Research Associate I

Scribe Therapeutics is a molecular engineering company focused on creating best-in-class in vivo therapies that permanently treat the underlying cause of disease.Founded by CRISPR inventors and leading molecular engineers Benjamin Oakes, Brett Staahl, David Savage, and Jennifer Doudna, Scribe is overcoming the limitations of current genome editing...

Job Title: Clinical Research Associate - B Location: Alameda, CA (94502) Shift – 8:00am to 5:00pm Duration: 6 Months with possible extension Payrate starts at $55/hr on W2 Job Responsibilities: Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH...

Job Title: Clinical Research Associate - B Location: Alameda, CA (94502) Shift – 8:00am to 5:00pm Duration: 6 Months with possible extension Payrate starts at $55/hr on W2 Job Responsibilities: Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH...

Job DescriptionSeeking for an experienced Clinical Research Associate who will be responsible for providing Clinical Research support for a biotech company. Under the direction of supervisor or designee, this position will serve as support for the clinical study team.Essential Duties And ResponsibilitiesParticipate and assist in design and preparation of...

CONTRACTMUST HAVES:A BS/BA in Bioengineering, Cell or Molecular Biology, Synthetic Biology, or related discipline3+ years wet lab research experience requiredExperience with animal handling and dosing (IV, IP, SC, OP, etc.)Job Overview:We are seeking a highly creative, passionate, and motivated individual to join us in our quest to develop the next...

CONTRACTMUST HAVES:A BS/BA in Bioengineering, Cell or Molecular Biology, Synthetic Biology, or related discipline3+ years wet lab research experience requiredExperience with animal handling and dosing (IV, IP, SC, OP, etc.)Job Overview:We are seeking a highly creative, passionate, and motivated individual to join us in our quest to develop the next...

CONTRACTMUST HAVES:A BS/BA in Bioengineering, Cell or Molecular Biology, Synthetic Biology, or related discipline3+ years wet lab research experience requiredExperience with animal handling and dosing (IV, IP, SC, OP, etc.)Job Overview:We are seeking a highly creative, passionate, and motivated individual to join us in our quest to develop the next...

at Scribe Therapeutics Alameda, California Our mission is to engineer best-in-class CRISPR therapies that will permanently treat the underlying cause of disease in vivo.Scribe uses holistic molecular engineering to design, evolve, build and apply exclusive CRISPR technologies with enhanced therapeutic attributes for in vivo use.Scribe Therapeutics is seeking...

CONTRACTMUST HAVES:A BS/BA in Biology, or closely related field with 10+ years of lab experience in in-vivo pharmacology and/or bioanalysis in pharmaceutical environments5+ year experience working with rodents, especially miceJob Overview:We are seeking a highly creative, passionate, and motivated individual to join us in our quest to bring the next...

Job DescriptionJob Description·         Must have a minimum of 2 years experience with "clinical research monitoring".·         Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study...

CONTRACTMUST HAVES:A BS/BA in Bioengineering, Cell or Molecular Biology, Synthetic Biology, or related discipline with 2+ years wet lab research experience requiredExperience with mammalian cell and bacterial culture, molecular cloning and common bioassays requiredExpertise in use of mammalian cell reporter systems, screening in human cells, and readout by...

CONTRACTMUST HAVES:A BS/BA in Bioengineering, Cell or Molecular Biology, Synthetic Biology, or related discipline with 2+ years wet lab research experience requiredExperience with mammalian cell and bacterial culture, molecular cloning and common bioassays requiredExpertise in use of mammalian cell reporter systems, screening in human cells, and readout by...

The Opportunity The Associate Clinical Research III 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.  What You'll Work On The incumbent may be...

Job DescriptionJob DescriptionThe CRAII/Sr. CRA 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.Essential Duties and Responsibilities: The incumbent may be...

**PRINCIPAL RESPONSIBILITIES**: Member Services Representatives are under the direction of a Member Services Supervisor, Manager and Director, and service our members through our call center as well assisting other departments with responses to member issues by initiating communication between departments to ensure action, cooperation, and compliance of...

**PRINCIPAL RESPONSIBILITIES**: Under the direction of the Manager Vendor Management, the Vendor Analyst 1 supports the organization in effective vendor monitoring to increase vendor value to the organization. Principal responsibilities include: - Responsible for purchasing all products and services greater than $400 and less than $25,000. - Check routine...

Job DescriptionJob Description·         Emerging Regulations team- manages regulations and works with cross function teams.·         Regulations can be very narrow and specific.·         Analytical, proactive, communication skills, must do research and prep work to understand regulations before meetings with...

**PRINCIPAL RESPONSIBILITIES**: The Provider Data Coordinator I, under general supervision from the Supervisor, Network Data Validation will verify, change and update provider data for accuracy. Provider data will be entered into multiple systems including but not limited to HealthSuite, Excel spreadsheets, and the Provider Repository. **Principal...

The Opportunity The Clinical Manager is responsible for managing and meeting the objectives of clinical projects including but not limited to New Technology Assessments (NTA). Internally interfaces with data management, biostatistics, regulatory, clinical research associates, trial coordinators, field clinical specialists, functional management,...

PRINCIPAL RESPONSIBILITIES: Under the general supervision of the Manager, Claims Operation Support, the principal responsibilities of the Claims Specialist include: Audit Activities: Audit a designated percentage of all daily processing production for assigned staff members (including errors from claims pricing, adjudication, adjustments, member bill...