field investigator

Evolution Research Group

<div><p><b>About Company:</b></p><p>
Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I&ndash;IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.</p><p><b>
Why join us?</b> We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.</p><p><b>
Job Description:</b></p><p>
The Clinical Research Coordinator II is responsible for the overall coordination, organization, management, and efficient implementation of clinical trials. The CRC II completes all study related procedures and distributes study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.</p><p><b>
Responsibilities:</b></p><p><b>
General</b></p><ul><li>
Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.</li><li>
Develop draft source documents and review the documents for accuracy and clarity prior to study start up.</li><li>
Develop a mechanism for subject recruitment and ongoing communications with PCP and nursing staff as appropriate.</li><li>
Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.</li><li>
Manage studies with sponsor, and Principal Investigator to ensure compliance with protocol requirements.</li><li>
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.</li><li>
Serve as a mentor and trainer for support staff and new employees once the Clinical Research Coordinator has been approved to do so by the Site Director.</li><li>
Communication of all protocol related issues/problems to the appropriate management staff, including but not limited to questions regarding the conduct of the clinical trial.</li><li>
Contribute to the SOP review and development as delegated by the Site Director.</li></ul><p><b>
Study Management</b></p><ul><li>
Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.</li><li>
Attend the investigator meeting for each assigned protocol, as appropriate.</li><li>
Completion of IRB study renewals and maintain copies of all IRB communications.</li><li>
In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.</li><li>
Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator</li><li>
Review and obtain informed consent from potential study volunteers.</li><li>
Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations.</li><li>
Maintain organized, accurate and complete study records including but not limited to regulatory documents, signed informed consents, IRB correspondence/approvals, source documentation, drug dispensing logs, subject logs and study-related communications.</li><li>
Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.</li><li>
Ensure timely and accurate CRF completion for each study subject.</li><li>
Perform study close-out procedures.</li><li>
Store study records appropriately</li><li>
Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG&rsquo;s objectives.</li></ul><p><b>
Skills and Qualifications:</b></p><ul><li><b>
Education and experience</b><ul><li>
High School Diploma or its equivalent; College degree preferred.</li><li>
Two (2) to four (4) years of experience OR certification as a Clinical Research Coordinator</li><li>
Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.</li><li>
Knowledgeable in medical terminology so as to communicate with physician office and laboratory staff.</li><li>
Demonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.</li><li>
Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.</li></ul></li><li><b>
Requirements</b><ul><li>
Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.</li><li>
Excellent communication skills (interpersonal, written, verbal)</li><li>
Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)</li></ul></li></ul></div>

