1328 Ophthalmology Jobs - Page 15

NHS Greater Glasgow and Clyde is one of the largest healthcare systems in the UK employing around 40,000 staff in a wide range of clinical and non-clinical professions and job roles. We deliver acute hospital, primary, community and mental health care services to a population of over 1.15 million and a wider population of 2.2 million when our regional and national services are included. The shift pattern for this post is Monday to Friday 9am to 5pm. We are seeking an enthusiastic, dynamic and innovative individual to support nursing leadership at a senior level across GG&C Ophthalmology services. Ophthalmology is a citywide service spanning 7 sites and currently sits under the South Sector. In this challenging role, you will inspire others and lead by example, fostering a culture of continuous quality improvement which values professional development and strives for excellence in all aspects of the delivery of patient care. The post holder will collaborate with the senior management team ensuring the achievement of activity, financial, and staff performance targets, as well as maintaining quality standards. Budget and staff management, along with business planning, are integral to this role. As a registered nurse with a first degree, or equivalent experience, you should possess management expertise gained in the NHS or a similarly complex multidisciplinary public or private sector organisation. We are value strong influencing and leadership qualities along with a proven track record of successful delivery and collaborative work. If you believe your skills align with our requirements, we encourage you to submit your application. Informal enquiries and visits are welcomed. Please contact Liza Campbell, Clinical Services Manager on 0141 232 2215 or email liza.campbell2@ggc.scot.nhs.uk Details on how to contact the Recruitment Service can be found within the Candidate Information Packs NHS Greater Glasgow and Clyde encourages applications from all sections of the community. We promote a culture of inclusion across the organisation and are proud of the diverse workforce we have. By signing the Armed Forces Covenant, NHSGGC has pledged its commitment to being a Forces Friendly Employer. We support applications from across the Armed Forces Community, recognising military skills, experience and qualifications during the recruitment and selection process. Candidates should provide original and authentic responses to all questions within the application form. The use of artificial intelligence (AI), automated tools, or other third-party assistance to generate, draft, or significantly modify responses is strongly discouraged. By submitting your application, you confirm that all answers are your own work, reflect your personal knowledge, skills and experience, and have not been solely produced or altered by AI or similar technologies. Failure to comply with this requirement may result in your application being withdrawn from the application process. For application portal/log-in issues, please contact Jobtrain support hub in the first instance.

Req Ophthalmologist 10yr phaco, sics cataract surgery please send CV at armjob2025@gmail.com Ph 9415408154 9648661122 9919720600

Job Summary: We are seeking an experienced and confident Staff Nurse to lead our nursing team. The successful candidate will be responsible for overseeing nursing staff, ensuring high-quality patient care, and maintaining adherence to OR protocols. The ideal candidate will possess strong leadership skills, a bold and authoritative demeanor, and the ability to motivate and guide the nursing team. Key Responsibilities: 1. Leadership: - Lead and supervise a team of nurses, providing guidance and support as needed. - Foster a positive and productive work environment, promoting teamwork and collaboration. - Make decisions and take actions to ensure efficient workflow and high-quality patient care. 2. Patient Care: - Provide direct patient care, utilizing strong clinical skills and knowledge. - Assess patient needs, develop care plans, and implement interventions. - Evaluate patient outcomes and make adjustments to care plans as needed. 3. OR Protocols: - Ensure adherence to OR protocols, policies, and procedures. - Stay up-to-date on current best practices and guidelines. - Collaborate with other departments to maintain a safe and efficient OR environment. 4. Communication: - Communicate effectively with patients, families, and healthcare team members. - Document patient information accurately and efficiently. - Participate in multidisciplinary team meetings and contribute to decision-making. 5. Professional Development: - Stay current with nursing trends, best practices, and evidence-based research. - Participate in ongoing education and training, maintaining professional certifications as required. Requirements:- Education: BSc Nursing or equivalent - Experience: Minimum 1-3 years of experience in a similar setting, with experience in OR nursing preferred Background Required-Opthalmology - Skills: - Strong leadership and communication skills - Ability to work in a fast-paced environment - Knowledge of OR protocols and procedures - Ability to prioritize tasks and manage time effectively - Strong critical thinking and problem-solving skills - Certifications:Current nursing registration and relevant certificationsIf you're a motivated and confident nurse leader with a passion for delivering high-quality patient care, we'd love to hear from you.

