II consistently evaluates transactions for critical risk including approval/limit
requirements and fraud, reporting internally or contacting the member as appropriate. Here’s what you can expect from the job and
what you need to be successful: What You'll Do: Process a high volume of daily transactions including wire transfers (Domestic,
Foreign, Exceptions, Outgoing), Automatic Clearing House (ACH) originations, mobile deposits, mailed in payments, lockbox payments
and Person to Person (P2P) transfers Navigate a variety of complex technology systems with various processing functions and
deadlines, meeting department Service Level Agreements (SLAs). These systems include core processors for deposit accounts (Fiserv
DNA), GFX for wire transfers (Finastra), Ensenta (Jack Henry) for mobile banking and ATM transactions, Alkami for online banking,
Fed Advantage for ACH processing, PNC for foreign currency and checks, and Single Point (US Bank) for lockbox research Proactively
review and research transactions for potential fraud; prepare full report on suspicious transactions and send to Fraud Liaison for
further review Conduct research and validation as required in processing mailed in payments, lockbox payments, online banking
transactions and Bill Pay transactions Communicate with members and internal partners as appropriate to achieve positive and
responsive customer service Respond to inquiries from internal associates assisting members regarding payment/deposits Assess
member financial resources using the core system to complete transactions Adhere to appropriate levels of approval and limit
requirement in evaluating transactions Research and resolve member, vendor and internal issues by adjusting processes as
appropriate Perform testing for periodic system upgrades and enhancements Actively provides feedback around process improvements
to support effectiveness in operational functions, procedures and work methods Assists with projects as a Subject Matter Expert
for testing, business requirements, process mapping Essential Skills: Minimum one year’s experience in the financial industry,
ideally in payment operations or back-office operation Experience handling sensitive information in a confidential manner
Experience in reviewing and identifying suspicious/fraudulent activity is preferred Strong analytical and problem-solving skills;
ability to resolve complex issues with minimal direction Ability to effectively prioritize tasks, handling a variety of
responsibilities simultaneously Proficiency with current version Microsoft Office Suite products (Word, Excel, PowerPoint and
Outlook) Certification/License: N/A Minimum Education: High School Diploma with some post-secondary education preferred Location:
Hillsboro Corporate Office – Hillsboro, OR 97124 (HYBRID) Target Compensation in Hillsboro, OR: $22.33 to $26.68 per hour + annual
bonus Who We Are: What makes First Tech different? Click here to learn more! Every great journey begins with a bold idea—and ours
is no different. First Tech and DCU were founded on the belief that financial solutions should put people first. That belief has
fueled decades of innovation and service, rooted in the tech sector and expanding to support members from all walks of life.
Employees are eligible for: Traditional medical, dental, and vision coverage Generous 401(k) match Paid Time Off: - You’ll accrue
up to 15 days in your first year. In addition, you’ll receive 40 hours of sick time and 3 personal days, which refresh annually
Paid federal holidays Special employee pricing on lending products such as mortgage, auto, and personal loans (eligibility subject
to standard account requirements and underwriting criteria Employment Statements: First Tech is an equal opportunity employer, and
we value diversity, inclusion, and equity at our company. We evaluate qualified applicants without regard to race, color,
religion, age, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected
characteristics. If you’re applying for a job and need a reasonable accommodation for any part of the employment process, please
send an email to [email protected] and let us know the nature of your request and contact information. Please note that only those
inquiries concerning a request for reasonable accommodation will be responded to from this email address First Tech is not
currently offering Visa transfer or sponsorship for this position
Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. Essential functions of the job include but are not limited to: * Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner * May perform data entry for paper-CRF studies, as needed * May perform quality control of data entry * May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders * May assist in building clinical databases * Conduct database build UAT and maintain quality controlled database build documentation * Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. * Responsible for creating, revising, appropriate versioning and maintaining data management documentation. * Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed * Review and query clinical trial data according to the Data Management Plan * Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM * Run patient and study level status and metric reporting * Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency * Assist with coordinating SAE/AE reconciliation * Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables * May assist with SAS programming and quality control of SAS programs used in the Data Management department * May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders * May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project * May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities * Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues * May present software demonstrations/trainings, department/company training sessions, present at project meetings * May require some travel * Perform other duties as assigned Job Qualifications: * Bachelors and/or a combination of related experience * Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. * Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook * Able to handle a variety of clinical research tasks * Excellent organizational and communication skills * Professional use of the English language; both written and oral Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. Please, apply in English. #LI-EK1 #LI-Remote ---------------------------------------------------------------------------------------------------------------------------------- Any data provided as a part of this application will be stored in accordance with our Privacy Policy. [https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&reserved=0] For CA applicants, please also refer to our CA Privacy Notice [https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&reserved=0]. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com [myHR@precisionmedicinegrp.com]. Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com [myHR@precisionmedicinegrp.com] so we can investigate and take appropriate action.
Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. Essential functions of the job include but are not limited to: * Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner * May perform data entry for paper-CRF studies, as needed * May perform quality control of data entry * May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders * May assist in building clinical databases * Conduct database build UAT and maintain quality controlled database build documentation * Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. * Responsible for creating, revising, appropriate versioning and maintaining data management documentation. * Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed * Review and query clinical trial data according to the Data Management Plan * Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM * Run patient and study level status and metric reporting * Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency * Assist with coordinating SAE/AE reconciliation * Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables * May assist with SAS programming and quality control of SAS programs used in the Data Management department * May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders * May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project * May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities * Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues * May present software demonstrations/trainings, department/company training sessions, present at project meetings * May require some travel * Perform other duties as assigned Job Qualifications: * Bachelors and/or a combination of related experience * Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. * Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook * Able to handle a variety of clinical research tasks * Excellent organizational and communication skills * Professional use of the English language; both written and oral Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. Please, apply in English. #LI-EK1 #LI-Remote ---------------------------------------------------------------------------------------------------------------------------------- Any data provided as a part of this application will be stored in accordance with our Privacy Policy. [https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&reserved=0] For CA applicants, please also refer to our CA Privacy Notice [https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&reserved=0]. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com [myHR@precisionmedicinegrp.com]. Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com [myHR@precisionmedicinegrp.com] so we can investigate and take appropriate action.
Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. Essential functions of the job include but are not limited to: * Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner * May perform data entry for paper-CRF studies, as needed * May perform quality control of data entry * May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders * May assist in building clinical databases * Conduct database build UAT and maintain quality controlled database build documentation * Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. * Responsible for creating, revising, appropriate versioning and maintaining data management documentation. * Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed * Review and query clinical trial data according to the Data Management Plan * Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM * Run patient and study level status and metric reporting * Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency * Assist with coordinating SAE/AE reconciliation * Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables * May assist with SAS programming and quality control of SAS programs used in the Data Management department * May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders * May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project * May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities * Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues * May present software demonstrations/trainings, department/company training sessions, present at project meetings * May require some travel * Perform other duties as assigned Job Qualifications: * Bachelors and/or a combination of related experience * Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. * Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook * Able to handle a variety of clinical research tasks * Excellent organizational and communication skills * Professional use of the English language; both written and oral Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. Please, apply in English. #LI-EK1 #LI-Remote ---------------------------------------------------------------------------------------------------------------------------------- Any data provided as a part of this application will be stored in accordance with our Privacy Policy. [https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fprivacy-policy%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=9DgboiHTFPrNYVhdKhyfdwVyNYwUvZbP%2FroLdWIIfxw%3D&reserved=0] For CA applicants, please also refer to our CA Privacy Notice [https://nam12.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.precisionmedicinegrp.com%2Fca-applicants-privacy-notice%2F&data=05%7C01%7Czeta.larcon%40precisionmedicinegrp.com%7Cb58fe8b0c3ea4dd2e79d08db5bd09a25%7Cb71ff3f628164ca8a9b938f820f91ad1%7C0%7C0%7C638204723732367131%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C3000%7C%7C%7C&sdata=tfAqqMZsG%2B11IchL45HFFVbfECCkYqQpNr0PQxrMFJU%3D&reserved=0]. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com [myHR@precisionmedicinegrp.com]. Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at myHR@precisionmedicinegrp.com [myHR@precisionmedicinegrp.com] so we can investigate and take appropriate action.