Clinical Trials Specialist

5 days ago

Kochi Kerala, India Feathersoft Full time

Job Summary We are seeking a highly experienced Clinical Trials Specialist with a background in pharmaceuticals or a Contract Research Organization CRO to join our product development team This is a unique opportunity to step out of the traditional clinical operations role and apply your deep domain expertise to shape the next generation of clinical trial software You will serve as the subject matter expert ensuring our AI platforms are built on a solid foundation of real-world clinical research principles and address the most pressing challenges in trial design and execution Key Responsibilities Subject Matter Expertise Act as the primary internal consultant on all aspects of clinical trial design planning and protocol development Product Development Collaboration Work closely with software engineers data scientists and product managers to translate complex clinical trial concepts into functional software requirements and AI model features Protocol Design Input Provide expert review and guidance on trial protocols study designs e g adaptive trials decentralized trials basket trials and endpoint selection to inform the logic to automate the workflows of our platforms Feature Validation Test and validate new software features and AI-driven recommendations to ensure they are clinically sound compliant and user-friendly for research professionals Content Algorithm Curation Assist in curating extracting and structuring clinical data from scientific literature and regulatory guidelines to train and refine our AI models Market User Insights Stay abreast of industry trends regulatory changes e g ICH CDSCO and the evolving needs of clinical research professionals to guide product strategy Requirements Required Qualifications Experience Educational Background A degree in Life Sciences Pharmacy Medicine or a related field is required An advanced degree Masters PhD PharmD is highly preferred Industry Experience A minimum of 7-10 years of hands-on experience working within a pharmaceutical company or a CRO Core Expertise Proven significant experience in the design and development of clinical trial protocols across different therapeutic areas and phases Phase I-IV Must have prepared and submitted clinical trial-enabling documents Regulatory Knowledge Deep understanding of the end-to-end clinical trial process Good Clinical Practice GCP and international local regulatory guidelines e g ICH-GCP FDA EMA CDSCO Analytical Mindset Strong analytical skills with the ability to deconstruct complex clinical processes into logical steps Desired Skills Passion for technology and innovation in the life sciences sector Familiarity with the software development lifecycle or experience working with technology teams is a huge plus Exposure to or a keen interest in learning Artificial Intelligence Machine Learning and data analytics Excellent communication and interpersonal skills with the ability to articulate complex scientific concepts to a non-scientific audience A proactive problem-solving mindset and the ability to thrive in a fast-paced collaborative startup environment

  • Clinical Trial Psych Rater

    1 week ago

    India, Cochin / Kochi / Ernakulam IQVIA Full time

    Job Description Clinical Specialist Consultant - Gukarati Speaking Location: Remote/virtual Hours: Estimated 10-16h/month Role: Clinical Specialist Job Description: The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality...

  • ▷ (Apply Now) Clinical Trial Psych Rater - Punjabi Speaking

    2 weeks ago

    India, Cochin / Kochi / Ernakulam IQVIA Full time

    Job Description Clinical Specialist Consultant - Punjabi Speaking Location: Remote/virtual Hours: Estimated 10-16h/month Role: Clinical Specialist Job Description: The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of...

  • Clinical Research Associate

    6 days ago

    Ahmedabad, Kochi, Kolkata, India Airvin Skills Full time ₹ 2,00,000 - ₹ 6,00,000 per year

    Job Type- Fresher or Internship levelClinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe.Responsibilities:Assist in Protocol Development:Collaborate with the...

  • Clinical Data Specialist

    4 weeks ago

    Kochi, India IQVIA Full time

    Role: Clinical Data specialist Skill: CDM, Rave Mode: Hybrid Experience: 2-5 years in Clinical Data management Job Location: Kochi/Kolkata/Bangalore Educational Qualification: Any life science graduate Job Overview: Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data...

  • Clinical Data Specialist

    4 weeks ago

    Kochi, India IQVIA Full time

    Role: Clinical Data specialist Skill: CDM, Rave Mode: Hybrid Experience: 2-5 years in Clinical Data management Job Location: Kochi/Kolkata/Bangalore Educational Qualification: Any life science graduate Job Overview: Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data...

  • Clinical Db Designer

    1 week ago

    Kochi, Kerala, India IQVIA Full time

    Job Overview Responsible for study design, edit specifications and system configurations. The Clinical database designer is accountable for associated quality and timely delivery of assigned study design components in collaboration with other project stakeholders. Essential Functions - Interprets the study protocol. - Design and update the eCRF. - Create...

  • Clinical Data Coder 1

    4 hours ago

    Kochi, Kerala, India IQVIA Full time

    and quality data management products) to Data Management (DM) team to meet sponsor and company needs. Perform Clinical Data Management and/or Coding activities, and may provide leadership either in the role of the Lead Coder or in a specific CDM task (e.g. Data Operations Coordinator (DOC) or lead a coding related task on a mega trial). Essential...

  • Assoc Clinical Specialist

    3 days ago

    Kochi, India Medtronic Full time

    At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Responsibilities may include the following and other duties may be assigned. Conducts on-site...

  • Clinical Data Specialist

    4 weeks ago

    Kochi, India IQVIA Full time

    Role: Clinical Data specialistSkill: CDM, RaveMode: HybridExperience: 2-5 years in Clinical Data managementJob Location: Kochi/Kolkata/BangaloreEducational Qualification: Any life science graduateJob Overview:Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management...

  • Clinical Data Specialist

    1 week ago

    Kochi, India IQVIA Full time

    Role: Clinical Data specialistSkill: CDM, RaveMode: HybridExperience: 2-5 years in Clinical Data managementJob Location: Kochi/Kolkata/BangaloreEducational Qualification: Any life science graduateJob Overview:Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management...