clinical researcher

DataAnnotation

<div>
 We are looking for a Clinical Researcher to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.
 <br/>
 <br/>
 In this role you will need to hold an expert level of biology. Other related fields include, but are not limited to: Biology and/or Biochemistry.
 <br/>
 <br/>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This is a full-time or part-time REMOTE position
  </li>
  <li>
   You&rsquo;ll be able to choose which projects you want to work on
  </li>
  <li>
   You can work on your own schedule
  </li>
  <li>
   Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Give AI chatbots complex biology questions and evaluate their outputs
  </li>
  <li>
   Evaluate the quality produced by AI models for correctness and performance
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Fluency in English (native or bilingual level)
  </li>
  <li>
   Detail-oriented
  </li>
  <li>
   Understanding of cell biology, genetics, biochemistry, and experimental methods
  </li>
  <li>
   A current, in progress, or completed Master's and/or PhD is preferred but not required
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Notes
  <br/>
  <br/>
 </strong>
 Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Only applicants in the United States will be considered for this role. This is an independent contract position.
 <br/>
 <br/>
 #bio
</div>


Clinical Researcher

MD Anderson Cancer Center

<div><b>Position Title: Instructor, Clinical Faculty Appointment</b><br>
<br>
<b>D</b><b>e</b><b>p</b><b>ar</b><b>t</b><b>me</b><b>n</b><b>t:</b><b>Lymphoma/Myeloma</b><br>
<br>
<b>D</b><b>i</b><b>v</b><b>i</b><b>s</b><b>i</b><b>o</b><b>n</b><b>:</b><b>C</b><b>a</b><b>n</b><b>cer </b><b>M</b><b>e</b><b>d</b><b>i</b><b>c</b><b>i</b><b>n</b><b>e</b><br>
<br>
<b>R</b><b>e</b><b>p</b><b>orts</b><b>t</b><b>o</b><b>:</b><b>Department Chair</b><br>
<br>
The following C.A.R.E effort complies with all policies and procedures.<div></div><div><div><div><br>
<b>
Activity</b><br>
</div><div><br>
<b>Reported Actual Percent of Effort</b></div></div><div></div><div><div><br>
Clinical Care<br>
</div><div><br>
20%</div></div><div></div><div><div><br>
Administrative Activities<br>
</div><div><br>
2%</div></div><div></div><div><div><br>
Research Activities<br>
</div><div><br>
75%</div></div><div></div><div><div><br>
Educational Activities<br>
</div><div><br>
3%</div></div><div></div><div><div><br>
Extramural Service (described in text)</div></div></div><br>
<div></div>
<b>
M</b><b>I</b><b>SS</b><b>IO</b><b>N </b><b>S</b><b>T</b><b>A</b><b>TE</b><b>M</b><b>E</b><b>N</b><b>T</b><br>
<br>
The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and prevention, and through education for undergraduate and graduate students, trainees, professionals, employees and the public.<br>
<br>
<b>S</b><b>U</b><b>M</b><b>M</b><b>ARY</b><br>
<br>
The primary function of the Instructor position is to be an active member and leader of the clinical and research team and to apply technical expertise and experience to plan, coordinate, design, assist, and supervise the implementation of clinical and research projects, the evaluation and interpretation of research data, and the quality of resulting publications.<br>
<br>
<ul><li>Scope: Perform clinical and research activities in a mentored leadership role of an active clinical and research team for immunotherapies and vaccines, with the goal of developing into an independent clinical investigator.</li></ul><br>
<ul><li>The ideal candidate will meet the following criteria:</li></ul><br>
o Prior expertise and knowledge in clinical research protocols, processing of human and mouse blood and tissue samples, molecular biology, biochemistry, cell biology, immunology, flow cytometry, and tissue culture.<br>
<br>
o Strong and the comprehensive background in cancer research.<br>
<br>
o Commitment to write and submit competitive grant applications as principal investigator or co-investigator under the oversight of a research mentor.<br>
<br>
o Aspiration and resourcefulness to achieve greater scientific independence through the development of collaborative research projects.<br>
<br>
o Participate in the training of clinical and research, postdoctoral fellows, clinical fellows, graduate, medical and college students, as well as laboratory technicians.<br>
<br>
o A collaborative and friendly member/leader of a large cancer research group including research scientists, clinicians, statisticians, trainees, and supportive staff.<br>
<br>
<b>C</b><b>OR</b><b>E </b><b>V</b><b>ALUE</b><b>S</b><br>
<br>
<b>C</b><b>ar</b><b>i</b><b>ng</b><b>B</b><b>eha</b><b>v</b><b>i</b><b>o</b><b>rs</b><br>
<br>
<ul><li>Courtesy: Is respectful and courteous to each other at all times</li></ul><br>
<ul><li>Friendliness/Teamwork: Promotes and rewards teamwork and inclusiveness; Is sensitive to the concerns of our patients and our co-workers</li></ul><br>
<b>
I</b><b>n</b><b>t</b><b>e</b><b>g</b><b>r</b><b>it</b><b>y</b><b>B</b><b>eha</b><b>v</b><b>i</b><b>ors</b><br>
<ul><li>
Reliability: Communicates frequently, honestly and openly</li><li>
Accountability: Holds self and others accountable for practicing our values</li><li>
