Clinical Programmer jobs in Oakland, CA

Clinical Programmer evaluates, develops, and maintains clinical database and analyzes clinical data. Codes, tests and documents databases. Being a Clinical Programmer performs data validation and develops algorithms for data management, typically using SAS programming language. May require a bachelor's degree. Additionally, Clinical Programmer typically reports to a supervisor or manager. The Clinical Programmer works on projects/matters of limited complexity in a support role. Work is closely managed. To be a Clinical Programmer typically requires 0-2 years of related experience. (Copyright 2024 Salary.com)

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Clinical Research Associate II
  • Advanced Clinical
  • Alameda, CA FULL_TIME
  • OVERVIEW
    We are currently searching for a skilled professional to join a well-known client's team as a Clinical Research Associate II in Alameda, CA. The Clinical Research Associate II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity.


    RESPONSIBILITIES
    The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
    * Conduct single or multi-center medical device clinical studies.
    * Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items.
    * Participate in study start up activities.
    * Responsible for shipping study devices and supplies to clinical sites and performing study device accountability.
    * Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures and applicable regulatory requirements.
    * Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.
    * Maintain and audit Trial Master File to ensure inspection readiness.
    * Perform review of clinical data listings for completeness and accuracy, and escalate issues to the Clinical Operations Manager as needed*
    * Participate in cross-functional clinical team(s) in the planning and execution of clinical trials.
    * Proactively and effectively communicate the status of clinical studies to management.
    * Ensures quality delivery of study deliverables within agreed budgets and timelines.
    * Participate in the interim and final reviews of study data in preparation of regulatory submissions.
    * Involved in the preparation of all applicable documents required for the conduct of the study (such as Trial Master File (TMF), Clinical Protocols and Reports).
    * May interact with RA/QA in responding to audits and FDA inquiries.

    EDUCATION
    * BS degree in life sciences or equivalent with minimum 5 years of related experience, or MS degree in life sciences or equivalent with minimum 3 years of experience, or PhD with 2 years of experience.

    EXPERIENCE
    * Must have 5 years of relevant experience in site monitoring, clinical project management, clinical trial practices and regulations.
    * Experience in conducting medical device and/or in-vitro diagnostics studies. Pharmaceutical background may also be considered.

    To be a best-fit your strengths must include:
    * Demonstrated excellence in teamwork, shared mindset for success, stellar interpersonal and communication skills including building rapport with team members, peers, and management.
    * Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis; and data reporting and interpretation.
    * Must have a demonstrated ability to solve problems with innovative solutions along with strong project management and organizational skills to deliver projects on time and on budget.
    * Able to manage numerous projects/conflicting priorities, and to be flexible when priorities change.
    * Working knowledge of GCP, Clinical and Regulatory Affairs.
    * Flexibility in daily activities.
    * Proficient with Microsoft Suite.

    Travel Requirements

    * Must be able to travel 30-50%


    About Advanced Clinical

    Advanced Clinical is an award-winning clinical development organization that provides global services including CRO, Functional Support, Quality & Validation, Patient Recruitment and Retention, and Strategic Talent Acquisition solutions for pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Our mission is to deliver a truly better clinical experience for our clients and candidates. To learn more about Advanced Clinical which has been named to Chicago Tribune's Top Workplaces, Chicago's Best and Brightest Companies, and Best of Staffing Talent & Client, visit http://www.advancedclinical.com.

    Regarding your application
    Please know that every completed application is carefully reviewed by the Advanced Clinical recruitment team. We understand the time commitment that is needed to prepare an application, so we respect your effort by thoughtfully reviewing and responding to each application. In return, we ask for your patience as careful review takes time, and we may not be able to respond to every application immediately.

    It is Advanced Group's practice not to discriminate against any employee or applicant because of sex, race, color, age, national origin, religion, gender, gender identity/expression, sexual orientation/sexual preference, pregnancy/maternity, genetic information, marital status, physical/mental disability, medical condition, military/veteran status, or any other basis protected by applicable federal, state, or local law. If you have a disability or handicap and would like us to accommodate you in any reasonable way, please inform your recruiter so that we can discuss the appropriate alternatives available.