Clinical Research Coordinator-FT CRC

Information Technology Senior Management Forum

<div><div><p>Posted Date</p>
<p>10/24/2025</p>
</div><div><p>Description</p>
<div>Anti-Money Laundering (AML) Sr. Investigator - Transaction Monitoring Operations (TMO)<p>
The Anti-Money Laundering (AML) Sr. Investigator I supports various AML processes, which might include suspicious activity investigations, currency transaction reporting, global sanctions screening, enhanced due diligence or other AML processes. The AML Sr Investigator I will work closely with AML Process Managers to perform other critical functions.</p><p><b>
Responsibilities</b><b>:</b></p><ul><li>
Build and maintain awareness of the broader context and implications of the various types of risk affecting the business (e.g., financial, legal, reputation, etc.)</li><li>
Review system generated alerts, assess impact to AML processes, conduct research as required, and document results in written format</li><li>
Write suspicious activity reports, files CTR's, address sanctions alerts, and other applicable AML processes in accordance with regulations and time limitations</li><li>
Provide feedback on alert rule effectiveness and partner with management and analysts to design new rules</li><li>
Provide insight into various commercial banking products and services</li><li>
Handle issues as appropriate for advanced investigation and analysis</li><li>
Support team supervisors in executing certain responsibilities</li><li>
Perform special projects as needed</li></ul><p><b>
Basic Qualifications</b><b>:</b></p><ul><li>
High School Diploma, GED or equivalent certification</li><li>
At least 1 year of fraud, investigative or compliance experience</li><li>
At least 1 year of experience with Microsoft Office or Google Suite</li></ul><p><b>
Preferred Qualifications</b><b>:</b></p><ul><li>
Bachelor's Degree in Criminal Justice, Fraud Prevention or Homeland Security</li><li>
2+ years fraud, investigative or compliance experience</li><li>
3+ years of experience in Anti-Money Laundering</li><li>
3+ years of experience in the Financial Services industry</li></ul><p><b>
Are you looking for a challenging role that includes the convenience of working virtually at home? Then a Capital One Anti-Money Laundering Investigator role may be the role for you! You must be within 50 miles driving distance from our Capital One hub in </b><b><i>Wilmington, DE / Richmond, VA / New Orleans, LA / Plano, TX / Jericho, NY / Chicago, IL / McLean, VA / Riverwoods, IL.</i></b></p><p><b>
Work From Home Technology Requirements</b><b>:</b></p><ul><li>
A secure home office environment that is free from background noise and distractions</li><li>
A reliable private internet connection that is not supplied by use cellular data (hot spot)</li><li>
Cable or fiber connections are preferred</li><li>
Internet service download speeds must be at least 5 mbps, with 10+ mbps preferred - check your download speed using a speed test. A sample one can be found here. To test your home internet from your personal computer at home, type www.speedtest.net into the web browser of your personal computer.</li><li>
Sustained ability to maintain latency less than 250 ms in voice calls is required</li><li>
Hard wired connectivity is preferred, any use of wireless connectivity must be Private (non-public) and password protected through WPA2-PSK (AES) encryption. If you have any questions about your encryption, please consult with your internet provider</li><li>
A private network is password protected where you have ownership or line of site to every device on the network</li><li>
Capital One reserves the right to request proof of internet provider, speed and service package from the associate</li><li>
Requirements are subject to change, as new systems and technology is delivered. Capital One reserves the right to modify internet service requirements with sixty (60) days notice.</li></ul><p><b>
Work from Home Living Requirements</b><b>:</b></p><ul><li><b>
Candidates must live within 50 miles driving distance of one of the hub locations based in</b> <i>Wilmington, DE / Richmond, VA / New Orleans, LA / Plano, TX / Jericho, NY / Chicago, IL / McLean, VA / Riverwoods, IL </i>and be comfortable coming in person whenever required with no less than 24 hours notice.</li></ul><p><b><i>
At this time, Capital One will not sponsor a new applicant for employment authorization for this position</i></b><b><i>.</i></b></p><p>
The minimum and maximum full-time annual salaries for this role are listed below, by location. Please note that this salary information is solely for candidates hired to perform work within one of these locations, and refers to the amount Capital One is willing to pay at the time of this posting. Salaries for part-time roles will be prorated based upon the agreed upon number of hours to be regularly worked.</p>
Chicago, IL: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Jericho, NY: $87,400 - $99,700 for AML Sr. Investigator I<br>
<p></p>
McLean, VA: $80,100 - $91,400 for AML Sr. Investigator I<br>
