Study Grant Analyst II

4 weeks ago

REMOTE, India Parexel Full time

Build Grant EstimateTimely preparation of accurate and competitive Clinical Study grants (Phases I – IV for all clinical indications) via proficient usage of any Clinical Study Pricing Tool that PAREXEL is required to use to support our Clients' needs. The default, currently licensed tool in this regard is Grant Plan.Collaborate to prepare competitive budget concepts for Pre-sales business Proposals in conjunction with other members of the Proposal team while remaining compliant with the Request for Proposal (RFP) and PAREXEL internal policies.Subject Matter Expert and Lead on the creation, revision, escalation, and approval process of Clinical Study grants for awarded Projects with the assigned Site Contracts Leader and Study Project Leader and Project Director, as appropriate.Preparation of additional Post Award Clinical Study grant analyses for the assigned Site Contracts Leader and Study Project Leader and Project Director, as appropriate.Participation in strategy sessions and budget reviews when requested to develop win themes, identify, and assess competitor's benchmarks and discuss client needs.Ensure that all Clinical Study grant information is performed in full compliance with Fair Market Value (FMV) principles and the Physician Payments Sunshine Act.Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, etc.)Display good knowledge sharing capabilities, share lessons learnt and new scenarios with the team.Deliver and maintain client-focused Grants analysis to measure performance and proactively identify issues for resolutionSupport & build departmental or functional training plans, content & deliveryGeneral Administration & Operations Maintain a working knowledge of, and assure compliance with, applicable ICH Guidelines, Good Clinical Practices, Regulatory Agency requirements, and PAREXEL SOPsParticipate in, Parexel and department system/standards improvement activities or committees, task force groups as needed, including change management.Ensure agreed levels of productivity/billability are maintained Complete routine administrative tasks in a timely manner (e.g. timesheets, training, travel expense claims). Ensure compliance with travel and billability guidelines for department, region, or function, are met where appropriate.Maintain a positive, results orientated work environment, building partnerships, and modeling teamwork, communicating to the team in an open, balanced and objective manner.Ensure implementation of process improvements in response to client and team feedback and quality auditsLook within and beyond GLE to encourage teamwork, quality and productivity efforts to the benefit of GLE and PAREXEL #LI-REMOTE

  • Statistical Programmer-ii

    1 month ago

    Remote, India Parexel Full time

    As a member of Parexel’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and Parexel teams in differing locations. Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and...

  • Medical Writer Ii-narratives

    1 month ago

    Remote, India Syneos Health Clinical Full time

    **Description** **Medical Writer II** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers...

  • QA Tester Ii

    1 month ago

    Remote, India Duck Creek Technologies Full time

    Job Description Helping careers take flight. Reshaping an industry. Enable your career to be Made on Duck Creek. WHO WE ARE: Duck Creek Technologies is the intelligent solutions provider defining the future of the property and casualty (P&C) and general insurance industry. We are the platform upon which modern insurance systems are built, enabling the...

  • Clinical Trial Coordinator Ii

    4 weeks ago

    Remote, India Thermo Fisher Scientific Full time

    Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. - Ensures allocated tasks are performed on time, within budget and to a high quality standard. Escalates in cases of variances...

  • Oncology Site Monitor II

    4 weeks ago

    REMOTE, India Parexel Full time

    Key Accountabilities:Start-up (from site identification through pre-initiation):Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase. Build relationships with investigators and site staff. Conduct, drive and manage country specific feasibility and/or site pre-qualification and...

  • Statistical Programmer 2

    4 weeks ago

    Remote, India IQVIA Full time

    Job Overview Provide advanced technical expertise to develop and maintain programs to meet internal and external clients’ needs. Plan and lead the development of project-related solutions to the full scope of statistical programming tasks. Provide technical expertise to the Statistical Programming department. Essential Functions - Perform and plan: (i)...

  • Data Management Lead II

    1 month ago

    REMOTE, India Parexel Full time

    Data Management Lead llThe Data Management Lead ll provides leadership and expertise in all aspects of Data Management. Develop and manage timelines for study data deliveries, including Go-Live, Interim Deliveries, and Final DB Lock. Collaboration with the relevant functions (Clinical, Biostatistics, Database Programming, Medical, Medical Writing etc.)...

  • Regulatory Project Assistant, India

    4 weeks ago

    Remote, India Innovaderm Research Full time

    The Regulatory Project Assistant (RPA) is responsible for providing project administrative support to the regulatory project team members (regulatory affairs, eTMF operations). The RPA also supports activities within the regulatory website Clinical Trial Information System (CTIS) ensuring completeness and timely entry of information for EU submissions. The...

  • Site Intelligence Analyst I

    4 weeks ago

    REMOTE, India Parexel Full time

    Support Feasibility site and country selection in create project site list and survey questionnaire in system based on CFL's requirements.Investigator and Center data quality improvement.Programming skills such as SQL, Python is a plus to create tool to provide efficient work solution.Advanced computer skills including MS-Office products such as Word, Excel,...

  • Data Scientist

    1 month ago

    Remote, India Plaxonic Full time

    **Job Title - Data Scientist** **Location - REMOTE** **Job Type - Contract** **Contract Length - 3-6 Months** **Shift - Night Shift** **Responsibilities**: - Perform a thorough study of the data provided by the dataset - Pose insightful business queries in plain language that the data can handle - Write effective, high-quality Snowpark Python code to solve...

  • Principal Safety

    6 days ago

    Remote, India Syneos Health Clinical Full time

    **Description** **Principal Safety & Pharmacovigilance Specialist** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide...