365 Clinical Operations Jobs - Page 3

We are seeking an experienced and dynamic Sr. Manager / AGM / Head - Operations to oversee and lead the operations of our hospital. The ideal candidate will have a minimum of 15 years experience in hospital operations, with a proven track record in senior roles managing inpatient (IP), outpatient (OP), and emergency services as a team leader. Candidates should have experience working in hospitals with at least 150 beds. Key Responsibilities: Lead and manage day-to-day hospital operations, ensuring smooth functioning across IP, OP, and emergency departments. Develop and implement operational policies, procedures, and standards to enhance patient care and efficiency. Coordinate with clinical, administrative, and support teams to ensure high-quality service delivery. Manage resources, including staffing, budgeting, and equipment allocation, within the approved budget. Monitor and evaluate performance metrics to drive continuous improvement. Ensure compliance with healthcare regulations, accreditation standards, and safety protocols. Foster a collaborative work environment, promoting teamwork and professional development. Prepare reports and present operational updates to senior management. Qualifications & Experience: Master’s in Hospital Administration (MHA) or Bachelor in Hospital Management (BHM). Minimum 15 years’ experience in hospital operations with progressive leadership roles. Experience managing hospitals with 150+ beds is mandatory. Strong leadership, communication, and organizational skills. Proven ability to lead multidisciplinary teams in a fast-paced healthcare environment.

Job Description- Job Title : Executive - Operations Location : Baner, Pune Qualification: Any Graduate Experience Required: 1-3 Years Working Days: 6 Days a Week (Field + Office Work) Key Skills Required : Strong data interpretation and reporting skills Detail-oriented with excellent organizational abilities Ability to handle escalations and daily operations Good communication and stakeholder management skills Job Description: Cross-Functional Coordination : Work closely with Patient Care Specialists, doctors, and hospitals to manage patient admissions, discharges, and case-related processes. Insurance & Documentation Support : Coordinate with the Insurance Department to ensure accurate and timely submission of patient documents. Supply Chain & Vendor Management : Oversee the procurement and logistics of medical equipment to ensure uninterrupted operations. Issue Resolution & Process Management : Handle operational escalations and support daily operations, while identifying opportunities for process improvements and SOP development. About Hexa Health: At HEXA, we are building a platform that will help users choose the right hospital/surgeon for their surgical procedure. We would like to be synonymous with surgery information and discovery. We are working towards building India's largest hospital network, and we will ensure a hassle-free experience for the patient at the hospital. Website Link: https://www.hexahealth.com/ LinkedIn Link: https://www.linkedin.com/company/hexahealth/ Career Page Link: https://www.hexahealth.com/careers Whatsapp Channel Link: https://whatsapp.com/channel/0029VaLmR8IL7UVQUeKlZQ1O

Interested candidates can drop cv on 9773533017

You will be joining our Clinical Operations team in India, Mumbai as a full-time office-based Experienced Study Start-up Submissions Coordinator. Your role will be crucial in accomplishing tasks and projects that are essential for the success of our company. If you are seeking a rewarding career where you can utilize your expertise and further develop and grow professionally, this opportunity is perfect for you. At Medpace, we foster a culture of expertise and empowerment, allowing our teams to leverage their unique talents and experiences to approach research and problem-solving assertively, thereby supporting our business partners effectively. Our employees embody our values and commitment to serving our clients, working diligently, meeting high expectations, and embracing challenges. In return, they receive engaging projects, opportunities for career advancement, and exposure to our international presence. These are some of the reasons why talented individuals choose to be part of the Medpace team. Your responsibilities will include: - Performing necessary activities within the country to activate investigative sites for clinical trials across all phases. - Preparing, reviewing, and submitting documents to Regulatory Agencies. - Communicating with global study teams and personnel to update them on study progress. - Identifying and mitigating risks related to site activations effectively. - Providing expertise and guidance to global study teams regarding ethics and regulatory submissions. - Reviewing and finalizing essential documents required for site activation. - Serving as the main contact for Ethical and Regulatory submission-related activities. - Engaging directly with investigative sites during the study start-up and activation process. - Ensuring that submissions comply with relevant regulations and guidance documents. - Advising sponsors on changing regulations and compliance requirements. - Tracking submissions and ensuring timely filing of documents. Qualifications required: - Bachelor's degree in a scientific field or equivalent education and experience. - Minimum of 4 years of relevant work experience at a CRO, Pharmaceutical Company, or investigative site. - Strong organizational and communication skills. - Proficiency in Microsoft Office, ICH-GCP guidelines, and regulatory guidelines. - Hands-on experience in preparing, reviewing, and submitting regulatory documentation to Ethics Committees and Regulatory Agencies, including responding to queries. - Proficiency in English language. About Medpace: Medpace is a full-service clinical contract research organization (CRO) offering Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise in various major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. With headquarters in Cincinnati, Ohio, we have a workforce of over 5,000 employees spread across 40+ countries. Why Choose Medpace: At Medpace, we believe in People, Purpose, and Passion. We offer a flexible work environment, competitive compensation and benefits package, structured career paths for professional growth, company-sponsored employee appreciation events, and health and wellness initiatives for employees. Our work has been recognized by Forbes as one of America's Most Successful Midsize Companies and we have received numerous CRO Leadership Awards for expertise, quality, capabilities, reliability, and compatibility from Life Science Leader magazine. What to Expect Next: If your qualifications align with our requirements, a Medpace team member will review your profile and contact you with further details regarding the next steps in the process. Thank you for considering a career with us.,