<p></p>
New Orleans, LA: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Plano, TX: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Richmond, VA: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Riverwoods, IL: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Wilmington, DE: $72,800 - $83,100 for AML Sr. Investigator I<p></p><p><br>
Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate&rsquo;s offer letter.</p>
This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). Incentives could be discretionary or non discretionary depending on the plan.<p>
Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the Capital One Careers website. Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level.</p>
This role is expected to accept applications for a minimum of 5 business days.No agencies please. Capital One is an equal opportunity employer (EOE, including disability/vet) committed to non-discrimination in compliance with applicable federal, state, and local laws. Capital One promotes a drug-free workplace. Capital One will consider for employment qualified applicants with a criminal history in a manner consistent with the requirements of applicable laws regarding criminal background inquiries, including, to the extent applicable, Article 23-A of the New York Correction Law; San Francisco, California Police Code Article 49, Sections 4901-4920; New York City&rsquo;s Fair Chance Act; Philadelphia&rsquo;s Fair Criminal Records Screening Act; and other applicable federal, state, and local laws and regulations regarding criminal background inquiries.<p>
If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation, please contact Capital One Recruiting at 1-800-304-9102 or via email at RecruitingAccommodation@capitalone.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations.</p><p>
For technical support or questions about Capital One's recruiting process, please send an email to Careers@capitalone.com</p><p>
Capital One does not provide, endorse nor guarantee and is not liable for third-party products, services, educational tools or other information available through this site.</p><p>
Capital One Financial is made up of several different entities. Please note that any position posted in Canada is for Capital One Canada, any position posted in the United Kingdom is for Capital One Europe and any position posted in the Philippines is for Capital One Philippines Service Corp. (COPSSC).</p>
Anti-Money Laundering (AML) Sr. Investigator - Transaction Monitoring Operations (TMO)<p>
The Anti-Money Laundering (AML) Sr. Investigator I supports various AML processes, which might include suspicious activity investigations, currency transaction reporting, global sanctions screening, enhanced due diligence or other AML processes. The AML Sr Investigator I will work closely with AML Process Managers to perform other critical functions.</p><p><b>
Responsibilities</b><b>:</b></p><ul><li>
Build and maintain awareness of the broader context and implications of the various types of risk affecting the business (e.g., financial, legal, reputation, etc.)</li><li>
Review system generated alerts, assess impact to AML processes, conduct research as required, and document results in written format</li><li>
Write suspicious activity reports, files CTR's, address sanctions alerts, and other applicable AML processes in accordance with regulations and time limitations</li><li>
Provide feedback on alert rule effectiveness and partner with management and analysts to design new rules</li><li>
Provide insight into various commercial banking products and services</li><li>
Handle issues as appropriate for advanced investigation and analysis</li><li>
Support team supervisors in executing certain responsibilities</li><li>
Perform special projects as needed</li></ul><p><b>
Basic Qualifications</b><b>:</b></p><ul><li>
High School Diploma, GED or equivalent certification</li><li>
At least 1 year of fraud, investigative or compliance experience</li><li>
At least 1 year of experience with Microsoft Office or Google Suite</li></ul><p><b>
Preferred Qualifications</b><b>:</b></p><ul><li>
Bachelor's Degree in Criminal Justice, Fraud Prevention or Homeland Security</li><li>
2+ years fraud, investigative or compliance experience</li><li>
3+ years of experience in Anti-Money Laundering</li><li>
3+ years of experience in the Financial Services industry</li></ul><p><b>
Are you looking for a challenging role that includes the convenience of working virtually at home? Then a Capital One Anti-Money Laundering Investigator role may be the role for you! You must be within 50 miles driving distance from our Capital One hub in </b><b><i>Wilmington, DE / Richmond, VA / New Orleans, LA / Plano, TX / Jericho, NY / Chicago, IL / McLean, VA / Riverwoods, IL.</i></b></p><p><b>
Work From Home Technology Requirements</b><b>:</b></p><ul><li>
A secure home office environment that is free from background noise and distractions</li><li>
A reliable private internet connection that is not supplied by use cellular data (hot spot)</li><li>
Cable or fiber connections are preferred</li><li>
Internet service download speeds must be at least 5 mbps, with 10+ mbps preferred - check your download speed using a speed test. A sample one can be found here. To test your home internet from your personal computer at home, type www.speedtest.net into the web browser of your personal computer.</li><li>
Sustained ability to maintain latency less than 250 ms in voice calls is required</li><li>
Hard wired connectivity is preferred, any use of wireless connectivity must be Private (non-public) and password protected through WPA2-PSK (AES) encryption. If you have any questions about your encryption, please consult with your internet provider</li><li>
A private network is password protected where you have ownership or line of site to every device on the network</li><li>
Capital One reserves the right to request proof of internet provider, speed and service package from the associate</li><li>
Requirements are subject to change, as new systems and technology is delivered. Capital One reserves the right to modify internet service requirements with sixty (60) days notice.</li></ul><p><b>
Work from Home Living Requirements</b><b>:</b></p><ul><li><b>
Candidates must live within 50 miles driving distance of one of the hub locations based in</b> <i>Wilmington, DE / Richmond, VA / New Orleans, LA / Plano, TX / Jericho, NY / Chicago, IL / McLean, VA / Riverwoods, IL </i>and be comfortable coming in person whenever required with no less than 24 hours notice.</li></ul><p><b><i>
At this time, Capital One will not sponsor a new applicant for employment authorization for this position</i></b><b><i>.</i></b></p><p>
The minimum and maximum full-time annual salaries for this role are listed below, by location. Please note that this salary information is solely for candidates hired to perform work within one of these locations, and refers to the amount Capital One is willing to pay at the time of this posting. Salaries for part-time roles will be prorated based upon the agreed upon number of hours to be regularly worked.</p>
Chicago, IL: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Jericho, NY: $87,400 - $99,700 for AML Sr. Investigator I<br>
<p></p>
McLean, VA: $80,100 - $91,400 for AML Sr. Investigator I<br>
<p></p>
New Orleans, LA: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Plano, TX: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Richmond, VA: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Riverwoods, IL: $72,800 - $83,100 for AML Sr. Investigator I<br>
<p></p>
Wilmington, DE: $72,800 - $83,100 for AML Sr. Investigator I<p></p><p><br>
Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate&rsquo;s offer letter.</p>
This role is also eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). Incentives could be discretionary or non discretionary depending on the plan.<p>
Capital One offers a comprehensive, competitive, and inclusive set of health, financial and other benefits that support your total well-being. Learn more at the Capital One Careers website. Eligibility varies based on full or part-time status, exempt or non-exempt status, and management level.</p>
This role is expected to accept applications for a minimum of 5 business days.No agencies please. Capital One is an equal opportunity employer (EOE, including disability/vet) committed to non-discrimination in compliance with applicable federal, state, and local laws. Capital One promotes a drug-free workplace. Capital One will consider for employment qualified applicants with a criminal history in a manner consistent with the requirements of applicable laws regarding criminal background inquiries, including, to the extent applicable, Article 23-A of the New York Correction Law; San Francisco, California Police Code Article 49, Sections 4901-4920; New York City&rsquo;s Fair Chance Act; Philadelphia&rsquo;s Fair Criminal Records Screening Act; and other applicable federal, state, and local laws and regulations regarding criminal background inquiries.<p>
If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation, please contact Capital One Recruiting at 1-800-304-9102 or via email at RecruitingAccommodation@capitalone.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodations.</p><p>
For technical support or questions about Capital One's recruiting process, please send an email to Careers@capitalone.com</p><p>
Capital One does not provide, endorse nor guarantee and is not liable for third-party products, services, educational tools or other information available through this site.</p><p>
Capital One Financial is made up of several different entities. Please note that any position posted in Canada is for Capital One Canada, any position posted in the United Kingdom is for Capital One Europe and any position posted in the Philippines is for Capital One Philippines Service Corp. (COPSSC).</p></div>
</div><div><p>Salary</p><p>
72,800.00 - 83,100.00 Annual</p>
</div><div></div><div><div><p>Type</p><div><p>
Full-time</p></div></div></div></div>

Anti-Money Laundering (AML) Sr. Investigator - Transaction Monitoring Operations (TMO)

University Health Partners of Hawaii

<div><p><b>Duties &amp; Responsibilities:</b></p><ul><li>
Independently organizes and manages activities and tasks associated with the conduct of early-phase industry-sponsored and investigator-initiated cancer clinical trials in the Ho&lsquo;&#333;la Early-Phase Clinical Research Center (EPCRC).</li><li>
Works with the clinical trial operation team to identify and inform candidate patients about available clinical protocols, enrolls consenting eligible patients and follows enrolled patients.</li><li>
Collects, documents, and enters data accurately and timely into case report forms, electronic medical record, and electronic data capture systems as required per protocol.</li><li>
Works with the clinical operation staff to ensure standard of care procedures are identified. Responsible for multiple functions needed to access, select and activate protocols and to maintain a high level of training, continuing education, quality control, and regulatory compliance for the enterprise.</li><li>
Works closely with the PI and his/her designee, with nurses and other staff in EPCRC, and with physicians/investigators to foster strong working relationships to ensure compliance with the conduct of industry and investigator-initiated research.</li><li>
Follows the standards and practices of the International Conference on Harmonization for Good Clinical Practices.</li><li>
Handles confidential information responsibly. Maintains confidentiality of patient information in accordance with Health Insurance Portability and Accountability Act (HIPAA).</li><li>
Maintains training as required in human subjects&rsquo; research and all other requirements of UHP.</li><li>
Complies with all legal requirements and company policies.</li><li>
Performs all other duties as assigned.</li></ul><p></p><p><b><br>
QUALIFICATION REQUIREMENTS</b></p><p><b>
Education/Training/Experience</b></p><p>
Minimum:</p><ul><li>
Bachelor&rsquo;s Degree from an accredited four (4) year college or university in a health-related field, or an equivalent number of years of relevant healthcare experience. Relevant education, training, and professional experience in a health-related field may be considered in place of a degree.</li><li>
Ability to interact positively with study participants and others involved with the research environment. Strong written and verbal communication skills. Must possess a valid driver&rsquo;s license (and if use of personal vehicle on the job is required, must also have valid personal driver&rsquo;s insurance equivalent to Hawai&lsquo;i&rsquo;s No-Fault Driver&rsquo;s Insurance) and maintain throughout the duration of employment.</li><li>
Three (3) years of experience working in health research/clinical trials including at least one year of oncology</li></ul><p>
Preferred:</p><ul><li>
Advanced Degree from an accredited college or university in a related field.</li><li>
Previous experience of early-phase industry-sponsored and investigator-initiated cancer clinical trials is preferred.</li></ul><p></p><p><b><br>
Skills Knowledge</b></p><p>
Minimum:</p><ul><li>
Works autonomously with minimal supervision, while also understanding the boundaries of the role, responsibilities, and experience. Seeks guidance and clarification from appropriate protocol-involved personnel when necessary.</li><li>
Demonstrated knowledge in human subjects&rsquo; research and International Conference on Harmonization (ICH)</li><li>
Demonstrated knowledge in Good Clinical Practices (GCP)</li><li>
Demonstrated knowledge in Health Insurance Portability and Accountability Act (HIPAA) requirements .</li><li>
Understanding of research study designs and ethics.</li><li>
Knowledge of and experience with computers and software programs, including word-processing, spreadsheets, and databases.</li><li>
Specialized knowledge of specific cancer care sites conducting clinical trials or of job areas, such as education/training, regulatory, investigational drug accountability/storage, specimen collection/processing, database maintenance/reporting, and regulatory compliance auditing.</li><li>
Demonstrates strong organizational skills, attention to detail, accuracy, desire to learn, and timeliness of work.</li><li>
Strong and effective written and verbal communication skills, and interacts with supervisors, co-workers, and others respectfully and professionally at all times.</li></ul><p></p><p><b><br>
BENEFITS</b></p><ul><li>
Generous time off benefits</li><li>
100% employee health and dental coverage and vision</li><li>
Flexible spending plan</li><li>
Retirement plan with up to 3% dollar-for-dollar company matching contributions</li><li>
100% company paid group Life/AD&amp;D/LTD insurance</li><li>
Employee assistance program (EAP)</li><li>
Pet Insurance, Prepaid legal with competitive rates</li></ul><p></p><p><i><br>
UHP Hawai&lsquo;i is an EEO/AAP employer.</i></p></div>

