Merck KGaA

Clinical Trial Feasibility Specialist

Posted On

Oct. 24, 2024

Location

Bangalore, Karnataka

Experience Level

C - Professional (1-3 years)

Job Type

Full-time

Apply By

Dec. 24, 2024

Job Description

Job Listing: Clinical Trial Feasibility Specialist Location: Bangalore, India Bringing new medications to patients in need is what drives us to bring our best selves to work every day. The Clinical Trial Feasibility Specialist will be part of the innovative and diverse Operational Design Center (ODC) supporting study and Global Product Teams. Reporting to the Head, Operational Design Center, the Feasibility Specialist will conduct data mining of internal and external databases for use in the development of robust operational strategies for global clinical trials. Your research and analysis will include disease background, current and projected future standards of care, competitive landscape, enrollment benchmarking and enrollment modeling. You will use site databases and local cross-functional input for study-level operational planning and potential site identification. You will support consistency of deliverables and development of best practices within and beyond the ODC. You will join a strong and diverse team with variety of professional and personal backgrounds that collaborates transparently and with a focus on delivering for impact. We are known for our innovation efforts, continuously looking for ways to be more efficient and effective. The work of the ODC informs key decisions made by study teams and senior leaders. If you have a minimum of 3 years working in a CRO, vendor, or sponsor Feasibility Team, this could be the perfect job for you. Who you are:Bachelors degree in scientific or business area3+ years of clinical trial feasibility experience supporting data-driven decision makingFamiliarity with relevant operational and feasibility data, applications, and systems used in the pharmaceutical industryExcellent analytical and problem-solving skills Solid organizational skills, high quality focus and result orientationAdvanced Excel and Powerpoint skills Proactively addresses and manages risks and issue escalationAbility to work on multiple projects simultaneouslyExperience working with diverse cross-functional and international teamsExceptional interpersonal skills, including ability to communicate clearly and actively contribute to team meetingsFluency in English ResponsibilitiesResearch scientific/clinical information that may include but is not limited to: disease background, current standards of care, how the proposed intervention fits into the current and projected future treatment landscape, and competing therapeutics in clinical development.Conduct data mining of internal and external databases for use in development of robust operational strategies for global clinical trials (country/site mix, site identification, enrollment scenario modeling.)Use site intelligence and local cross-functional input for study-level operational planning and potential site list identificationSupport consistency of deliverables and development of best practices Identify, analyze, and describe the competing clinical trial landscape to assist in assessing trial feasibilityMaintain detailed records of work and create and maintain internal libraries and databasesCollate results of various analyses into a comprehensive, yet concise report, with tables, graphs and all cited references.Participate in intra and inter-departmental meetings Support development and evolution of ODC data and analytic capabilities to advance clinical trial operational planning and data-driven decision making We are an equal opportunity employer that values workforce diversity. We want everyone to be able to bring their best self to work every day which is why equality and inclusion is at the forefront of all our activities. We are dedicated to a policy of non-discrimination in employment on any basis including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity.

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