As a Clinical Research Medical Advisor (CRMA) at Novartis, located in Mumbai, you will play a crucial role in overseeing all clinical and medical aspects related to Development and prioritized Research programs/trials in the country. Your responsibilities will include providing clinical strategic and tactical leadership, ensuring optimal clinical trial implementation, and upholding safety standards and clinical data quality. Your key responsibilities will involve offering clinical development and indication expertise specific to the country/cluster, validating study designs, contributing to scientific/clinical/medical aspects during the start-up phase, providing clinical/medical expertise to the clinical trial operations team and sites, developing clinical/medical trial plans, delivering comprehensive training, and supporting internal stakeholders in clinical trials. To excel in this role, you must possess a scientific degree in MD/M.B.B.S, demonstrate the ability to manage studies from a scientific/medical/clinical perspective, showcase problem-solving skills, exhibit effective leadership and communication abilities, showcase agility in different therapeutic areas, and ideally have 3 years of clinical development experience in the pharmaceutical industry or clinical practice. Moreover, a sound understanding of the overall clinical development process and ICH/GCP principles is essential. Novartis offers a compelling mission to reimagine medicine and improve lives, striving to become the most valued and trusted medicines company globally. By joining Novartis, you will be part of a community of driven individuals working towards ambitious goals. The company is dedicated to fostering diversity, building an inclusive work environment, and creating teams that reflect the patients and communities served. If you are interested in staying connected with Novartis and learning about future career opportunities, you can join the Novartis Network. Additionally, Novartis provides comprehensive benefits and rewards to support your personal and professional growth. If you require accommodation due to a medical condition or disability during the recruitment process, Novartis is committed to working with you to provide reasonable adjustments. Join Novartis in its mission to help individuals and families affected by diseases through innovative science and a supportive community. Together, we can achieve breakthroughs that positively impact patients" lives. If you are ready to contribute to a brighter future, consider joining the Novartis team and be part of a network that values collaboration and inspiration.,

Job Summary: The Officer - Onco Solid Oral will be responsible for supporting clinical development activities related to solid tumor oncology therapies, specifically focusing on oral drug formulations. This role involves coordinating clinical trials, liaising with cross-functional teams, ensuring regulatory compliance, and contributing to project timelines and deliverables. Key Responsibilities: Assist in planning and execution of clinical trials for oral oncology products targeting solid tumors. Coordinate with clinical research organizations (CROs), investigators, and internal teams. Monitor trial progress, ensure adherence to protocols, and manage documentation. Support regulatory submissions and maintain compliance with regulatory guidelines. Collect, analyze, and report clinical data related to oral oncology products. Collaborate with medical, pharmacovigilance, and regulatory teams. Prepare clinical study reports and assist in the preparation of publications and presentations. Ensure timely communication and resolution of issues during trial execution. Support budget management and resource allocation for clinical projects.