     

  • 1 Month Ago

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Pharmacy Clinical Coordinator
  • Clinical Management Consultants
  • San Leandro, CA FULL_TIME
  • A prestigious 100 patient bed hospital in Northern California is searching for a highly motivated and experienced PGY1 and Utilization Review Clinical Pharmacy Coordinator to join their dynamic health...
  • 24 Days Ago

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Psychological Clinical Trial Rater
  • Sunwise Clinical Research
  • Lafayette, CA PART_TIME,CONTRACTOR
  • Full Job Description Looking for a Clinical Psychology Professional will administer psychological efficacy scales, conduct interviews, adhere to study protocols and who will bring excellent patient ca...
  • 13 Days Ago

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Labor and Delivery Clinical Educator
  • Clinical Management Consultants
  • Walnut Creek, CA FULL_TIME
  • An exciting opportunity has opened at a hospital located in Northern California for a Labor and Delivery Nurse Educator. A three time “Women’s Choice Award” Winning Hospital for Obstetrics that is nat...
  • 1 Month Ago

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Clinical Coordinator for Drug Utilization Management
  • Clinical Management Consultants
  • Walnut Creek, CA FULL_TIME
  • A prestigious 100 patient bed hospital in Northern California is searching for a highly motivated and experienced Clinical Coordinator to join their dynamic healthcare team. This is an exceptional opp...
  • 5 Days Ago

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Critical Care Clinical Nurse Specialist
  • Clinical Management Consultants
  • San Leandro, CA FULL_TIME
  • A highly respected hospital in the Bay Area is actively looking for a Critical Care Clinical Nurse Specialist to join its team! This well-respected, 350 bed, multi-award-winning healthcare organizatio...
  • 6 Days Ago

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0 Clinical Programmer jobs found in Oakland, CA area

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Senior Medical Director, Clinical Development
  • Meet
  • 🌟 Join Our Innovative Medical Team: Senior Medical Director, Oncology 🌟 Are you ready to take your career to the next ...
  • 3/28/2024 12:00:00 AM

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Executive Director, Clinical Development, Solid Tumors
  • BeiGene
  • Emeryville, CA
  • **General Description:** The Executive Director, Clinical Development will effectively lead BeiGene clinical assets thro...
  • 3/26/2024 12:00:00 AM

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Vice President, Statistical and Clinical Programming
  • Exelixis Inc.
  • Alameda, CA
  • SUMMARY/JOB PURPOSE: The VP, Statistical and Clinical Programming, leads the organization responsible for developing, va...
  • 3/26/2024 12:00:00 AM

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Vice President of Clinical Development, Rare Disease
  • Recursion
  • Milpitas, CA
  • Your work will change lives. Including your own. The Impact You'll Make You will join an innovative and passionate clini...
  • 3/25/2024 12:00:00 AM

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VP/SVP, Clinical Development
  • Bayside Solutions
  • Fremont, CA
  • VP/SVP, Clinical Development Direct Hire Fulltime Role Salary Range: $300,000 - $400,000 per year Location: Redwood City...
  • 3/24/2024 12:00:00 AM

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Resume Drop - Clinical Development (Clinical Operations, Regulatory Affairs, Project Management, Clinical Development)
  • NGM Biopharmaceuticals, Inc.
  • South San Francisco, CA
  • Don't see what you're looking for but are interested in positions related to Clinical Development? Apply here to submit ...
  • 3/24/2024 12:00:00 AM

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Senior Manager / Associate Director of Clinical Data Management
  • Caribou Biosciences Inc.
  • Berkeley, CA
  • Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing ...
  • 3/24/2024 12:00:00 AM

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Senior Clinical Research Scientist
  • Caribou Biosciences, Inc.
  • Berkeley, CA
  • Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing ...
  • 3/24/2024 12:00:00 AM

Oakland is in the eastern region of the San Francisco Bay. In 1991 the City Hall tower was at 37°48′19″N 122°16′21″W / 37.805302°N 122.272539°W / 37.805302; -122.272539 (NAD83). (The building still exists, but like the rest of the Bay Area, it has shifted northwest perhaps 0.6 meters in the last twenty years.) The United States Census Bureau says the city's total area is 78.0 square miles (202 km2), including 55.8 square miles (145 km2) of land and 22.2 square miles (57 km2) (28.48 percent) of water. Oakland's highest point is near Grizzly Peak Blvd, east of Berkeley, just over 1,760 feet (...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Programmer jobs
$78,230 to $99,195
Oakland, California area prices
were up 4.5% from a year ago

Clinical Programmer in Santa Ana, CA
A clinical programmer works with a staff during clinical trial testing, quite often in the medical field.
December 12, 2019
Clinical Programmer in Austin, TX
Created SAS datasets of clinical data from clinical databases; create status and efficacy datasets; create project specific macros and formats; load client data from other platforms and other software packages; prepared data to be sent to clients.
December 11, 2019
Clinical Programmer in Greenville, MS
Responsibilities shown on sample resumes for this position include reviewing shell data displays for consistency of CRF, importing raw data to SAS datasets, and converting clinical study datasets to conform with CDISC/SDTM standards.
January 30, 2020