Safety: Notices a safety concern and brings it to someone's attention; Models safe behaviors (wears badge, washes hands, keeps work area clean and orderly)</li></ul><br>
<b>
D</b><b>i</b><b>sco</b><b>v</b><b>ery</b><b>B</b><b>eha</b><b>v</b><b>i</b><b>o</b><b>r</b><b>s</b><br>
<ul><li>
Responsiveness: By his/her actions, creates an environment of trust; Encourages learning, creativity and new ideas</li><li>
Personal Leadership/Self-Initiative: Helps others to identify and solve problems; Seeks personal growth and enables others to do so</li></ul><br>
<b>
Safety Behaviors</b><br>
<ul><li>
Create a sense of security and empowerment and are committed to keeping one another free from harm.</li><li>
Embrace a framework and best practices for the highest quality of care and service.</li>
Inspire trust by modeling excellence in our work and acceptance of each person's contributions.<br>
<li>
</li></ul><br>
<br>
<b>Stewardship Behaviors</b><br>
<ul><li>
Prioritize the health and well-being of each other.</li><li>
Act responsibly to safeguard the institution's finances.</li><li>
Ensure the proper care and use of time, data, materials, equipment and property afforded to us.</li></ul><br>
<b>
K</b><b>E</b><b>Y</b><b>F</b><b>UNCTIONS</b><br>
<br>
1. Participate in patient care services in the outpatient setting and/or inpatient service to further develop clinical skills in the areas of lymphoma and/or myeloma.<br>
<br>
2. Impact the quality and advancement of cancer research efforts within the Department and MD Anderson Cancer Center with a primary focus on Lymphoma / Myeloma.<br>
<br>
3. Plan, organize, direct, assist, and participate in experiments and assays related to clinical patient research samples, animal models and in vitro studies in a research laboratory.<br>
<br>
4. Develop novel independent research projects.<br>
<br>
5. Develop and maintain standard procedures and clinical protocols to ensure the quality and integrity of procedures performed and the overall operation of the laboratory.<br>
<br>
6. Exercise considerable initiative in planning and executing the details of experiments and in evaluating and interpreting the results. Responsible for the participation and involvement of other laboratory members and collaborators in the development of laboratory techniques and research projects. Provide expertise, knowledge, or techniques to troubleshoot problems.<br>
<br>
7. Participate in laboratory meetings to present research findings to colleagues. Potential to attend academic conferences or meetings for oral or visual production of posters.<br>
<br>
8. Participate in the guidance, teaching, supervision, and assistance of trainees, collaborators, and laboratory members to accomplish research or other laboratory duties as required.<br>
<br>
9. Produces manuscripts, research proposals and grant funding, and collaborates with laboratory members to reinforce expertise and advance research objectives including the publication of articles and presentations at scientific meetings.<br>
<br>
10. All conducted projects require review literature, experimental design, alternative approaches, organization, timeline, coordination, data interpretation, future directions and monthly progress report to immediate supervisor.<br>
<br>
11. Comply with all policies and procedures.<br>
<br>
12. Other duties as assigned.<br>
<br>
<b>C</b><b>OR</b><b>E </b><b>C</b><b>O</b><b>M</b><b>PETE</b><b>NCI</b><b>ES</b><br>
<br>
<ul><li>IC - Analytical Thinking:</li></ul><br>
o Gather relevant information systematically;<br>
<br>
o Break down problems into simple components; and<br>
<br>
o Make sound decisions.<br>
<br>
<ul><li>IC - Build Relationships:</li></ul><br>
o Initiate, develop, and manage relationships and networks; and<br>
<br>
o Show sincere interest in others and their concerns.<br>
<br>
<ul><li>IC - Innovative Thinking:</li></ul><br>
o Approach problems with curiosity and open-mindedness; and<br>
<br>
o Offer new ideas, solutions and/or options.<br>
<br>
<ul><li>IC-Team with Others:</li></ul><br>
o Encourage collaboration and input from all team members; value the contributions of all team members;<br>
<br>
o Balance individual and team goals.<br>
<br>
<ul><li>IC-Equipment Usage &amp; Safety Preparedness:</li></ul><br>
o Employee maintains expectations for safety preparedness<br>
<br>
o Including but not limited to: Orientation to new equipment, Employee Education Event, CPR training, fire drills<br>
<br>
The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition.<br>
<br>
This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment.<br>
<br>
It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state, or local laws unless such distinction is required by law.http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html<br>
<br>
Additional Information
<br>
<ul><li>Requisition ID: 179178
</li><li>Employee Status: Regular
</li><li>Minimum Salary: US Dollar (USD) 0
</li><li>Midpoint Salary: US Dollar (USD) 0
</li><li>Maximum Salary : US Dollar (USD) 0
</li><li>FLSA: exempt and not eligible for overtime pay
</li><li>Work Location: Onsite
</li></ul><br>
#LI-Onsite</div>