The Clinic Manager will be responsible for overseeing the daily operations of the clinic, ensuring smooth patient flow, coordinating staff, managing appointments and records, and supporting business growth. Perks and benefits Sunday Holiday Skill Training Uniform

As a Clinical Ops Specialist at Syneos Health in Beijing/Shanghai, you will play a crucial role in ensuring activities are carried out in alignment with Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. Your responsibilities will include supporting Clinical Monitoring staff in site management activities, acting as a Sponsor representative for assigned studies, and maintaining communication with sites to ensure adherence to protocol requirements and study procedures. You will be responsible for creating and managing Trial Master Files (TMF) and project files, participating in file audits, preparing site manuals and reference tools, and updating clinical tracking information in databases. Additionally, you will track clinical and regulatory documents, manage a shared mailbox, process site requests, and coordinate the ordering, packaging, shipping, and tracking of site supplies and materials. Your role will involve assisting in team meetings, preparing accurate meeting minutes and action items, and handling the receipt, tracking, and disposition of Case Report Forms and Queries. By completing all necessary training, you will maintain awareness of developments in the field of clinical research. To qualify for this position, you should have a High School diploma or equivalent, possess strong communication and interpersonal skills, and be adaptable to new technologies. The role may require minimal travel of up to 25%. Syneos Health is dedicated to fostering a supportive and inclusive work environment where employees are encouraged to be their authentic selves. We believe in continuous development and progression, offering career growth opportunities, technical training, peer recognition, and a total rewards program. We are committed to building a diverse and inclusive company culture that values individual perspectives and experiences. At Syneos Health, you will have the opportunity to work on cutting-edge projects and collaborate with a global team of passionate professionals who are dedicated to making a difference in the lives of patients. Join us in our mission to accelerate the delivery of therapies and bring positive changes to healthcare worldwide. For more information about Syneos Health, visit http://www.syneoshealth.com.,

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Database Management team is committed to developing and maintaining databases for clinical trials, which includes creating Case Report Forms (CRFs) and developing Edit and Validation Checks using programming skills like C# and PL/SQL. They also support data integration from various external sources such as labs and Interactive Response Technology (IRT). The team ensures compliance with regulatory standards and guidelines, maintaining high levels of data quality and security. Additionally, they continuously seek to improve database processes and tools by leveraging the latest technologies and best practices to enhance efficiency and accuracyDevelop clinical study databases by building electronic case report forms and program edit checks as per specifications. Support any updates or changes to the study database (e.g. Protocol amendments) through the change control process. What are we looking for Clinical Database ProgrammingClinical Data ManagementSAS ClinicalAdaptable and flexibleAbility to perform under pressureProblem-solving skillsAbility to establish strong client relationshipAgility for quick learningOracle Procedural Language Extensions to SQL (PLSQL)Structured Query Language (SQL)C, C++, C# Programming SkillsExperience in writing programs using Javascript Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualification BE,BTech

About The Role Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Associate Qualifications: BE/BTech Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Database Management team is committed to developing and maintaining databases for clinical trials, which includes creating Case Report Forms (CRFs) and developing Edit and Validation Checks using programming skills like C# and PL/SQL. They also support data integration from various external sources such as labs and Interactive Response Technology (IRT). The team ensures compliance with regulatory standards and guidelines, maintaining high levels of data quality and security. Additionally, they continuously seek to improve database processes and tools by leveraging the latest technologies and best practices to enhance efficiency and accuracyDevelop clinical study databases by building electronic case report forms and program edit checks as per specifications. Support any updates or changes to the study database (e.g. Protocol amendments) through the change control process. What are we looking for Clinical Database ProgrammingClinical Data ManagementSAS ClinicalAdaptable and flexibleAbility to perform under pressureProblem-solving skillsAbility to establish strong client relationshipAgility for quick learningOracle Procedural Language Extensions to SQL (PLSQL)Structured Query Language (SQL)C, C++, C# Programming SkillsExperience in writing programs using Javascript Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualification BE,BTech

