
Clinical Trials Specialist
5 days ago
A seasoned Business Analyst role in the Healthcare and Life Sciences domain, focusing on Clinical Trials and Clinical Operations.
- Lead requirements gathering sessions with stakeholders across Clinical Operations and IT teams.
- Author and maintain User Requirement Specifications (URS) and ensure alignment with business and regulatory needs.
- Support User Acceptance Testing (UAT) by preparing test scripts, coordinating execution, and capturing feedback.
- Manage Jira boards for tracking user stories, tasks, bugs, and deployment workflows.
- Act as a domain consultant and business analyst across multiple technology implementations within the clinical trials value chain.
- Collaborate with cross-functional teams including developers, testers, product owners, and business users in an Agile environment.
Domain Expertise:
- Medidata Rave
- Clinical Trial Management Systems (CTMS)
- Randomization and Trial Supply Management (RTSM)
- Contract Research Organizations (CROs)
- Planisware (for clinical planning and portfolio management)
- 5-8 years of experience as a Business Analyst in the Life Sciences / Pharmaceutical industry.
- Strong domain knowledge in Clinical Trials and Clinical Operations processes.
- Proven experience in Agile software development and delivery.
- Hands-on experience with clinical trial systems and tools mentioned above.
- Excellent communication, documentation, and stakeholder engagement skills.
- Experience in managing end-to-end software development lifecycle from requirements to deployment.
-
Clinical Trials Consultant
1 week ago
Mysore, Karnataka, India beBeeBusiness Full time ₹ 17,99,277 - ₹ 23,89,159Job OverviewWe are seeking an experienced Business Analyst to lead clinical trial implementations and provide business consulting services within the Life Sciences industry.This role requires a strong domain consultant with expertise in Clinical Trials and Clinical Operations processes, as well as proven experience in Agile software development and...
-
Clinical Trial Statistician
6 days ago
Mysore, Karnataka, India beBeeBiostatistics Full time ₹ 1,50,00,000 - ₹ 2,50,00,000Senior Biostatistics LeaderThe biostatistics leader is responsible for developing and implementing statistical strategies and deliverables in support of clinical trials. This role contributes to the planning, execution, and interpretation of statistical analyses across development programs.Main Responsibilities:Lead biostatistical efforts for assigned...
-
Senior Clinical Trials Business Consultant
4 days ago
Mysore, Karnataka, India beBeeBusiness Full time ₹ 60,00,000 - ₹ 1,50,00,000Job Title: Life Sciences Business ExpertAbout the Role:We are seeking a seasoned Business Analyst with 5-8 years of experience in the Healthcare and Life Sciences domain, focusing on Clinical Trials and Clinical Operations. The ideal candidate will have hands-on experience with clinical trial systems and a strong track record of delivering technology...
-
Senior Clinical Trial Manager
4 days ago
Mysore, Karnataka, India beBeeClinicalOperationsLead Full time ₹ 17,81,600 - ₹ 24,86,400Job DescriptionWe are seeking a skilled Clinical Operations Lead to oversee the success of our global clinical trials. In this role, you will be responsible for leading a team of clinical professionals and ensuring that all projects meet their recruitment targets.The ideal candidate will have a strong understanding of the clinical research industry and...
-
Mysore, Karnataka, India beBeeStatistical Full time ₹ 20,00,000 - ₹ 25,00,000Senior Statistical Programmer Role Overview">Advanced Clinical is a clinical development and strategic resourcing organization dedicated to delivering exceptional clinical experiences throughout the drug development process.The company approaches each opportunity with foresight, character, resilience, and innovation, helping clients achieve better outcomes...
-
Independent Healthcare Professional
1 week ago
Mysore, Karnataka, India beBeeTelugu Full time ₹ 25,00,000 - ₹ 50,00,000Freelance Clinical Trial InterviewerWe are seeking a skilled healthcare professional to conduct clinical trial screening interviews in India.As a freelancer, you will work on key tasks including:Contacting candidates within 48 hours of their volunteering on our platformConducting interviews based on a provided scriptReceiving paid training on specific...
-
Clinical Quality Assurance Lead
2 days ago
Mysore, Karnataka, India beBeequality Full time ₹ 10,26,000 - ₹ 12,74,000Job OverviewWe are seeking an experienced Quality Assurance Specialist to provide day-to-day clinical quality assurance support across ongoing clinical trials.This individual will play a key role in guiding study teams, maintaining compliance with Good Clinical Practice (GCP), and ensuring quality oversight.Key Responsibilities:Serve as the primary QA...
-
Clinical Research Professional
4 days ago
Mysore, Karnataka, India beBeeResearch Full time ₹ 7,00,000 - ₹ 15,00,000Job Title: Clinical Research ProfessionalAre you passionate about clinical research and eager to grow in a structured, accredited environment?As a Clinical Research Associate at Clinogenesis Research Organization, you will have the opportunity to launch your career in clinical research.The role involves assisting with on-site coordination of clinical trial...
-
Senior Clinical Data Analyst
7 hours ago
Mysore, Karnataka, India beBeeDataAnalyst Full time ₹ 20,00,000 - ₹ 25,00,000Job Description:Sponsor-Dedicated Statistical Programmer Role. Collaborate with pharmaceutical clients to drive patient treatment innovation, leveraging advanced SAS programming skills and CDISC standards expertise.The role involves working as part of a global team to support Phase I-IV clinical trials, applying scientific rigor to data analysis and...
-
Regulatory Compliant Document Specialist
4 days ago
Mysore, Karnataka, India beBeeClinicalResearch Full time ₹ 15,00,000 - ₹ 25,00,000Clinical Study SpecialistTransforming complex scientific data into regulatory compliant documents is a key responsibility in this role. Documents such as protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs) require high-quality development to drive drug development and...