Instructor, Clinical Faculty Appointment (CFA) - Lymphoma-Myeloma

LifeScanners

<p><b>Job Title</b>: Oral Pathologist</p><p><b>Company</b>: DIGIPATH AI: LifeScanners HealthCare Pvt Ltd</p><p><b>Location</b>: Chennai, India</p><p><b>Experience</b>: MDS in Oral and Maxillofacial Pathology (1-2years of experience/ Freshers, provided they pass our training regimen)</p><p><b>Role Overview</b></p><p>The Oral Pathologist at DIGIPATH AI will play a key role in diagnostic interpretation, clinical research, and digital pathology innovation. The position combines core oral pathology expertise with opportunities to contribute to AI-driven diagnostic tools such as VELscan and DNA Ploidy systems. The role emphasizes a balance of diagnostic reporting, research, education, and community engagement.</p><p><b>Role and Responsibilities:</b></p><p><b>1. Diagnostic Reporting &amp; Quality Compliance</b></p><ul><li>Accurately review and report LBC PAP smears and DNA Ploidy test samples as per company protocols.</li><li>Answer case-specific questions raised by clinicians and ensure clarity of diagnostic insights.</li><li>Internally audit lab protocols to ensure adherence to NABL standards and SOPs.</li><li>Identify and implement improvements in lab practices to maintain diagnostic excellence.</li></ul><p><b>2. Research and Development</b></p><ul><li>Interpret, summarize, and simplify complex scientific literature related to VELscan and DNA Ploidy.</li><li>Lead or collaborate on original research studies and ensure publication in reputed journals.</li><li>Stay updated on national and international advancements in cancer cytology and molecular diagnostics.</li><li>Present findings to technical committees and contribute to innovations in diagnostic protocols.</li></ul><p><b>3. Training and Education</b></p><ul><li>Clinical Training for Professionals: Provide structured training to doctors, pathologists, and lab personnel on diagnostic use and interpretation of VELscan and DNA Ploidy.</li><li>CME Program Development: Create and deliver Continuing Medical Education (CME) modules for institutional and public platforms.</li><li>On-Site Installation &amp; Client Training: Travel to client locations (hospitals, labs, clinics, Institutes) to install systems and provide hands-on training on sample processing, interpretation, troubleshooting, and workflow optimization</li></ul><p><b>4. Knowledge Dissemination and Communication</b></p><ul><li>Translate complex medical content into simplified formats for marketing, public education, and internal use.</li><li>Contribute to creation of brochures, presentation, videos, and digital content.</li><li>Participate in patient awareness campaigns, health education talks, and community engagement.</li></ul><p>5. Customer Success and Medical Support</p><ul><li>Address medical queries from clients regarding report interpretation and test applications.</li><li>Serve as the key medical contact for labs and hospitals using VELscan and DNA Ploidy systems.</li><li>Build long-term relationships with customers and ensure successful usage of diagnostic platforms.</li></ul><p><b>6. Workshops and Community Engagement</b></p><ul><li>Conduct or participate in diagnostic camps, oral cancer screening events, and field-based</li><li>data collection.</li><li>Lead &quot;Best Practices&quot; workshops and awareness programs for medical professionals and public health partners</li></ul><p><b>Required Qualifications &amp; Skills:</b></p><p><b>Qualifications</b>:</p><ul><li>MDS in Oral and Maxillofacial Pathology</li><li>Expertise in clinical evaluation of OPMD and Oral Cancers</li><li>1-2 years of experience</li><li>Comfortable using computers</li><li>Fresher are welcome provided they can pass our training regimen.</li></ul><p><b>Skills required:</b></p><ul><li>Exceptional Cognitive Ability</li><li>Outstanding Communication &amp; Persuasion Skills</li><li>Passion for Education</li><li>Enthusiasm for Travel &amp; Saving Lives</li><li>Strong Professional Networking Skills</li></ul><p>Job Type: Full-time</p><p>Pay: ₹300,000.00 - ₹600,000.00 per year</p><p>Work Location: In person</p>