Critical Activities Conduct morning meeting in coordination center in-charge to discuss technical details of patients scheduled on daily basis & allot patients to therapists as per skills & schedules Conduct morning meeting with Sales & CRM teams to identify possible patient care packages to maximize revenue potential Consultations with new patients to take their detailed history & understand medical issue to suggest best possible solutions Initiate & continue follow-up discussion with patients in a friendly & professional manner to generate trust & comfort Ensure all pre-procedure instructions are given to & followed by the patients as perp-work for any medical procedures carried out in clinic Study clinical notes, photos, comments on any previous procedure/ consultations done with repeat patients Execute Consultations / medical procedures as per schedule adhering to all Clinical SOPs, Health & Safety Guidelines and treatment plans Planning of Hair Transplant procedures with patients & supporting them during all the pre-surgery procedures Manage team of Therapists to monitor their day-to-day routines, performance & hygiene within clinic premises Overlooking all the procedure done by therapist as he/she is doing the procedure properly Ensure all post-procedure instructions are given to patient in writing & conduct follow up discussions with patients over calls & follow-up visits to assess the success of the procedures/ medicines Prescribe most suitable medicines to patients according to their diagnostics & ensure availability of all necessary medicines in pharmacy Build rapport with patient throughout their journey with Dermatrix to ensure maximum client satisfaction which can lead to positive feedback, testimonials & referrals for the clinic Prepare & store patient notes in proper format for all new & existing patients after each meeting Perform a morning & evening checks of the clinic to ensure that clinic is in hygienic conditions & all tools, instruments, machines, documents & fixtures are in proper order Conduct end-of-day checks before closure of clinic to ensure all tools, instruments, machines, documents & fixtures required next day are working properly & are stored in designated places in proper & hygienic manner Record, Store & Share Before-After Success stories in proper manner (documents, photos, testimonials etc) to build-up patient portfolio Coordinate with Client Relations Team for scheduling & follow-up for patient appointments Regularly upgrade oneself via study of updates/ developments in medical field to provide best possible medical care to our clients Requirement Details Educational Qualification: MBBS / MBBS + MD / MBBS + DVD / BAMS/ BHMS/ BDS (plus course in Cosmetology + Trichology) Work Experience No. of Years Minimum 3 Years post qualification Functional Skills/ Experience Checklist Experience in Conducting procedures in Hair & Skin Treatments Experience in handling Laser Skin Care machines Knowledge of current medicines in Hair & Skin Treatments Strong Diagnosis skills Experience in Patient Handling Behavioral/ HR Fitment Checklist Growth Oriented & Flexible attitude to work Humble & Service Oriented Communication People Management Skills Caring & Solution Oriented KRAs & Performance Scorecard Outputs Expected KRAs Measurement Index Weightage Ensure smooth execution of all clinical procedures by self & therapists via 100% adherence to pre-procedure / during-procedure / Post-procedure SOPs Maintaining High Standards of Medical Care Errors During Medical Procedures 30% Contribute to overall medical & growth targets of the center by handling all clinical / patient care responsibilities Revenue Achieved through Medical Processes Revenue Achieved through Medical Processes 25% Medical assessment of patients to understand their health issues & come up with best possible treatment Convince patients to adopt medical treatment identified after examination & get them enrolled in Clinic Promote the Hair Transplant Services of Dermatrix in ethical & productive manner Ensure Smooth & Productive Inter-Department Coordination Cross-Selling Revenue 10% Coordinate with Sales & CRM teams to ensure smooth doubt solving for clients Monitor & improve performance of the therapist team Ensure 100% adherence to clinical documentation requirements in software tools + hardcopies Complete Adherence to Company SOPs in all work Areas Number of Non-Compliances Seen During the Month 20% Ensure 100% adherence to internal daily/ weekly/ monthly MIS reporting for self & therapist team Establish & maintain coordinal relationship with patients to make them welcomed & comforted in clinic Ensure Complete Client Satisfaction Client Feedback Scores 10% Client Testimonials 5%

Roles and Responsibilities Manage patient care services, ensuring high-quality treatment and satisfaction. Oversee hospital operations, including clinical administration, staff management, and resource allocation. Develop and implement strategies to improve patient relations, counseling, and overall hospital performance. Collaborate with medical teams to ensure seamless coordination of patient care services. Ensure compliance with regulatory requirements and maintain accreditation standards. Desired Candidate Profile MBA/PGDM degree from a reputed institution (preferably in Healthcare or Hospital Administration). Minimum 12-18 years of experience in hospital administration or management consulting industry. Strong understanding of healthcare regulations, policies, and best practices. Excellent communication skills for effective collaboration with cross-functional teams. Please share your resume at kumar.kaustav@medanta.org with subject line (Deputy GM Patient Services) or WhatsApp your resume @9905959704.

