Business Analyst

โญ - Featured Role | Apply direct with Data Freelance Hub
This role is for a Business Analyst with 5+ years of experience in life sciences R&D, focusing on clinical research workflows and Medidata Rave. It offers a remote contract position in Gaithersburg, MD, with a competitive pay rate.
๐ŸŒŽ - Country
United States
๐Ÿ’ฑ - Currency
$ USD
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๐Ÿ’ฐ - Day rate
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๐Ÿ—“๏ธ - Date discovered
August 15, 2025
๐Ÿ•’ - Project duration
Unknown
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๐Ÿ๏ธ - Location type
Remote
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๐Ÿ“„ - Contract type
Unknown
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๐Ÿ”’ - Security clearance
Unknown
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๐Ÿ“ - Location detailed
United States
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๐Ÿง  - Skills detailed
#Data Management #Medidata Rave #Agile #DevOps #Documentation #Compliance #Azure DevOps #Business Analysis #Stories #R #Azure
Role description
Hi, Hope you are doing great! You can directly call me at 469-217-5559 & Share resume at Singh.ankita@net2source.com This is 100% Placement Job on urgent Basis. Legal name (First Name, Middle name, and Last Name): Location (City and State): Comfortable to work Remote? Rate Expectation : Phone #: Mobile#: Skype ID: Email address: Visa type: Visa Expiration Date: LinkedIn URL: Please find below the job description. Role Name: Business Analyst with Clinical/R&D Pharma business knowledge Location: Gaithersburg, MD. REMOTE Job Description: We are seeking a skilled and detail-oriented Business Analyst to join our Life Sciences R&D team. The ideal candidate will have hands-on experience in gathering and translating user and functional requirements, with a strong understanding of clinical research workflows, informed consent processes, and electronic data capture systemsโ€”particularly Medidata Rave. Key Responsibilities Collaborate with cross-functional teams to elicit, analyze, and document business and functional requirements for clinical research initiatives. Translate complex business needs into clear user stories, wireframes, and specifications for development teams. Lead workshops and stakeholder interviews to gather insights on informed consent workflows and data capture needs. Develop and maintain documentation such as User Requirement Specifications (URS), Functional Requirement Specifications (FRS), and Data Definition Specifications (DDS) Support the design and implementation of solutions that align with regulatory standards and clinical lifecycle processes Interface with technical teams to ensure seamless integration of Medidata Rave and other tools into clinical trial operations . Contribute to process improvement initiatives by leveraging domain expertise and agile methodologies Required Qualifications Bachelorโ€™s or Masterโ€™s degree in Life Sciences, Information Systems, or related field. 5+ years of experience as a Business Analyst in the life sciences industry, with a focus on R&D. Proven experience with Medidata Rave or similar EDC platforms. Strong understanding of informed consent processes and regulatory compliance in clinical trials. Familiarity with clinical data flow, pharmacovigilance, and patient data management Excellent communication skills with the ability to convey technical concepts to non-technical stakeholders. Experience working in agile environments and using tools like Azure DevOps for backlog and sprint planning 6. Preferred Skills Ability to manage multiple priorities and deliver high-quality outcomes under tight deadlines. Best Regards, Ankita | Talent Acquisition Specialist N2S Global Workforce Solutions Ltd. Global HQ Address โ€“ 270 Davidson Ave, Suite 704, Somerset, NJ 08873, USA Email:-Singh.ankita@net2source.com | Cell : 469-217-5559 |LinkedIn