2026 summer intern - translational pharmacokinetics & pharmacodynamics Jobs in San Francisco

2026 summer intern - translational pharmacokinetics & pharmacodynamics

clinical lab scientist Jobs in San Francisco

clinical lab scientist

clinical research coordinator Jobs in San Francisco

clinical research coordinator

clinical research coordinator (supplements) Jobs in San Francisco

clinical research coordinator (supplements)

researcher engineer/scientist, training Jobs in San Francisco

researcher engineer/scientist, training

clinical trial research scientist

Alignerr

<div>
 <strong>
  Role Overview
  <br/>
  <br/>
 </strong>
 The
 <strong>
  Clinical Trial Research Scientist
 </strong>
 evaluates clinical study protocols, trial designs, endpoints, statistical plans, and study results. This role emphasizes methodological rigor, documentation clarity, and accurate interpretation of safety and efficacy outcomes.
 <br/>
 <br/>
 <strong>
  What You&rsquo;ll Do
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Review clinical trial protocols and identify methodological strengths or gaps
  </li>
  <li>
   Analyze endpoints, inclusion/exclusion criteria, and study controls
  </li>
  <li>
   Interpret trial results and summarize safety and efficacy findings
  </li>
  <li>
   Validate statistical analysis plans for completeness and accuracy
  </li>
  <li>
   Identify operational or scientific risks in trial execution
  </li>
  <li>
   Support recurring evaluations of clinical documentation and study outputs
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Must-Have
  <br/>
  <br/>
 </strong>
 <strong>
  What You Bring
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience in clinical research, biostatistics, or pharmaceutical science
  </li>
  <li>
   Strong understanding of trial methodology and regulatory standards
  </li>
  <li>
   Ability to interpret trial data and communicate findings clearly
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Nice-to-Have
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience with Phase I&ndash;IV trials or specific therapeutic areas
  </li>
 </ul>
</div>


Clinical Trial Research Scientist

UCSF Health

<p></p><div><div><div><div><p>Perform test procedures in Molecular Diagnostics. Responsible for pre-analytical, analytical, and post-analytical processes associated with specimen processing, test performance and reporting test results.<br>
Perform isolation of DNA and RNA from human blood and bone marrow specimens using manual and automated techniques to set-up molecular assays and perform analysis of data. Experience with PCR, qPCR, capillary electrophoresis, and other molecular platforms is preferred.<br>
Transcribe and report test results. Operate laboratory instrumentation &amp; equipment to accurately generate test results.<br>
Initiate troubleshooting of errant laboratory instrumentation &amp; equipment as needed. Follow established quality control procedures and participate in all associated tasks in the section.<br>
<br>
The final salary and offer components are subject to additional approvals based on UC policy.</p><p>
Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.</p><p>
The salary range for this position is $68.81 - $85.71 (Hourly Rate).</p><p>
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html</p></div>
</div><div><p><b>Required Qualifications</b></p>
<div><ul><li>California Clinical Laboratory Scientist license or Clinical Genetics Molecular Biologist license</li><li>
Bachelor of Science degree</li><li>
The flexibility to orient and work at all UCSF Medical Center locations is required</li></ul></div>
</div><div><p><b>Preferred Qualifications</b></p>
<div><ul><li>Recent clinical experience in molecular diagnostics laboratory</li><li>
Previous experience in high-volume clinical laboratory testing
</li><li>Experience with current automation used in the Molecular Diagnostics section</li></ul></div>
</div><div><p><b>License/Certification</b></p>
<div><ul><li>California Clinical Laboratory Scientist license or Clinical Genetics Molecular Biologist license</li></ul></div>
</div><div><p><b>About UCSF</b></p>
<div>At UCSF Health, our mission of innovative patient care, advanced technology and pioneering research is redefining what&rsquo;s possible for the patients we serve &ndash; a promise we share with the professionals who make up our team.
<br>
<br>
Consistently ranked among the top 10 hospitals nationwide by U.S. News &amp; World Report &ndash; UCSF Health is committed to providing the most rewarding work experience while delivering the best care available anywhere. In an environment that allows for continuous learning and opportunities for professional growth, UCSF Health offers the ideal atmosphere in which to best use your skills and talents.</div>
</div><div><p><b>Pride Values</b></p>
<div>UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence &ndash; also known as our PRIDE values.
<br>
<br>
In addition to our PRIDE values, UCSF is committed to equity &ndash; both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at diversity.ucsf.edu
<br>
<br>
Join us to find a rewarding career contributing to improving healthcare worldwide.</div>
</div><div><p><b>Equal Employment Opportunity</b></p>
<div>The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.</div>
</div><div><p><b>Organization</b></p>
<div>Health</div>
</div><div><p><b>Job Code and Payroll Title</b></p>
<div>008940 CLIN LAB SCI
</div></div><div><p><b>Job Category</b></p>
<div>Allied Health, Clinical Labs</div>
</div><div><p><b>Bargaining Unit</b></p>
<div>University Professional and Technical Employees - Health Care Professionals Unit (UPTE-HX)
</div></div><div><p><b>Employee Class</b></p>
<div>Career</div>
</div><div><p><b>Percentage</b></p>
<div>100%</div>
</div><div><p><b>Location</b></p>
<div>San Francisco, CA
</div></div><div><p><b>Campus</b></p>
<div>China Basin (SF)
</div></div><div><p><b>Work Style</b></p>
<div>Fully On-Site</div>
</div><div><p><b>Shift</b></p>
<div>Days</div>
</div><div><p><b>Shift Length</b></p>
<div>8 Hours
</div></div><div><p><b>Additional Shift Details</b></p>
<div>Monday-Friday</div></div></div></div><div></div>

