Clinical Implementation Specialist

2 days ago


Bengaluru, Karnataka, India Medable, Inc Full time ₹ 6,00,000 - ₹ 12,00,000 per year

Medable's mission is to get effective therapies to patients faster. We provide an end-to-end, cloud-based platform with a flexible suite of tools that allows patients, healthcare providers, clinical research organizations and pharmaceutical sponsors to work together as a team in clinical trials. Our solutions enable more efficient clinical research, more effective healthcare delivery, and more accurate precision and predictive medicine. Our target audiences are patients, providers, principal investigators, and innovators who work in healthcare and life sciences.

Our vision is to accelerate the path to human discovery and medical cures. We are passionate about driving innovation and empowering consumers. We are proactive, collaborative, self-motivated learners, committed, bold and tenacious. We are dedicated to making this world a healthier place.

1. Responsibilities
  • Coordinate the overall Solutions Design process ensuring that the clinical protocols are appropriately mapped to software solutions efficiently, accurately and within project scope.
  • In-depth knowledge of Medable's software, technology, and processes to be able to guide a client to the best use of Medable's platform to meet their needs therapeutic areas meetings.
  • Develop and communicate design best practices for specific.
  • Participate in providing input related to Sales to Service, Kick-Off, Solutions Overview, Specification Review, and Software Review.
  • Develop supporting documentation to streamline software design and configuration. 
  • Leads and executes the end-to-end technical implementation of Medable's products for customer accounts; including configuration and customization of Medable's products, conducting technical testing, quality assurance, and troubleshooting. Serves as a platform expert.
  • Manages technical implementation releases, including timelines, technical milestones, and deliverables. Ensure projects are completed on time, within scope, and meet both technical and customer expectations.
  • Represents the voice of the customer within the product organization by providing actionable technical insights, feedback, and feature requests to Medable's product development teams.
  • Collaborates closely with product teams to translate technical customer feedback into product enhancements and improvements.

  • Acts as the link between customers and Medable's product development team.

  • Collaborate with product team to scope additional product features and product roadmap.
  • Uses in-depth knowledge of Medable's products to provide technical guidance and support to internal teams. This includes creating and reviewing technical design documentation to ensure development is being built and tested according to technical standards.
  • Supports technical training and onboarding to customers to ensure successful product launches and adoption.
  • Other duties as assigned.
2. Experience
  • 4 + years of technical experience in technical implementation, product management, solution design or a related role, or a combination of education and experience.
  • Ability to understand and interpret clinical trial documentation such as protocols, clinical data models and other eClinical data collection instruments.
  • Demonstrated experience in interpretation of client requirements and solution design to prepare and document design specifications.
  • Experience in requirement gathering, analysis, solution design, development, testing and implementation of software.

  • Strong knowledge of clinical trial data management processes and regulatory compliance frameworks.

  • Comprehensive understanding of clinical trial domains, specifically:
    • eCOA (electronic Clinical Outcome Assessments)
    • ePRO
    • EDC
    • DCT
  • Proven experience in client relations and interactions with clients at all levels.
3. Skills
  • Microsoft Word, PowerPoint, Excel.
  • Excellent verbal and written communication skills, negotiation skills and the ability to translate complex technical concepts into simple terms.
  • Strong technical understanding of SDLC.

  • Exceptional customer-facing and technical communication skills.

  • Proven ability to gather and articulate technical customer requirements.

  • Excellent technical project management and problem-solving abilities.

  • Proficiency in app publication process.

  • Git, Confluence, Postman, Terminal (command line).

  • Strong project management skills.

  • Technical aptitude and ability to learn software programs.

  • Good time-management skills.

4. Education, Certifications, Licenses
  • Bachelor's degree in Computer Science, Health informatics or a related field.
5. Travel Requirements
  • As required.

At Medable, we believe that our team of Medaballers is our greatest asset. That is why we are committed to your personal and professional well-being. Our rewards are more than just benefits - they demonstrate our commitment to providing an inclusive, healthy and rewarding experience for all our team members.