Clinical Research Coordinator

Sun City Clinical Trials

<p><b>Job Summary:</b></p><p>We are seeking a board-certified Obstetrician-Gynecologist (OBGYN) to provide medical leadership and expertise in clinical trials related to women's health. The physician will be involved in working on studies for new cutting-edge treatments in areas such as reproductive health, pregnancy and childbirth, menopause, gynecologic cancers, hormonal disorders, and other obstetric and gynecologic conditions.</p><p><b>Key Responsibilities:</b></p><ul><li>Provide medical leadership and clinical expertise in the design, implementation, and oversight of clinical trials in obstetrics and gynecology.</li><li>Collaborate with clinical research teams to develop study protocols, informed consent forms, and investigator brochures.</li><li>Monitor clinical trial progress, review safety data, and assess adverse events to safeguard patient welfare.</li><li>Work closely with investigators, clinical sites, and regulatory bodies to ensure protocol adherence and quality data collection.</li><li>Analyze clinical data, contribute to clinical study reports, and assist in manuscript preparation for publication.</li><li>Participate in regulatory submissions, ethics committee meetings, and scientific advisory boards.</li><li>Stay updated on advances in OBGYN clinical research and regulatory requirements.</li><li>Support medical education and business development initiatives related to women&rsquo;s health.</li></ul><p><b>Qualifications:</b></p><ul><li>Medical degree (MD or DO) with board certification in Obstetrics &amp; Gynecology (required)</li><li>Active and valid medical license to practice in Arizona (required)</li><li>Strong analytical skills for interpreting clinical data and safety information</li><li>Excellent communication and collaboration skills</li></ul><p><b>Preferred Skills:</b></p><ul><li>Experience as a Principal Investigator or Sub-Investigator in OBGYN trials.</li><li>Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).</li><li>Knowledge of reproductive endocrinology, maternal-fetal medicine, or gynecologic oncology is a plus.</li><li>Ability to travel occasionally for site visits, investigator meetings, or conferences.</li></ul><p>Job Types: Full-time, Part-time, Contract</p><p>Pay: $100.00 - $250.00 per hour</p><p>License/Certification:</p><ul><li>Medical License (Required)</li></ul><p>Location:</p><ul><li>Chandler, AZ 85224 (Preferred)</li></ul><p>Ability to Commute:</p><ul><li>Chandler, AZ 85224 (Required)</li></ul><p>Ability to Relocate:</p><ul><li>Chandler, AZ 85224: Relocate before starting work (Required)</li></ul><p>Work Location: In person</p><p>Job Types: Full-time, Part-time, Contract</p><p>Pay: $100.00 - $250.00 per hour</p><p>Benefits:</p><ul><li>Dental insurance</li><li>Flexible schedule</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Work Location: In person</p>

Physician for Clinical Research – Obstetrics & Gynecology (OBGYN)

Fidelis Resource Management

<p><b>Key Responsibilities</b></p><ul><li>Review and analyze medical records received from insurance companies.</li><li>Allocate cases to field investigators and monitor field investigation progress.</li><li>Prepare trigger points based on case details to guide investigation.</li><li>Draft clear, accurate investigation reports for submission to clients.</li><li>Handle claim closure communication via email and relevant portals.</li><li>Support team leads and contribute to daily operational workflow.</li></ul><p><b>Required Qualifications</b></p><ul><li>BHMS, BPT, or Post-Graduation in Life Sciences</li></ul><p>(Biology, Biotechnology, Microbiology, Forensic Science, Pharmacy, Bioinformatics, etc.)</p><ul><li>Good command of English (verbal &amp; written)</li><li>Proficiency in MS Office (Word, Excel, Email)</li></ul><p><b>Job Details</b></p><ul><li><b>Location:</b> Wagle Industrial Area, Thane</li><li><b>Working Hours:</b> 9:00 AM &ndash; 7:00 PM</li><li><b>Working Days:</b> 6 Days / Week</li><li><b>Experience:</b> Freshers accepted</li><li><b>Salary (In-Hand):</b> &#8377;16,390 per month (CTC: &#8377;20,000)</li><li><b>Increment:</b> Annual performance-based increment</li></ul><p>Send your resume to: fidelisrmservices@gmail.com<br/>Or call HR directly: <b>9920525398</b></p><p>Job Types: Full-time, Permanent, Fresher</p><p>Pay: &#8377;240,000.00 per year</p><p>Work Location: In person</p>

