Senior Clinical Research Associate Job at Software Guidance & Assistance, Inc. (SGA, Inc.), Boston, MA

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  • Software Guidance & Assistance, Inc. (SGA, Inc.)
  • Boston, MA

Job Description

Software Guidance & Assistance, Inc., (SGA), is searching for an Senior Clinical Research Associate for a Contract assignment with one of our premier Clinical clients in Boston, MA .

Position requires heavy travel to site locations in Minnesota, New Jersey and Illinois . Willing to accept candidates residing anywhere in the US, as long as they can meet the travel expectations and work EST hours to attend daily staff meetings.

  • Responsibilities :Ability to prioritize workload and manage multiple protocols
  • Contribute to the identification of new sites for clinical trials
  • Implement complete site management including monitoring visits and regulatory assessment
  • Resolve technical and content issues to achieve timely database lock targets
  • Negotiate investigator remuneration and prepare financial contracts
  • Implement site close-out activities and generate site close-out report
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  • Responsible for medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements;
  • Required Skills :Must have experience working in clinical trials at CROs , site management experience. Contractor will be expected to take on role as primary contact at site locations and aid with day to day issue resolution
  • Must have 3+ years experience as a CRA from a CRO background
  • Minimum 3 years prior monitoring experience with global trials
  • Minimum 2 years experience with direct interim monitoring experience including SDV (Source Document Verification), SDR (Source Data Review) and MRR (Medical Record Review) with respect to eligibililty (in/ex) criteria. and preferably in a remote environment
  • Must have an In-depth knowledge of FDA regulations and ICH/GCP guidelines
  • CCRA or SOCRA certified - highly preferred
  • Must be familiar and adept with managing fully decentralized studies

SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at .

SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company EEO page to request an accommodation or assistance regarding our policy.

Job Tags

Contract work, For contractors, Interim role, Remote job,

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