Clinical Lab Scientist

Olema Oncology

<div><div><p>Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.
</p><p>Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you're ready to join us at the edge of something unstoppable, let's make a profound impact together for <b>our patients, for your career, for what's beyond</b>.</p>
<p>
You can view our latest corporate deck and other presentations here.</p></div><p><b>
About the Role &gt;&gt;&gt; Director, Clinical Monitoring Oversight</b></p>
<p>
As the Director, Clinical Monitoring Oversight, reporting to the Senior Director, Clinical Operations, you will provide strategic and operational leadership for global clinical site monitoring activities across Olema's clinical programs. You will ensure that clinical monitoring &ndash; whether by internal teams, through Functional Service Providers (FSPs), or outsourced to Clinical Research Organizations (CROs) &ndash; is executed with high standards of quality and consistency while maintaining compliance with GCP regulations. You will oversee Olema's Clinical Monitoring Oversight Leads, regional monitoring teams, and site performance. As the Director, Clinical Monitoring Oversight, you will develop and implement monitoring oversight strategies and standards for Olema's clinical monitoring execution worldwide&mdash;driving operational excellence, data integrity, and inspection readiness across all trials with an emphasis on risk-based, data driven processes.</p>
<p>
This role is based out of either our Boston, MA or San Francisco, CA office and will require about travel 15% travel.
</p><p>Your work will <i>primarily</i> encompass:</p>
<ul>
<li>Provide strategic direction and operational oversight of all global monitoring activities across Olema's clinical programs</li>
<li>Oversee internal clinical monitoring oversight team and FSP vendor responsible for providing Regional Site Monitoring Leads (RSMLs), ensuring alignment, consistency, and accountability across global regions</li>
<li>Establish and maintain effective governance with the FSP partner, including performance management, risk mitigation, and continuous improvement in monitoring quality and efficiency</li>
<li>Define and implement Olema's monitoring strategy, including risk-based and centralized monitoring approaches in alignment with ICH-GCP and regulatory expectations</li>
<li>Ensure global harmonization of clinical monitoring processes, training, and documentation across programs and regions</li>
<li>Develop and monitor key performance indicators (KPIs) and quality metrics to evaluate site performance, FSP delivery, and regional oversight effectiveness</li>
<li>Collaborate with Clinical Operations, Data Management, Clinical Quality, and Clinical Development to ensure monitoring activities are aligned with program objectives and timelines</li>
<li>Contribute to the development and review of key operational documents, including Monitoring Plans, Oversight Plans, Risk Management Plans, and audit/inspection responses</li>
<li>Proactively assess monitoring risks and implement mitigation strategies to maintain inspection readiness</li>
<li>Lead, manage, and mentor internal monitoring oversight staff, fostering collaboration, accountability, and continuous improvement</li>
<li>Serve as the Monitoring Oversight representative on cross-functional and governance teams, presenting program updates, risks, and mitigation strategies to senior management</li>
<li>Drive innovation and process optimization in monitoring oversight practices, including leveraging technology and data analytics to enhance quality and efficiency</li>
</ul>
<p> <b>Ideal Candidate Profile &gt;&gt;&gt;</b></p>
<p><b>
A love of challenging, important work. </b>We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of <i>knowledge</i>, <i>experience</i>, and <i>attributes</i> for this role.</p>
<p><i>
Knowledge:</i></p>
<ul>
<li>Bachelor's or Master's degree in a scientific discipline or a related scientific field is required</li>
<li>Strong understanding of ICH-GCP, FDA, EMA, and other global regulatory requirements related to monitoring and clinical trial conduct</li>
</ul>
<p> <i>Experience:</i></p>
<ul>
<li>Minimum 12 years of clinical operations experience in the pharmaceutical or biotech industry</li>
<li>Minimum 5 years direct site monitoring experience (qualification, initiation, interim, and close-out visits) with strong understanding of site operations and clinical trial execution</li>
<li>Minimum 5 years in a role providing global monitoring oversight, including oversight of clinical site monitors, FSP/CRO management and oversight, monitoring quality metrics, KPIs, and governance, and a track record of driving performance improvement and corrective action plans</li>
<li>Experience overseeing regional monitoring functions and ensuring alignment across geographically distributed teams</li>
<li>Oncology experience is required
 </li></ul><p><i>Attributes:</i></p>
<ul>
<li>Demonstrated ability to manage FSP or CRO partnerships, including contract governance, KPI development, and issue escalation</li>
<li>Skilled in risk-based monitoring methodologies and the use of oversight tools and systems</li>
<li>Strategic thinker with excellent communication, leadership, and interpersonal skills, with the ability to influence cross-functionally and externally</li>
<li>Strong analytical and problem-solving abilities; adept at managing competing priorities in a fast-paced environment</li>
</ul>
<p>The base pay range for this position is expected to be <b><i>$235,000 - $250,000</i></b> annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.</p>
<p>
#LI-CK1</p><div><p><b>
Important Information </b><b>&gt;&gt;&gt;</b><b>
</b></p><p>We provide <b>equal opportunity to all employees and applicants for employment</b> and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.</p>
<p>
We offer a <b>competitive compensation and benefits package</b>, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.</p>
<p><i>
Please note: Olema doesn't accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.</i></p>
<p><b><i>
Fraud Alert</i></b><i>: </i>We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema's official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.</p></div></div>