Dentist (MDS – Oral Pathology & Microbiology)

Baptist Health

<p></p><div><p>Department: Case Coordination
</p><p>Shift: Day
</p><p>Working Hours: 8-5
</p><p>Summary:<br>
<br>
</p><p>The Case Coordinator II is accountable for the clinical and financial outcome of care for an assigned case load. He/she functions as an advanced practitioner in the role of clinician, educator, researcher, case manager, and advocate. Facilitates the care of observation and inpatients during their hospitalization by managing, coordinating and monitoring resources to achieve optimal level of independence and health for patients and families; clinical outcomes; utilization; service, and financial goals by performing the roles of assessor, planner, facilitator and advocate. The Case Coordinator II uses Continuous Improvement (CI) principles.
</p><div><p>Other information:<br>
<br>
</p><p><b>License &amp; Certification </b>: RN License
<br>
<b>Education </b>: Baccalaureate degree or experience commensurate with a degree. Master's Degree preferred.
<br>
<b>Experience: </b>5 years of appropriate clinical experience (adult Med/Surg). 3 years of supervisory experience preferred. Charge nurse or team leader experience.
<br>
<b>Knowledge, Skills, and Abilities </b>: Knowledge and education, including but not limited to the following; clinical expertise, excellent observation skills, analytical thinking, problem solving, good verbal and written communication, knowledge of adult education principles, research process, change theory, management skills, financial analysis and group process.
</p><p></p><div><p>This job will be authorized 80.00 hours bi-weekly.</p></div></div></div>