Greetings, We are inviting applications for the post of Service Line Manager with a renowned hospital located in Hyderabad Gachibowli Post : Service Line Manager Experience : 5 to 8 Years (from a hospital background) Qualification : MBA or relevant Remunerations : Best as per industry standards For further details, please connect with me at +919220647539 Best Regards,

As a Senior Clinical Operations Specialist (Senior CTA) in the Hybrid model in Athens at Syneos Health, you will play a crucial role in ensuring compliance with Corporate and Clinical Operations Policies, Standard Operating Procedures, and Work Instructions. Your responsibilities will include assisting Clinical Monitoring staff with site management activities, maintaining project files, handling project correspondence, participating in file audits, and preparing and maintaining site manuals and reference tools. Additionally, you will be responsible for updating clinical tracking information into databases, tracking documents, managing the shared mailbox, and coordinating site supplies and materials. You will collaborate with sites on assigned studies, communicate with them to ensure compliance with protocol requirements and relevant guidelines, and serve as a Sponsor representative. Your role will also involve anticipating, identifying, and resolving potential issues, implementing corrective actions, and seeking guidance as needed for more complex matters. Furthermore, you will participate in team meetings, prepare accurate meeting minutes and action items, and maintain awareness of clinical research by completing all necessary training. To excel in this role, you should preferably have an Associate's degree or equivalent experience in clinical research, pharma, biotech, or a related field. Good knowledge of medical terminology, clinical data, and ICH/GCP is preferred. You should possess strong organizational skills, attention to detail, and the ability to prioritize and work on multiple tasks. Excellent communication, presentation, and interpersonal skills are essential, along with the willingness to embrace new technologies. Minimal travel of up to 10% may be required as part of your responsibilities. At Syneos Health, we are committed to developing our employees through career progression, supportive line management, training programs, peer recognition, and a total rewards program. Our Total Self culture encourages authenticity and fosters a sense of belonging among our diverse workforce. By joining us, you will become part of a team dedicated to accelerating the delivery of therapies and changing lives. Syneos Health has a strong track record, having worked on a significant number of FDA-approved drugs, EMA authorized products, and numerous studies across various sites and trial patients. In our dynamic and competitive environment, you will be empowered to challenge the status quo and drive innovation. If you are passionate about making a difference in the field of clinical research and are looking for a challenging yet rewarding opportunity, consider joining Syneos Health. Learn more about us at http://www.syneoshealth.com.,

QuartzBio is the Precision Medicine Intelligence Company, focused on utilizing the Precision Medicine AI Agent Platform to enable autonomous data ingestion and conversational insights across the precision medicine value chain. The platform, powered by a network of domain-specific AI agents, aims to amplify the efforts of operations, translational, informatics, and IT teams by integrating biomarker, sample, and clinical data to create a unified, scalable data ecosystem. This accelerates the time from data to insights, analytics, and visualizations, ultimately transforming the way precision medicine teams work with 360 intelligence. As a Business Analyst Manager (Business Intelligence) at QuartzBio, you will play a crucial role in guiding strategic decision-making through advanced business intelligence, data analysis, and cross-functional collaboration. The ideal candidate for this role should possess deep analytical expertise, hands-on data analysis skills, a strong understanding of Business intelligence technologies, and the ability to convert ideas into product requirements. You will be responsible for leading complex analytics initiatives, analyzing stakeholder business intelligence requirements, and enabling the Product Development Life Cycle (PDLC) process within the analytics workstream. Key Responsibilities: Product Strategy & Feature Management: - Manage the intake and prioritization of business intelligence product requests. - Decompose product requirements into features and translate them into detailed epics and user stories. - Collaborate with product leads to define release scopes and develop product roadmaps. - Define and manage business and technical requirements for core BI components and data pipeline initiatives. Technical Analysis & Integration: - Conduct backend data pipeline analysis to enrich and validate feature requests. - Translate complex or ambiguous problems into structured analyses and communicate insights to both technical and non-technical stakeholders. - Work closely with AI and intelligent agent teams to integrate BI capabilities with virtual assistants and intelligent systems. Cross-Functional Collaboration: - Lead product grooming sessions with stakeholders to align on product deliverables. - Collaborate with the design team to create user journey maps, wireframes, and other UX deliverables. - Partner with engineering teams during sprint demos to review progress and provide product feedback. - Define and implement QA processes in collaboration with the QA team to ensure high product quality. Adoption, Enablement & Innovation: - Drive adoption of business intelligence and semantic layers to empower business users with self-service analytics. - Own the full project lifecycle, from scoping and stakeholder alignment to delivery, documentation, and user enablement. - Identify opportunities to leverage generative AI to automate insights, enhance reporting, and improve user experience. Continuous Improvement: - Stay current with BI and analytics trends, tools, and best practices in SaaS environments. - Continuously enhance technical skills and remain informed about emerging technologies in the BI space. Qualifications: - Bachelor's degree in a related field and a minimum of 8 years of relevant work experience in Business and technical analysis tasks related to Business intelligence. - Advanced proficiency in SQL/MySQL, data visualization tools (e.g., Tableau, Power BI, Looker), and data modeling concepts. - Experience with modern data stacks and familiarity with GenAI tools and frameworks is a plus. - Strong project management skills and experience in clinical operations and Biomarker data analytics are preferred. - Excellent communication skills, analytical skills, and problem-solving abilities. Leadership Expectations: - Follow the company's principles and code of ethics. - Appreciate individual talents, differences, and abilities of team members. - Support change initiatives and continuous process improvements. - Communicate effectively with colleagues, supervisors, and clients. Please note that any data provided as part of the application process will be stored in accordance with our Privacy Policy. If you require a reasonable accommodation to complete the application process or need an alternative method for applying, please contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com.,