Director, Clinical Monitoring Oversight

<div><div><p>Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.
</p><p>Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you're ready to join us at the edge of something unstoppable, let's make a profound impact together for <b>our patients, for your career, for what's beyond</b>.</p>
<p>
You can view our latest corporate deck and other presentations here.</p></div><p><b>
About the Role &gt;&gt;&gt; Senior Director, Biostatistics</b></p>
<p>
As the Senior Director of Biostatistics, reporting to the VP of Biostatistics, you will play an instrumental role in leading the statistical strategy and execution of a pivotal Phase 3 clinical trial and all associated NDA activities. You will leverage your technical expertise to apply and share knowledge of appropriate statistical methods for clinical trial design and data analysis. Additionally, you will collaborate cross-functionally to support the planning, execution, and analysis of the trial.
</p><p>This role is based in either our San Francisco, CA or Cambridge, MA office and will require minimal travel (about 10%).</p>
<p>
Your work will <i>primarily</i> encompass:</p>
<ul>
<li>Lead the biostatistics strategy and execution for a pivotal Phase 3 trial and ISS/ISE, ensuring scientific rigor and global regulatory alignment.</li>
</ul><ul><li>Apply innovative statistical methods to optimize study design, analysis strategies, and data interpretation.</li>
</ul><ul><li>Develop and author key statistical documents.</li>
</ul><ul><li>Lead statistical activities for regulatory submissions and prepare briefing materials for health authority interactions.</li>
</ul><ul><li>Provide statistical input for CSRs, IBs, DSURs, and other study-level and submission documents.</li>
</ul><ul><li>Oversee development of SDTM, ADaM, and TLF deliverables to ensure accuracy and compliance with regulatory and CDISC standards.</li>
</ul><ul><li>Manage CRO statistical activities, including DMC deliverables, to ensure high-quality execution.</li>
</ul><ul><li>Manage and mentor junior statisticians as applicable.</li>
</ul><ul><li>Provide statistical leadership across multiple projects with overlapping timelines, as needed.</li></ul><br>
<p></p>
<p><b>
Ideal Candidate Profile &gt;&gt;&gt;</b></p>
<p><b>
A love of challenging, important work. </b>We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of <i>knowledge</i>, <i>experience</i>, and <i>attributes</i> for this role.</p>
<p><i>
Knowledge:</i></p>
<ul>
<li>Strong understanding of regulatory requirements, industry standards, and guidance documents.</li>
</ul><ul><li>Broad and thorough knowledge of statistical principles and clinical trial methodology, with the ability to apply best practices in oncology study design and analysis.</li>
</ul><ul><li>Comprehensive understanding of RECIST 1.1 guidelines.</li>
</ul><ul><li>Expertise in CDISC standards, including SDTM and ADaM.</li>
</ul><ul><li>Proficiency in SAS and/or R programming.</li>
</ul><ul><li>Demonstrated ability to lead and successfully complete major programs and projects.</li>
</ul><ul><li>Strong analytical, problem-solving, and communication skills.</li>
<li>Experience interacting with regulatory agencies, including the FDA and international health authorities.</li>
</ul>
<p><i>Experience:</i></p>
<ul>
<li>10+ years of experience in the biotech or pharmaceutical industry, with a PhD in Statistics or Biostatistics.</li>
</ul><ul><li>Minimum of 3 years direct leadership experience.</li>
</ul><ul><li>Extensive experience in late-stage oncology drug development, including the design and execution of registrational Phase 3 studies.</li>
</ul><ul><li>Proven experience in regulatory interactions, with a strong track record of NDA or sNDA submissions.</li>