Clinical Case Coordinator II

General Dynamics Information Technology

<div><div><div><div><div><p>SHARE</p></div></div></div><div></div><div><p>
REQ#: RQ214393</p><p>
Public Trust: NACI (T1)
</p><p>Requisition Type: Regular
</p><p>Job Description</p><div>
GDIT's Military Health team is hiring a Clinical Research Monitor to support the Office of Regulated Activities (ORA) under the DoW located at Ft. Detrick in Frederick, Maryland.The Office of Regulated Activities (ORA) is a multidisciplinary team of regulatory affairs, compliance, and clinical support professionals dedicated to supporting the USAMRDC mission of developing Food and Drug Administration regulated medical products for the Warfighter. The ORA provides full-service, oversight, and consultation for regulatory, clinical, non-clinical, manufacturing, data management, biostatistics, product technical, safety monitoring. ORA operates in a high-paced environment and seeks individuals who can work independently and take initiative in completing tasks.The CRM will provide clinical trial monitoring to ensure all sponsor required trial monitoring is conducted and all deliverables are provided according to 21 CFR 312 and ICH.This is a hybrid position and will report onsite 2 days a week at Ft. Detrick in Frederick, Maryland. Must reside within commuting distance.HOW YOU WILL MAKE AN IMPACT:<ul><li>
Develop a Clinical Monitoring Plan and monitor single site and multicenter clinical studies both inside and outside the continental United States; when required, conduct centralized monitoring activities.</li><li>
Remote review of electronic source documents, electronic Case Report Forms (CRFs), trends, and metrics in order to identify and mitigate safety and data quality risk issue(s), prepare Clinical Monitoring Reports and file in the sponsor&rsquo;s regulatory file. The monitoring reports shall include the date of activities, description of the activities, and any findings from the activities-Prepare protocol deviations and violation and non-compliance reports</li><li>
Provide remote evaluation of the study data, carried out by a team including central monitors, medical reviewers at a location other than the sites at which the clinical investigation is being conducted and annotate in monitoring reports for the sponsor&rsquo;s regulatory file.</li><li>
Prepare/review calibration and maintenance records, which are records kept at the clinical site that document the calibration and maintenance of all applicable equipment utilized during the execution of the clinical trial including laboratory equipment, and ensure equipment is adequate, current, accessible and annotate this information in monitoring reports for the sponsor&rsquo;s regulatory file.</li><li>
Prepare and/or review shipment records, which include shipping documentation for investigation products, biological samples, and if applicable, other study supplies provided to the clinical sites.</li><li>
Prepare and/or review laboratory sample analysis reports</li></ul>
WHAT YOU&rsquo;LL NEED TO SUCCEED:<ul><li>
Bachelors degree, 4+ year&rsquo;s experience supporting clinical research</li><li>
Experience reviewing electronic source documents, electronic Case Report Forms (CRFs), prepare Clinical Monitoring Reports and file in the sponsor&rsquo;s regulatory file.</li><li>
Experience providing remote evaluation of the study data</li><li>
Experience preparing/reviewing calibration and maintenance records to ensure equipment is adequate, current, accessible and annotate this information in monitoring reports for the sponsor&rsquo;s regulatory file.</li><li>
Experience preparing and/or reviewing shipment records, documentation for investigation products, biological samples, and other study supplies provided to the clinical sites.</li><li>
Must be a US Citizen with the ability to obtain a favorable NACI T1 security investigation prior to start date.</li></ul>
WHAT GDIT CAN OFFER YOU:<ul><li>
Challenging work that makes a real impact on the world around you</li><li>
Internal mobility team dedicated to helping you own your career</li><li>
401K with company match</li><li>
Diverse, highly collaborative teams</li><li>
Professional development, education assistance, certification and training opportunities</li></ul>
#GDITHealth#militaryhealth#GDITLabScienceJobs#GDITFedHealthJobs #GDITPriority
</div></div><div><div><div><p>Work Requirements</p></div></div><div></div><div><div>
Years of Experience<div>
4 + years of related experience</div><ul><li>may vary based on technical training, certification(s), <i>or</i> degree</li></ul></div><div></div><div>
Certification</div><p></p><div>
Travel Required<div>
Less than 10%</div></div><div></div><div>
Citizenship<div>
U.S. Citizenship Required</div></div></div></div></div><div><p>
Salary and Benefit Information</p><div>
The likely salary range for this position is $83,927 - $113,549. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this range.<br>
View information about benefits and our total rewards program.</div><p>
About Our Work</p><div>
We are GDIT. A global technology and professional services company that delivers technology and mission services to every major agency across the U.S. government, defense and intelligence community. Our 30,000 experts extract the power of technology to create immediate value and deliver solutions at the edge of innovation. We operate across over 50 countries worldwide, offering leading capabilities in digital modernization, AI/ML, cloud, cyber and application development. Together with our customers, we strive to create a safer, smarter world by harnessing the power of deep expertise and advanced technology.</div><div>
Join our Talent Community to stay up to date on our career opportunities and events at gdit.com/tc.</div><div><i>
Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans</i></div></div></div>

