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0.0 - 1.0 years
3 - 6 Lacs
Hyderabad
Work from Office
Job Summary : As a Clinical reporting analyst you will be integral to our mission of providing accurate and timely analysis of ECG data, contributing to the improvement of patient care and outcomes. looks forward to your contributions to our team and the impact you will make in enhancing our data processing capabilities. Join us in embracing the startup vibe of agility, open communication, and teamwork. Here, you'll thrive in an environment where learning, challenging the status quo, and unleashing your creativity are encouraged. Your voice matters, and together, we move swiftly, learn from missteps, and make meaningful impacts. Let's forge ahead, innovate, and make a difference. Come be a part of our dynamic team! Job Responsibilities: Every candidate goes through a 6 week training program. The training covers ECG Analysis training, data processing techniques and software training. Once the training completes, your primary duties will include: Sanitise and process up Beat data as per the standard process. Prepare up Beat data with appropriate highlights for further processing. Effectively communicating ECG abnormalities by notifying lead technicians and/or physicians and clinical staff as necessary. Maintaining compliance with job-specific proficiency requirement. Your specific responsibilities may change from time to time at the discretion of t Company. You will also be expected to comply with all rules, policies, and procedures of the Company, as they may be adopted and modified from time to time. Candidate Requirements: 12th grade + Diploma in cardiology or Bachelors Degree in Zoology, lifesciences. Experience as a Holter Scanner or telemetry / monitor technician will be an added advantage . Proficiency level in handling computers. Excellent attention to detail . Positive attitude and team player, ability to use critical thinking skills . Knowledge of medical terminology, specific to Cardiology and Electrophysiology. Excellent written and verbal communication skills . Strong analytical, communication, and interpersonal skills.
Posted 5 days ago
4.0 - 9.0 years
8 - 16 Lacs
Pune, Bengaluru, Mumbai (All Areas)
Work from Office
Greetings from You & I Consulting! We've proudly helped candidates build careers at 64+ top MNCs across India, and were excited to bring you a new opportunity with a leading global company. If you have experience in Statistical Programming , this role is your next step forward! To Apply: Send your CV via WhatsApp or Call : Puja- (8250242229) or email your resume at :- puja@careersuni.com Shift - General Shift Open Locations :- Mumbai Pune Bangalore Hyderabad Indore Ahmedabad Key Responsibilities: Lead and oversee statistical programming activities for clinical trials at compound/indication/TA level Design and develop SDTM and ADaM datasets as per CDISC standards Generate Tables, Listings, and Figures (TFLs) for clinical study reports and regulatory submissions Manage and review deliverables for eSubmissions, including Define.xml and reviewer guides Provide technical leadership and mentorship to global programming teams Collaborate closely with biostatistics, data management, and regulatory affairs teams Support and lead Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) projects Ensure programming compliance with SOPs, FDA/EMA guidelines, and quality standards Required Qualifications: Bachelors or Masters degree in Statistics, Computer Science, or a related field 10+ years of SAS programming experience in clinical research or pharmaceutical industry Strong hands-on experience with ADaM, TFLs, eSubmissions, and integrated analysis Deep understanding of CDISC standards, regulatory compliance, and submission requirements Prior experience in oncology, neuroscience, or immunology domains preferred Proven leadership capabilities in managing cross-functional and global teams Excellent communication, project management, and problem-solving skills Preferred Tools & Skills: SAS (Base, Macro, STAT, Graph) Familiarity with SDTM/ADaM IG, FDA submission standards Understanding of regulatory submission formats (eCTD) How to Apply / Schedule an Interview: Send your details via WhatsApp or Call : Puja- (8250242229) in the following format: Full Name: Mobile Number: Email Address: Highest Qualification: Total Experience: Current Organization: Preferred Location: Current CTC: Expected CTC: Notice Period: Note: If the line is busy, please drop a WhatsApp message and we will get back to you at the earliest. Referrals Welcome! Know someone who fits the bill? Share this post and help them grow their career! You & I Consulting Your Career Growth Partner
Posted 1 week ago
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