Flexible Work

  • Hybrid from day one – we believe in creating a truly flexible employee experience
     

Compensation

  • Competitive base salary packages

  • Annual performance-based bonuses

  • Employee stock options – aligning your success with Medable's growth
     

Health & Wellness

  • Comprehensive health insurance coverage for you and your family

  • Inclusive parental leave policy for non-birthing parents
     

Recognition

  • Peer-to-peer recognition programs to celebrate achievements and milestones
     

Community Involvement

  • Volunteer time off to support causes that matter to you
     

Medable is committed to providing reasonable accommodations for qualified individuals with disabilities in our job application procedures. If you need assistance or would like to request an accommodation due to a disability, please contact us



  • Bengaluru, Karnataka, India beBeeClinicalData Full time ₹ 12,00,000 - ₹ 20,00,000

    Job Title: Senior Clinical Data SpecialistThe Senior Clinical Data Specialist plays a vital role in ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management. This position involves leading the development of Risk-Based Quality Management (RBQM) plans,...


  • Bengaluru, Karnataka, India beBeeClinicalData Full time ₹ 18,00,000 - ₹ 25,00,000

    Job Title: Data Associate Specialist\This is a critical role in the field of clinical data management. You will work alongside experienced professionals to ensure accurate and compliant data handling for clinical trials.\As a Data Associate Specialist, you will be responsible for verifying clinical data from Case Report Forms (CRFs) into study databases...


  • Bengaluru, Karnataka, India beBeeNursing Full time ₹ 43,20,000 - ₹ 72,00,000

    Job Opportunity: Clinical Nurse SpecialistJob OverviewDevelop and implement comprehensive patient care plans that cater to diverse needs.Collaborate with healthcare teams to ensure seamless delivery of pre- and post-operative care services.Administer medication, intravenous infusions, and other treatments as prescribed by physicians.Conduct thorough...


  • Bengaluru, Karnataka, India Clear Castle Full time ₹ 9,00,000 - ₹ 12,00,000 per year

    The Clinical Support Specialist will be responsible for performing in-center dental assessments, providing consultation for smile correction treatments, and working in coordination with the orthodontics and clinical teams to ensure a seamless customer experience.Key Responsibilities:Educate clients about clear aligner treatments and oral healthExplain...


  • Bengaluru, Karnataka, India beBeeContentSpecialist Full time

    Job Title: Clinical Content SpecialistThis role is a key contributor to the success of our organization, working closely with cross-functional teams to create high-quality clinical content.About the Role:Create, edit, and finalize expert reports based on statistical analysis and scientific conclusions.Develop statistical analysis plans in collaboration with...

  • Quality Assurance

    2 weeks ago


    Bengaluru, Karnataka, India MS Clinical Full time ₹ 1,04,000 - ₹ 1,30,878 per year

    Job Title: Quality Assurance (QA) – Clinical ResearchExperience: 8–10 yearsLocation: Indiranagar, BangaloreDepartment: Quality AssuranceAbout the RoleWe are seeking an experienced QA professional to join MSCR, responsible for ensuring the highest standards of quality and compliance across clinical research operations. The ideal candidate will bring...


  • Bengaluru, Karnataka, India beBeeMedical Full time ₹ 8,00,000 - ₹ 12,00,000

    Clinical Quality Assurance SpecialistThis position plays a vital role in ensuring the accuracy and quality of diagnostic reports.The ideal candidate will have strong analytical and organizational skills to assess report quality, manage time effectively, and maintain accurate documentation.

  • Clinical Expert

    2 weeks ago


    Bengaluru, Karnataka, India beBeeClinical Full time

    Clinical Specialist Job DescriptionJob Overview:We are seeking a highly skilled Clinical Specialist to join our team. This role will be responsible for managing specimen test plans across multiple client instances, planning and establishing timelines to meet business expectations, and allocating time for investigation and resolution implementation.Key...


  • Bengaluru, Karnataka, India Advarra Full time ₹ 6,00,000 - ₹ 18,00,000 per year

    Company InformationAt Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the...

  • Sr Medical Writer

    2 weeks ago


    Bengaluru, Karnataka, India beBeeMedical Full time ₹ 1,50,00,000 - ₹ 2,50,00,000

    Job Title:">Sr Medical Writer - Clinical Document Specialist">">Lead the development and execution of clinical document strategies for trial projects.">Collaborate with cross-functional teams to interpret and analyze data, summarize scientific findings, and communicate insights in written form.">Participate in planning and execution of clinical development...