Job Title : Perfusionist No. of Vacancies : 1 Salary : As per company norms Job Type : Technical Reports To : Director Biomedical Division Job Location: Vadodara Bachelor's degree in Perfusion Technology or a related field. Minimum 3–5 years of hands-on experience in a clinical setting. Experience or interest in R&D, medical devices, or product testing is preferred. Familiarity with regulatory standards such as ISO 13485, CE, or FDA is advantageous. Strong analytical, problem-solving, and communication skills. Key Skills: Proficiency in providing clinical demonstrations of perfusion systems and engaging with hospital clinical teams. Ability to articulate the benefits of perfusion products to potential customers, fostering long-term relationships. Strong ability to translate clinical needs into engineering requirements. Comfortable working in cross-functional teams (engineering, QA, regulatory, etc.). Knowledge of CAD, prototyping, and basic data analysis tools is a plus. Willingness to travel occasionally for clinical trials or customer feedback. Business Development Acumen: Ability to identify market opportunities, develop strategies to increase market share, and actively engage with clients and stakeholders to drive sales growth. Job Responsibilities: Collaborate with biomedical engineers and product designers in developing cardiac surgical devices and perfusion systems. Provide clinical insights on the design, usability, and functionality of heart-lung machines, oxygenators, blood pumps, and related equipment. Participate in simulation testing and validation of new devices. Assist in creating clinical trial protocols and supporting documentation. Conduct product evaluations in both simulated and real clinical settings. Stay updated with the latest clinical perfusion techniques, equipment standards, and safety guidelines. Support regulatory and quality assurance teams with technical insights. Educate internal teams on perfusion procedures and equipment usage. Prepare reports, presentations, and product improvement recommendations. Participate in training programs and conduct demonstrations for new products. Business Development Role: Drive growth in the perfusion product line by identifying new business opportunities, nurturing client relationships, and contributing to marketing and sales strategies. Develop and implement strategies for market expansion and customer retention. Apply here : https://forms.gle/zbrsHksfczvPSyu26 Contact details : hr@medinnovasystems.com | 6358944452 For more details : Visit career page at www.medinnovasystems.com

Job Title: AGM / DGM – Clinical Trials (Protocol & Report Writing) Department: Clinical Research / Clinical Operations Minimum 10–15 yrs of relevant experience in clinical trials, protocol writing, CSR writing, and regulatory documentation

• Implement and configure clinical trial solutions as per client requirements. • Collaborate with clients and internal teams for smooth project execution. • Provide training, documentation, and post-implementation support Required Candidate profile • 4+ years of IT solution implementation experience in Healthcare/Clinical Trials/Life Sciences. • Hands-on experience with CTMS, LIMS, EDC, or similar systems preferred. Perks and benefits - GPA &term Insurance-5 days week -Flexible timing