</ul><ul><li>Experience building a biostatistics strategy and execution of a global NDA submission (Phase 3, ISS, ISE)</li>
</ul><ul><li>Demonstrated ability to manage CROs in the conduct and analysis of clinical trials.</li>
</ul><ul><li>Proven ability to represent Biostatistics effectively in multidisciplinary meetings.</li>
</ul><ul><li>Strong history of effective collaboration across cross-functional teams.</li></ul><br>
<p></p>
<p><i>
Attributes:</i></p>
<ul>
<li>Strong leadership skills, including proactive strategic thinking, prioritization, adaptability, conflict resolution, and partnership-building.</li>
</ul><ul><li>Deep statistical expertise and experience overseeing the statistical components of clinical trials.</li>
</ul><ul><li>Ability to develop innovative and creative statistical and technical solutions to complex problems.</li>
</ul><ul><li>Excellent verbal and written communication skills.</li>
</ul><ul><li>Commitment to excellence and consistently delivering high-quality work.</li>
</ul><ul><li>Self-motivated and enthusiastic, with the ability to quickly learn, identify core project challenges, and adapt to evolving requirements in a fast-paced environment.</li>
</ul><ul><li>Possesses impeccable professional ethics, integrity, and judgment.</li>
</ul>
<p>The base pay range for this position is expected to be<b><i> $292,000 - $308,000</i></b><i> </i>annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.</p>
<p>
#LI-MK1</p><div><p><b>
Important Information </b><b>&gt;&gt;&gt;</b><b>
</b></p><p>We provide <b>equal opportunity to all employees and applicants for employment</b> and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.</p>
<p>
We offer a <b>competitive compensation and benefits package</b>, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.</p>
<p><i>
Please note: Olema doesn't accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.</i></p>
<p><b><i>
Fraud Alert</i></b><i>: </i>We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema's official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is olema.com/careers; our LinkedIn page is linkedin.com/company/olema-oncology. Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.</p></div></div>

Senior Director, Biostatistics

Binding Minds

<p><b>ABOUT THE ROLE</b></p><ul><li>Assist in all phases of a matter from case inception through trial or resolution.</li><li>Assist with document collections, document reviews, and document productions.</li><li>Coordinate management of case documents, including organization, review and production of documents.</li><li>Consult with firm&rsquo;s eDiscovery Resource Management team to manage document databases and coordinate electronic discovery proceedings.</li><li>Assist with the preparation of court filings, including cite and fact checking legal briefs, confirming proper Bluebook citation, proofreading, and assembling of exhibits and appendices.</li><li>Assist with depositions, including preparation of witness files, exhibits, notices and subpoenas, and deposition summaries.</li><li>Conduct factual or legal research; examine public records; monitor legislative and administrative proceedings as assigned; locate witnesses; trace documents and other physical evidence.</li><li>Assist with trial preparation and logistics, including preparation of witness files, management of exhibits, setting up trial space, and attending trial, as required.</li></ul><p><b>ABOUT YOU</b></p><ul><li>Bachelor&rsquo;s Degree preferred.</li><li>2 to 5 years relevant experience in practice area or comparable work experience preferred.</li></ul><p>Job Type: Full-time</p><p>Pay: $70,000.00 - $125,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Experience:</p><ul><li>General &amp; commercial litigation: 4 years (Required)</li></ul><p>Work Location: On the road</p>