Medical Claim Analyst/ Executive

PEG, LLC

<p><p>PEG, LLC is in its twenty-seventh year being a diverse energy efficiency, engineering, environmental and management consulting firm operating principally in the Eastern and Central United States.</p><p>As a leader in Home Energy Ratings, a winner of multiple Energy Star Awards, and a standout in the construction industry, PEG has provided Home Energy Ratings for over 250,000 homes. We strive to continually improve building energy efficiency and therefore, the quality of homes and life in the communities that we service.</p><p>PEG LLC offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.</p><p>Please visit our website at to learn more about PEG! </p><p><strong>Competitive Compensation Package with Full Benefits Includes:</strong></p><ul><li>Company-issued Gas Card, Toll Pass, & Vehicle Maintenance Allowance (in addition to salary)</li><li>Company-issued Uniforms, iPhone/iPad, Field Equipment/Tools including Personal Protective Equipment (PPE)</li><li>Flexible Work Schedule Year Round Employment No Weekends Monday to Friday Only!</li><li>Visit a construction site and see the job in action during the interview process!</li><li>Paid On The Job Training Paid Professional Development through Learning/Certification Opportunities</li><li>Pay increases available for approved job-related certifications</li><li>20 Annual Paid Days Off (12 Days of Personal Time Off, Birthday PTO, 7 Company Paid Holidays)</li><li>401(k) Retirement Plan with up to a 4% company match vested immediately</li><li>Company Sponsored Medical Insurance that includes a contribution of up to 50% off the monthly premium</li><li>Dental & Vision Insurance, Short-Term & Long-Term Disability, Accident & Pet Insurance, Basic Life & Supplemental Life Coverage</li></ul><p><strong>THE ROLE</strong></p><p>PEG is searching for a qualified candidate to assist in the inspection and successful implementation of PEGs Risk Management Program.</p><p>In this position, new employees will be provided paid on the job training that will prepare them to maintain systems and procedures to ensure that all structures are built in accordance with the Risk Management Program.</p><p>Excellent communication skills with not only the PEG Team but also PEG clients in a respectful manner is a must. As a representative of PEG, the ideal candidate must be presentable, organized, self-motivated, detail oriented, and dependable.</p><p><strong>Job Location:</strong></p><p>The geographical area assigned to this position includes a 100-mile radius with Richmond, VA at its center.<br><br>Learn more and apply directly by visiting: </p><p><strong>PEG LLC is an Equal Employment Opportunity Employer.</strong></p></p> Required qualifications: <ul><li>Legally authorized to work in the United States</li><li>Reliable transportation to and from work</li><li>Valid driver's license</li><li>Background check</li><li>Willing to travel in state</li></ul><img src="https://www.jobg8.com/Tracking.aspx?v664xeHPeopuP13lIqKCT9mGpK4fWZ6zm" width="0" height="0" />

Risk Management Field Inspector (Richmond, Virginia)