- Collaborate with project managers to define scope, timelines, and deliverables - Ensure timely and effective execution of clinical trial software solution projects - Provide consulting for CTMS platform implementation, configuration Required Candidate profile - Advise on solution architecture, workflows, and usability enhancements in CTM systems - Validate the alignment of software features with clinical workflows and regulatory requirements Perks and benefits -GPA &term Insurance -5 days week -open to discuss

Project Role: Centralized Monitoring Lead Work Experience: 4 plus years of CRA and Clinical trials and monitoring. Work location: Bangalore/Thane/Pune/Ahmedabad/Kochi/Hyderabad Work Mode: Hybrid/Office Based Shift: 2.00pm to 11.00pm Must Have Skills: Onsite / Remote / Risk Based Monitoring, Clinical Research, Clinical trials. Job Responsibility: Oversight of clinical deliverables across all trial phases (start-up to close-out). Development and review of study management plans, risk assessments, and analytics strategies. • Monitoring of site performance, key risk indicators (KRIs), and operational triggers. Financial oversight including budget tracking and investigator payments. Coordination of cross-functional teams to meet project milestones. Quality assurance through regular audits, documentation, and compliance checks. Leading data review processes and ensuring audit readiness at all times. May require taking up Clinical lead activities, Manage Finance related information (budget, CO etc.), Manage project resources (CRAs/CTAs/Centralized monitoring team), Conduct periodic review of site activities Technical Skills: Requires minimum of 5 years of relevant experience or Medical degree with a minimum 4 years of clinical trial experience or equivalent combination of education, training and experience. Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements. i.e., International Conference on Harmonisation - Good Clinical Practice (ICH GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct. Good Clinical system expertise

As the Oncology Senior Director Disease Area Lead at GSK, you will play a pivotal role in driving the global strategy for clinical operations within your assigned portfolio. You will ensure operational excellence, accelerate development timelines, and optimize delivery to support GSK's mission of improving health outcomes worldwide. In this role, you will lead a high-performing global team of Clinical Operations Asset Leads and Associate COALs, setting the strategic vision and operational direction for delivering the disease area portfolio including Early Phase strategy and delivery for the Disease Area. You will contribute to the Business Development strategic input by providing leadership, conducting due diligence, and building a clinical development plan in preparation for governance. Additionally, you will lead the Disease Area Matrix Leadership Team by partnering with key stakeholders to shape the vision and resourcing/delivery strategy to support the clinical portfolio from design through regulatory submission/approvals. Your responsibilities will include providing leadership and coaching to team members, fostering a culture of innovation, accountability, and high performance. Collaboration with the GCO TA head to set the strategic direction for the GCO TA teams, ensuring alignment with GSK's R&D objectives and overall company strategy is a key aspect of this role. You will be accountable for all operational aspects of the Disease Area, providing strategic oversight and ensuring delivery against key milestones, timelines, and quality standards. Moreover, you will identify and integrate best practices across the organization, implement strategies to mitigate risks associated with clinical program delivery, and drive delivery optimization and accelerate development timelines across the life cycle of an asset. Your role will also involve shaping and sustaining a culture of excellence, collaboration, accountability, and innovation within the organization. To qualify for this position, you should hold a Bachelor's degree in a scientific discipline with knowledge and experience in Oncology drug development at a senior strategic level within Clinical Operations. Proven line and matrix leadership skills, exceptional negotiation abilities, and experience in leading organization-wide problem-solving are essential. An advanced degree in a scientific discipline and expertise in driving innovative solutions are preferred qualifications for this role. If you are a visionary leader who thrives in a dynamic, collaborative environment and is passionate about delivering excellence, this Oncology, Senior Director Disease Area Lead role at GSK is an exciting opportunity to shape the future of clinical operations and make a meaningful impact on health outcomes worldwide. Apply now and be part of a team that unites science, technology, and talent to get ahead of disease together.,