Litigation Paralegal

Oscar Health

<div><p>Hi, we're Oscar. We're hiring a Senior Data Scientist to join our Data team.</p>
<p>
Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on serving our members. We started Oscar in 2012 to create the kind of health insurance company we would want for ourselves&mdash;one that behaves like a doctor in the family.</p>
<p><b>
About the role:</b></p>
<p>
The Senior Data Scientist, Advanced Risk Modeling, is a senior individual contributor role focused on utilizing advanced machine learning (ML) and artificial intelligence (AI) methodologies on modern ML platforms. This role will build and deploy sophisticated models to help solve complex business problems specifically within Oscar's risk adjustment domain.</p>
<p>
You will report into the Director of Data.</p>
<p><b>
Work Location: </b>This is a remote position, open to candidates who reside in: San Francisco, CA. You will be fully remote; however, our approach to work may adapt over time. Future models could potentially involve a hybrid presence at the hub office associated with your metro area. #LI-Remote</p>
<p><b>
Pay Transparency: </b>The base pay for this role is: $158,400- $207,900 per year. You are also eligible for employee benefits, participation in Oscar's unlimited vacation program, company equity grants, and annual performance bonuses.</p>
<p><b>
Responsibilities:</b></p>
<ul>
<li><p>Conduct in-depth data analysis and advanced feature engineering using large, complex healthcare datasets to create robust predictors.</p>
</li>
<li><p>Design, develop, and validate advanced ML/AI models (e.g., regression/classification, deep learning, NLP, gradient boosting, LLM experimentations) to solve complex clinical and business problems within the risk adjustment domain.</p>
</li>
<li><p>Leverage modern ML Ops platforms (e.g., Vertex AI) and data science best practices to efficiently train, test, deploy, and maintain production-level models.</p>
</li>
<li><p>Build and maintain the supporting data systems, analytics, and monitoring infrastructure required for complex, production-level AI/ML systems.</p>
</li>
<li><p>Research, develop, and evaluate new AI applications using cutting-edge techniques, including LLM models and agentic frameworks, to solve critical business challenges in risk adjustment.</p>
</li>
<li><p>Work closely with business stakeholders, engineering teams, and product managers to gain a deep understanding of business operations and technical systems.</p>
</li>
<li><p>Build strong partnerships to foster close, effective integrations between data science, engineering, product, and business units.</p>
</li>
<li><p>Partner with leaders to identify high-impact opportunities, translate complex business challenges into data science solutions, and ensure successful model implementation within business workflows.</p>
</li>
</ul><p><b>Requirements:</b></p>
<ul>
<li><p>4+ years of industry or other quantitative technical fields (which may include academia).</p>
</li>
<li><p>3+ years of work experience working with SQL, R, and/or Python to query, manipulate and analyze data</p>
</li>
<li><p>3+ years experience building data models, using more advanced analytics methods, statistical modeling, and/or data processing</p>
</li>
</ul><p><b>Bonus points:</b></p>
<ul>
<li><p>Advanced degree in a quantitative or technical field</p>
</li>
<li><p>Experience in the healthcare, finance and/or insurance industries</p>
</li>
</ul><div><p>This is an authentic Oscar Health job opportunity. Learn more about how you can safeguard yourself from recruitment fraud here.</p>
<p>
At Oscar, being an Equal Opportunity Employer means more than upholding discrimination-free hiring practices. It means that we cultivate an environment where people can be their most authentic selves and find both belonging and support. We're on a mission to change health care - an experience made whole by our unique backgrounds and perspectives.</p>
<p><b>
Pay Transparency: </b>Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience. Full-time employees are eligible for benefits including: medical, dental, and vision benefits, 11 paid holidays, paid sick time, paid parental leave, 401(k) plan participation, life and disability insurance, and paid wellness time and reimbursements.</p>
<p><b>
Artificial Intelligence (AI): </b>Our AI Guidelines outline the acceptable use of artificial intelligence for candidates and detail how we use AI to support our recruiting efforts.</p>
<p><b>
Reasonable Accommodation: </b>Oscar applicants are considered solely based on their qualifications, without regard to applicant's disability or need for accommodation. Any Oscar applicant who requires reasonable accommodations during the application process should contact the Oscar Benefits Team (accommodations@hioscar.com) to make the need for an accommodation known.</p>
<p><b>
California Residents:</b> For information about our collection, use, and disclosure of applicants' personal information as well as applicants' rights over their personal information, please see our Privacy Policy.</p></div></div>

