In this role you will work closely with the Biostatistics, Programming, and Clinical Operations ... Proficient in web-based Electronic Data Capture (such as Medidata Rave and other clinical data ...
New
In this role you will work closely with the Biostatistics, Programming, and Clinical Operations ... Proficient in web-based Electronic Data Capture (such as Medidata Rave and other clinical data ...
New
In this role you will work closely with the Biostatistics, Programming, and Clinical Operations ... Proficient in web-based Electronic Data Capture (such as Medidata Rave and other clinical data ...
New
Deep expertise in EDC systems (Medidata Rave preferred) and clinical data standards (CDISC CDASH/SDTM, ICH GCP E6(R3), 21 CFR Part 11) * Proven track record managing CRO and third‑party DM vendor ...
Deep expertise in EDC systems (Medidata Rave preferred) and clinical data standards (CDISC CDASH/SDTM, ICH GCP E6(R3), 21 CFR Part 11) * Proven track record managing CRO and third‑party DM vendor ...
In this role you will work closely with the Biostatistics, Programming, and Clinical Operations ... Proficient in web-based Electronic Data Capture (such as Medidata Rave and other clinical data ...
New
In this role you will work closely with the Biostatistics, Programming, and Clinical Operations ... Proficient in web-based Electronic Data Capture (such as Medidata Rave and other clinical data ...
New
Deep expertise in EDC systems (Medidata Rave preferred) and clinical data standards (CDISC CDASH/SDTM, ICH GCP E6(R3), 21 CFR Part 11) * Proven track record managing CRO and third-party DM vendor ...
Quick apply
Deep expertise in EDC systems (Medidata Rave preferred) and clinical data standards (CDISC CDASH/SDTM, ICH GCP E6(R3), 21 CFR Part 11) * Proven track record managing CRO and third-party DM vendor ...
Redmond, WA · On-site
$190K - $250K/yr
Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical ... Minimum 10 years of clinical data management experience within the pharmaceutical, biotechnology ...
Redmond, WA · On-site
$190K - $250K/yr
Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical ... Minimum 10 years of clinical data management experience within the pharmaceutical, biotechnology ...
The company integrates deep protein engineering expertise and has established collaborations with ... management. * Oversee and provide hands-on review of Medidata Rave eCRF design, database build ...
The company integrates deep protein engineering expertise and has established collaborations with ... management. * Oversee and provide hands-on review of Medidata Rave eCRF design, database build ...
The company integrates deep protein engineering expertise and has established collaborations with ... management. * Oversee and provide hands-on review of Medidata Rave eCRF design, database build ...
The company integrates deep protein engineering expertise and has established collaborations with ... management. * Oversee and provide hands-on review of Medidata Rave eCRF design, database build ...
$121K - $202K/yr
... by Clinical Programming and Biostatistics. Key Responsibilities: • Lead the development ... Vendor Management to ensure third-party providers adhere to company data standards from study ...
$121K - $202K/yr
... by Clinical Programming and Biostatistics. Key Responsibilities: • Lead the development ... Vendor Management to ensure third-party providers adhere to company data standards from study ...
San Francisco, CA · On-site
$240K - $275K/yr
Summary Directs planning and execution of clinical trial data management activities including CRF/eCRF design, database development, validation programming, discrepancy management, and database ...
San Francisco, CA · On-site
$240K - $275K/yr
Summary Directs planning and execution of clinical trial data management activities including CRF/eCRF design, database development, validation programming, discrepancy management, and database ...
Waltham, MA · On-site
$143K - $169K/yr
... Rave, Veeva Vault) to validate datasets, specifications, and vendor artifacts. The role will ... Partner with Data Management, Statistics, and vendors to review and validate clinical data ...
Waltham, MA · On-site
$143K - $169K/yr
... Rave, Veeva Vault) to validate datasets, specifications, and vendor artifacts. The role will ... Partner with Data Management, Statistics, and vendors to review and validate clinical data ...
Kingston, NJ · On-site
$109K - $149K/yr
Lead and oversee end-to-end clinical data management activities across assigned studies and projects. * Serve as data management subject matter expert, providing strategic input into study planning ...
Kingston, NJ · On-site
$109K - $149K/yr
Lead and oversee end-to-end clinical data management activities across assigned studies and projects. * Serve as data management subject matter expert, providing strategic input into study planning ...
Works with the Head of Statistical Programming & CDS to manage departmental budget and execute resource planning across multiple projects * Works with the Director of Clinical Data Science to provide ...