Clinical Research Monitor

University of Alabama, Birmingham

<div></div><div><div><div><div><div><b>Description</b><div></div><p>
To recruit, schedule and perform follow-up with research participants as protocols dictate. To maintain<br>
current contact information for all past, present and potential study participants along with referring<br>
facilities. To create and execute recruitment strategies based on needs of protocol. May work evenings<br>
depending on study needs.<br>
<b>Key Duties &amp; Responsibilities</b><br>
1. Develops protocol-specific recruitment materials. Prepares study-related folders/packets and<br>
mailings.<br>
2. Contributes to the development of recruitment metrics and analyzes these data to assess status<br>
and effectiveness of efforts. Administers data collection in-person, on phone or by zoom depending<br>
on study protocols. May utilize study-specific systems for data collection and processing needs such<br>
as OnCore, Greenphire or Oracle.<br>
3. Serves as principal source of information for all volunteers, participants, staff, and investigators on<br>
recruitment processes and campaigns. Contributes to the formulation of marketing and<br>
communication plans. May assist in the development of survey instruments.<br>
4. Educates patients on clinical research studies. Pre-screens patients for eligibility for clinical<br>
research studies. Consents or facilitates consent with patients verbally or in-person in clinics,<br>
hospitals, or communities. Maintains a contact list of clinic referrals. Schedules patients for<br>
screening visits. Conducts reminder calls and/or manages rescheduling of potential participants.<br>
Triages participant concerns with managers, directors, and investigators.<br>
5. Identifies, develops and cultivates partnerships with community members. Reaches out to clinics in<br>
the community to inform about studies, request displays and schedule lunch and learns.<br>
6. Attends and reports at regular study meetings with managers, directors and investigators. May<br>
attend study-specific investigator meetings throughout the United States.<br>
7. Performs other duties as assigned.</p><p><b>
Part Time</b><br>
<b>Expected Length of Assignment</b>: 3 months</p><div><br>
</div></div><div><b>
Qualifications</b><div></div><p>
Minimum Requirements<br>
High School Diploma or GED required.</p><p><br>
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.</p><div><br>
</div></div><div><b>
Primary Location</b><b>:</b> Temporary Services</div><div><b>
Job Category</b><b>:</b> UAB Temporary Services</div><div><b>
Organization</b><b>:</b> 114402000 Temporary Services</div><div><b>
Employee Status</b><b>:</b> Temporary</div><div><b>
Shift</b><b>:</b> Day/1st Shift</div><div><b>
Work Arrangement (final schedule to be determined by the department/hiring manager)</b><b>:</b> Onsite</div></div></div></div></div><div></div>

Clinical Research Recruiter

Fuse Energy

<div>
 We are currently seeking a quantitative researcher with a strong background in statistics to join our team. The role will be responsible for developing and implementing models for our energy supply business. As a quant researcher, you will work closely with our engineering team to ensure the accuracy and effectiveness of our models.
 <br/>
 <br/>
 Responsibilities:
 <br/>
 <br/>
 <ul>
  <li>
   Develop and implement models for our energy supply business using Python and other data science tools
  </li>
  <li>
   Identify, analyze, and mitigate credit risk
  </li>
  <li>
   Conduct data analysis and modeling to support risk management decisions
  </li>
  <li>
   Stay current with industry developments and regulations related to credit risk management
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   2+ years of experience as a quantitative researcher or data scientist
  </li>
  <li>
   Strong programming skills in Python and experience with data science tools such as Pandas, NumPy, and SciPy
  </li>
  <li>
   Strong statistical and modeling skills
  </li>
  <li>
   Strong communication and collaboration skills
  </li>
  <li>
   Experience in the energy industry is a plus
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Benefits
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Competitive salary and a stock options sign-on bonus
  </li>
  <li>
   Biannual bonus scheme
  </li>
  <li>
   Fully expensed tech to match your needs!
  </li>
  <li>
   28 days paid annual leave per year including public holiday
  </li>
 </ul>
</div>


Quantitative Researcher

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