Roles & Responsibilities: Core Objective: To handle operations of the center seamlessly Drives the center revenue and achieves target Contributes directly to top line revenue Core Skills: Good oral and written communication skills in Regional Language, English Good people skills, be a Team player - Networking & Relationship Building Personal integrity, ability to deal with sensitive issues with tact, diplomacy and judgment Maintain complete discretion and confidentiality Planning, Organizing, Prioritizing & Time Management skills Personal Grooming, Good Etiquette Ability to handle stress, crisis management & extended working hours. Job description Ensure smooth functioning of all healthcare operations in the assigned hospital. Responsible for day to day operations of the branch focusing on customer service, quality, people management and process adherence. Handling the revenue of the hospital. Ensure smooth functioning of the assigned branch. Tracking branch performance. Focus on patient satisfaction and quality. Credit billing status to be monitored. Pending ALs to submission of bills. Checking of Counsellors reports daily for Advise Vs Converted / Counselled. Conducting Weekly and Monthly reviews with Counselors, Floor managers and PCA. Report to be submitted to Management. Giving On Job training to Counselors, Patient care associates. Random Counseling. Random Patient Calls (Post OP Patients, General Patients, Emergency Cases) Interaction with Doctors about Targets, High Value Cases & Procedures. Co-ordination with Surgeons. Attending to patient Complaints of your zone & speaking to them personally. Prepare monthly tour plan and submit for approval. Daily and monthly report with summary of area with explanation. Define and drive Standard Operating Procedures for service excellence.

Skill required: Clinical Data Services - Clinical eTMF Management Designation: Clinical Data Svs Associate Qualifications: BTech/Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects. Strategies, methods and tools used throughout the lifecycle of the clinical trial regulated content. Includes data review and accuracy checks of trial master file table of contents, head quarters, initial full protocol package and amended FPP checklists, end of trial checklists, essential document reconciliation, and clinical study report appendices. What are we looking for? Adaptable and flexible Problem-solving skills Detail orientation Ability to establish strong client relationship Agility for quick learning Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualification BTech,Bachelor of Pharmacy,Master of Pharmacy

Role & responsibilities Participate in the investigator recruitment process. Perform initial qualification visits of potential investigators and sites. Evaluate the capability of the site to successfully manage and conduct the clinical study, both clinically and technically. Work with the Study Start-up Group to coordinate activities with the site in preparation for the initiation of studies. Obtain regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Perform study initiation activities, reviewing with the site study team the protocol, regulatory issues, study procedures, and provide training on completion of the e-CRF; monitoring activities and study close-out activities. Train site study team on the EDC system. Conduct periodic site file audits to ensure compliance with GCPs and sponsors standard operating procedures. Assure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Perform validation of source documentation as required by sponsor. Prepare monitoring reports and letters in a timely manner as per Clinical Trial Monitoring Plan. Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture Document accountability, stability and storage conditions of clinical trial materials as required by sponsor. Perform investigational product inventory. Ensure return of unused materials to designated location. Review the quality and integrity of the clinical data through in house review of electronic CRF data and on-site source verification. Work with sites to resolve data queries. Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Coordination with central and corelab (Echocardiography, QCA, OCT/IVUS, ECG) involved in the clinical trial. Review protocols, eCRFs, ICF and other related documents, as requested by Project Manager. Assist with final date review and query resolution through database lock. Online & offline regulatory/IEC submissions of different countries. Coordination with DSMB, Steering committee, CEC and attend meetings and prepare minutes of meetings. Preparation of study presentation for review meetings at Central Drug Standard Control Organization Regulatory Body of India. Preparation of Study presentation for national & international conferences.

Job Summary The IPDRG Medical Coder is responsible for assigning accurate codes to inpatient medical records, ensuring compliance with coding standards and contributing to the efficiency of healthcare processes. Key Responsibilities Assign IPDRG codes to inpatient medical records based on established guidelines and regulations. Review and interpret clinical documentation to ensure accurate coding. Collaborate with healthcare professionals to resolve documentation discrepancies. Meet coding accuracy and productivity targets. Stay informed about updates to coding standards and practices. Required Qualifications Certification: Valid CPC (Certified Professional Coder), CCS (Certified Coding Specialist), or CIC (Certified Inpatient Coder) certification required. Experience: Minimum of 1 year of experience in IPDRG coding. Education: Background in healthcare, medical coding, or a related field preferred. Skills: Proficiency in IPDRG coding systems and guidelines. High attention to detail and accuracy. Analytical and problem-solving skills. Strong communication and teamwork abilities. Mandatory Key Skills clinical documentation,healthcare coding,coding compliance,medical coding,IPDRG Medical Coder,IPDRG coding.