Works with the Head of Statistical Programming & CDS to manage departmental budget and execute resource planning across multiple projects * Works with the Director of Clinical Data Science to provide ...
The Director of Clinical Data Management will be responsible for leading data management activities ... Medidata Rave Veeva Vault CDMS) required; working familiarity with data review, visualization, and ...
The Director of Clinical Data Management will be responsible for leading data management activities ... Medidata Rave Veeva Vault CDMS) required; working familiarity with data review, visualization, and ...
Princeton, NJ · On-site
$109K - $149K/yr
Lead and oversee end-to-end clinical data management activities across assigned studies and projects. * Serve as data management subject matter expert, providing strategic input into study planning ...
Princeton, NJ · On-site
$109K - $149K/yr
Lead and oversee end-to-end clinical data management activities across assigned studies and projects. * Serve as data management subject matter expert, providing strategic input into study planning ...
$241K - $292K/yr
Strong knowledge and experience of EDC systems (Medidata RAVE or Veeva). Solid knowledge of GCP ... Senior Director, Clinical Data Management
$241K - $292K/yr
Strong knowledge and experience of EDC systems (Medidata RAVE or Veeva). Solid knowledge of GCP ... Senior Director, Clinical Data Management
$241K - $292K/yr
Strong knowledge and experience of EDC systems (Medidata RAVE or Veeva). * Solid knowledge of GCP ... Senior Director, Clinical Data Management
$241K - $292K/yr
Strong knowledge and experience of EDC systems (Medidata RAVE or Veeva). * Solid knowledge of GCP ... Senior Director, Clinical Data Management
Provide expertise and contribute to the strategy and development of the Clinical Data Management ... Proficient in Medidata RAVE and other EDC platforms; programming experience is a plus * Experience ...
Provide expertise and contribute to the strategy and development of the Clinical Data Management ... Proficient in Medidata RAVE and other EDC platforms; programming experience is a plus * Experience ...
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
Redmond, WA · On-site
$90K - $130K/yr
Manage and continually improve the Spotfire analytics environment, ensuring data integrity ... Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial ...
Redmond, WA · On-site
$90K - $130K/yr
Manage and continually improve the Spotfire analytics environment, ensuring data integrity ... Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial ...
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
Clinical Data Management (CDM) supports drug discovery, development and marketed products across Gilead by ensuring the accurate and timely acquisition, analysis and reporting of diverse clinical ...
$24.76 - $31.84
3% of jobs
$31.84 - $38.92
4% of jobs
$38.92 - $46
9% of jobs
$46 - $53.08
5% of jobs
$54.30 is the 25th percentile. Wages below this are outliers.
$53.08 - $60.16
17% of jobs
The median wage is $63.26 / hr.
$60.16 - $67.24
25% of jobs
$71.78 is the 75th percentile. Wages above this are outliers.
$67.24 - $74.32
17% of jobs
$74.32 - $81.40
9% of jobs
$81.40 - $88.48
6% of jobs
$88.48 - $95.56
2% of jobs
$95.56 - $102.64
1% of jobs
$24
$64
$102
For Clinical Data Management Rave Programmer jobs, the most frequently searched job titles are:

Remote
Full-time
Medical, Dental, Vision, Life, PTO
Posted 3 days ago
New
8.9
Based on 12 frontline employees who took The Breakroom Quiz
We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.
Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.
We are seeking a highly motivated individual to join us as a Senior Data Management Associate. In this role you will work closely with the Biostatistics, Programming, and Clinical Operations teams. This role will be a hands-on resource, reporting to the Senior Manager, Clinical Data Management.
The Senior Data Management Associate will be responsible for overseeing all aspects of clinical data management studies from start-up to close-out for Kite's clinical development programs. The Senior Data Management Associate will also work with Clinical Operations, Safety, and Regulatory as necessary. In this role you follow data management processes and understand the downstream implications of deviations from processes.
Responsibilities (include but are not limited to):
Basic Qualifications
Preferred Qualifications
For additional benefits information, visit:
https://www.gilead.com/careers/compensation-benefits-and-wellbeing
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma.
Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability,genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contactApplicantAccommodations@gilead.com for assistance.
For more information about equal employment opportunity protections, please view the'Know Your Rights' poster.
NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.
Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.
Please apply via the Internal Career Opportunities portal in Workday.
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Scientific research and development services
10,000+ Employees
Foster City, CA, US
1987