5 Clinical Reporting Jobs

As an Implementation Consultant, you will be responsible for managing and assuming accountability for all aspects of projects related to implementation. Your key responsibilities will include guiding the client through release planning, managing communication throughout the team and stakeholders, leading product implementation efforts, coordinating with customers, product SME, and other teams, managing the quality of implementation deliverables, and documenting and reporting status on Risks, Issues, Actions, and Decisions. You will need to identify, report, and manage risks while overcoming project obstacles. Acting as a client liaison and representative, you will communicate client feedback to appropriate representatives and act to resolve outstanding issues on behalf of the client in a timely manner. Understanding the client's clinical landscape, you will provide techno-functional solutions to evolving client needs. Your role will involve analyzing and understanding current business processes, events, and flows in Clinical Trial Development. You will create SOPs and Work instructions for the implementation/delivery team to ensure a smooth transition of services from implementation to support. Additionally, you should be able to incorporate feedback and input from customers, partners, and in-house teams on product features. Desired Skills: - Experience in the Lifesciences and Pharmaceutical industry is essential - Good experience in SQL, APIs, and Integrations - Good understanding of CDASH, SDTM, and ADAM standards - Good understanding of EDC Systems, CTMS Systems, IRT Systems, and LAB Systems - Knowledge of clinical trial domain, EDC study setup, and clinical reporting - Ability to build clinical reports and dashboards - Relevant degrees such as Bachelor's and Master's Degree in Healthcare, Computer Science, Technical, Engineering, Computer, Computer Engineering, Computer Programming - 3-5 years of experience as a Product Manager or 1-2 years of experience as a Product Owner - Comfortable and familiar with the Agile Working Environment - Experience working with all phases of SDLC - Familiarity with FDA regulations such as 21 CFR Part 11 and GxP is a bonus - Experience working in the complete product life cycle of two or more products - Technical knowledge including Software Development and Web Development - Experience with the use and configuration of healthcare software applications (preferably clinical),

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.

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.

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

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.