Senior Data Scientist, Advanced Risk Modeling

University of California - San Francisco

<p></p><div><div><div><div>Coordinator will perform independently or with general direction at the fully operational journey level of the<br>
series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor in<br>
the Department of Surgery as part of the Clinical Research Core. Under the Clinical Research Core, the Clinical Research will be assigned studies across the 7 divisions in the department based on Principal Investigator needs; may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.<br>
<br>
Incumbent&rsquo;s duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and<br>
manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist the Clinical<br>
Research Supervisor with study start up activities, and assist Clinical Research Supervisor and/or PI with oversight of<br>
other research staff; manage Investigator&rsquo;s protocols in the Committee on Human Research online system, as<br>
well as renewals and modifications of protocol applications and the implementation of new studies; participate in<br>
the review and writing of protocols to ensure institutional review board approval within University compliance;<br>
help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and<br>
maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study<br>
initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal<br>
and external audits or reviews of study protocols; and perform other duties as assigned.<p><br>
The final salary and offer components are subject to additional approvals based on UC policy.</p><p>
Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.</p><p>
The salary range for this position is $34.32 - $55.19 (Hourly Rate).</p><p>
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html</p></div>
</div><div><p><b>Department Description</b></p>
<div>The mission of the UCSF Department of Surgery is threefold: to develop the next generation of leaders in surgery; to provide outstanding quality clinical care that is cost effective, yet compassionate; and to make significant advances in scientific knowledge and clinical practice through basic and clinical research. The Department is comprised of multiple divisions and sections and our surgeons provide care at locations throughout the greater San Francisco Bay Area and beyond. Our Residents and Fellows also play a critical role in Department&rsquo;s success. The Department of Surgery Chair&rsquo;s Office is an extremely high profile, fast paced environment with a very diverse range of contacts and needs which require an immediate and accurate response, handled with confidentiality, and while staying compliant. The Chair's Office is responsible for management, direction and oversight of over 400 faculty (clinical and research), trainees and staff personnel.</div>
</div><div><p><b>Required Qualifications</b></p>
<ul><li>HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.</li><li>Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions and companies; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.</li><li>Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines.</li></ul>
</div><div><p><b>Preferred Qualifications</b></p>
<ul><li>Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system.</li><li>Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.</li><li>Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals</li><li>Experience with electronic medical records.</li><li>Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms.</li><li>Experience applying the following regulations and guidelines:</li></ul>
Good Clinical Practice Guidelines<br>
Health Information and Accountability Act (HIPAA)<br>
The Protection of Human Research Subjects<br>
CHR regulations for recruitment and consent of research subjects<br>
Effective Cash Handling Procedures<br>
Environmental Health and Safety Training<br>
Fire Safety Training<br>
<ul><li>BA/BS with biology coursework included</li></ul>
</div><div><p><b>About UCSF</b></p>
<div>The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world&rsquo;s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.</div>
</div><div><p><b>Pride Values</b></p>
<div>UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence &ndash; also known as our PRIDE values.
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In addition to our PRIDE values, UCSF is committed to equity &ndash; both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at diversity.ucsf.edu
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Join us to find a rewarding career contributing to improving healthcare worldwide.</div>
</div><div><p><b>Equal Employment Opportunity</b></p>
<div>The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.</div>
</div><div><p><b>Organization</b></p>
<div>Campus</div>
</div><div><p><b>Job Code and Payroll Title</b></p>
<div>009335 CLIN RSCH CRD
</div></div><div><p><b>Job Category</b></p>
<div>Research and Scientific</div>
</div><div><p><b>Bargaining Unit</b></p>
<div>University Professional Technical Employees &ndash; Research Support Professionals Unit (UPTE-RX)
</div></div><div><p><b>Employee Class</b></p>
<div>Career</div>
</div><div><p><b>Percentage</b></p>
<div>100%</div>
</div><div><p><b>Location</b></p>
<div>San Francisco, CA
</div></div><div><p><b>Campus</b></p>
<div>Parnassus Heights (SF)
</div></div><div><p><b>Work Style</b></p>
<div>Fully On-Site</div>
</div><div><p><b>Shift</b></p>
<div>Days</div>
</div><div><p><b>Shift Length</b></p>
<div>8 Hours
</div></div><div><p><b>Additional Shift Details</b></p>
<div>Mon-Fri, 8-5, occasional after work hours</div></div></div></div><div></div>

Clinical Research Coordinator

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