Indian School of Business

<p></p><div><div><div><div><div><div><div><p><b>Location: </b>Hyderabad</p>
<p><b>
No of Positions: </b>1</p>
<p><b>
Reports to Position: </b>Principal Investigator/ Co-Principal Investigator</p>
<p><b>
Reportees to Position: </b>None</p>
<p><b>
Band: </b>FT</p></div></div></div></div></div></div><div></div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>
About the Institute</b></h2>
<p>
MIHM is an interdisciplinary research centre at ISB that provides insights on healthcare delivery and management to policymakers, public institutions, and corporates to enable the creation of better health systems through integrated elements of research, education and outreach.</p></div></div></div></div></div></div><div></div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>
Job Purpose</b></h2>
<p>
To support research on vaccine cold chain innovation by contributing to data-driven analysis, field research, and modelling to improve last-mile vaccination delivery and assess climate-health linkages.</p></div></div></div></div></div></div><div></div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>
Job Outline</b></h2>
<p>
This role provides an opportunity to work on a high-impact research project examining an Indian-origin healthcare innovation that enhances vaccine delivery in challenging geographies. The position involves supporting analytical, field, and policy-relevant research at the intersection of healthcare, climate, and supply chain optimization. The Research Analyst will work closely with ISB faculty and partners to contribute to research design, data analysis, and dissemination of insights.</p></div></div></div></div></div></div><div></div><div><div><div><div><div><div><h2 class="jobSectionHeader"><b>
Job Specifications</b></h2>
<h4 class="jobSectionHeader"><b>Knowledge / Education:</b></h4>
<ul><li>Master&rsquo;s degree in Operations Research, Industrial Engineering, Statistics or Economics.</li>
<li>Exceptional candidates with an undergraduate degree and strong analytical training or relevant work experience may also be considered.</li>
</ul><h4 class="jobSectionHeader"><b>Specific Skills:</b></h4>
<ul><li>Strong motivation to work at the intersection of healthcare, climate, and supply chain research.</li>
<li>Ability to independently drive parts of the research process such as data analysis, model development, and stakeholder coordination.</li>
<li>Good understanding of mathematical modelling, disease modelling, econometric analysis, supply chain analysis, and experimental design.</li>
<li>Excellent written and verbal communication skills, problem-solving ability, and work ethic.</li>
</ul><h4 class="jobSectionHeader"><b>Mandatory Experience:</b></h4>
<ul><li>Minimum 1 year of professional experience in research, consulting, or related analytical work (including internships or research assistantships).</li>
<li>Prior exposure to health systems, climate research, or supply chain analysis preferred.</li>
</ul><h3 class="jobSectionHeader"><b>Key Responsibilities</b></h3>
<ul><li>Conduct research on vaccine cold chain innovation focusing on supply chain optimization, climate, and sustainability aspects.</li>
<li>Support multiple stages of research including literature review, data gathering, cleaning, exploratory analysis, quality checks, and report preparation.</li>
<li>Develop mathematical and econometric models for supply chain and disease modelling.</li>
<li>Design and conduct surveys, interviews, and field studies to collect performance data.</li>
<li>Liaise with stakeholders such as development agencies and health ministries to access contextual data and insights.</li>
Contribute to dissemination of findings through reports, presentations, and research papers.<br>
<li>
</li>
</ul><div><div><div><div><b>Job Interface / Relationships</b></div>
</div><br>
<div><div><b>Internal</b></div>
<div>
<p><b>External</b></p></div></div><br>
<div>
<div><ul><li>MIHM research team, ISB faculty, and project staff</li>
<li>Other departments including Grants, Finance, Legal, and IT</li>
</ul>
</div><div><ul><li>Grantor research/programme team</li>
<li>Vendors &amp; Consultants</li>
<li>Sub-grantees/data collection agencies</li>
<li>IRB Boards, governments, other stakeholders</li></ul></div><br>
</div><br>
</div></div><p></p><h3 class="jobSectionHeader"><b>How to Apply?</b></h3>
<p>
Send an email to maxinstitute@isb.edu with the subject line &ldquo;Application for Research Analyst &ndash; Vaccine Cold Chain Innovation Project&rdquo; along with a copy of your CV. Applications will be reviewed until the position is filled. Only shortlisted candidates will be contacted for an interview.</p></div></div></div></div></div></div><div></div><div><div><div><div><div><div><div><div>
Hyderabad Campus</div><div><p>
Indian School of Business</p>
<p>
Gachibowli, Hyderabad - 500111</p></div></div><p></p><div><div><br>
Timings : Monday- Friday, 08:00 AM IST to 06:00 PM IST</div><ul><li><p>
040 23187777</p></li><li><p>
0172 4591800</p></li><li><p>
careers_hyderabad@isb.edu</p></li><li><p>
careers_mohali@isb.edu</p></li><li><p>
careers_ra@isb.edu</p></li></ul></div></div><div><div><div>
Mohali Campus</div><div><p>
Indian School of Business</p>
<p>
Knowledge City</p>
<p>
Sector 81, SAS Nagar ,Mohali - 140 306</p></div></div></div></div></div></div></div></div></div><div></div>

Research Analyst at ISB MIHM - Hyderabad

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