Leads project-specific certification activities at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Performs certification data entry and works in the certification database at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Assists with providing support in tracking, compiling, and submitting project deadlines and deliverables Assists with the collection of electronic and paper-based project files and archives Assists with the review of study related documents, certifications and data to ensure quality and accuracy Supports the coordinating of conference calls and meetings Edits, formats, tracks and distributes technical and non-technical reports Attends and participates in department team meetings Performs other duties as assigned Overview Ophthalmic Certification Project Associate India - Bangalore Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients lives and act accordingly. We stive to build a collaborative culture at the intersection of being a performance and people driven company. We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! This requirement is for our OptymEdge division. OptymEdge sets the gold standard for training and certification in ophthalmic clinical trials and brings experience and expertise from having the largest and longest-standing certification organization in the industry. Pioneering visual acuity certification from conception, we have developed proven solutions for training and certification of Visual Function Examiners and Visual Function Rooms, and partner with study teams to provide visual function certification that ensures a high level of quality and consistency for ophthalmic clinical trial data. OptymEdge has certified over 2000 sites worldwide since 1995, working on Phase I through post-marketing trials in clinical Ophthalmology, Optometry, and other therapeutic areas. Primary Purpose The Ophthalmic Certification Project Associate (OCPA) is critical to the successful conduct of ophthalmic certifications in Biopharmaceutical-sponsored clinical trials. The OCPA supports the Manager, Ophthalmic Certification Project Management Group (OCMPG) and Ophthalmic Certification Project Managers by providing logistical support for electronic document filing and archiving, reporting requirements and other duties required by the statement of work. The OCPA will be site-facing through the life cycle of the study, and contributes to team and financial efficiency, work product quality, and client satisfaction through strong relationship management. Responsibilities Leads project-specific certification activities at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Performs certification data entry and works in the certification database at the direction of the Manager, OCMPG and Ophthalmic Certification Project Managers Assists with providing support in tracking, compiling, and submitting project deadlines and deliverables Assists with the collection of electronic and paper-based project files and archives Assists with the review of study related documents, certifications and data to ensure quality and accuracy Supports the coordinating of conference calls and meetings Edits, formats, tracks and distributes technical and non-technical reports Attends and participates in department team meetings Performs other duties as assigned Qualifications Bachelor s degree preferred or equivalent experience will be considered 2 years demonstrating related experience Demonstrated experience with MS Office Suite, particularly MS Word Time management and decision-making skills Attention to detail and the ability to address several assignments simultaneously Excellent oral and written communication skills Some knowledge of clinical trials in ophthalmology preferred CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

Dear Sir/Madam, We are urgently looking for Doctors for various Medical Colleges and Hospitals across India. For Medical Colleges, we require the following in all Clinical & Non-Clinical Departments: * Senior Residents * Assistant professors * Associate Professors * Professors * Medical Superintendents * Dean/Principals For Hospitals: Consultants & Surgeons in All Clinical Departments *** Please reply at the earliest to avail the most suitable position *** WEPS is the Topmost Healthcare Recruitment Firm in India. We recruit healthcare professionals for a variety of the Medical Colleges & Hospitals in the country. For further information and to upload your resume, please visit Regards, Tanu Goyal WEPS SCO 12, LGF, Hollywood Plaza, VIP Road, Zirakpur, SAS Nagar, Punjab 140 603 Email: weps.careers@gmail.com Mob: 7015609544 whatsapp@87015609544

Responsibilities: * Maintain confidentiality at all times * Collaborate with ophthalmologists on patient treatment plans * Provide eye education and guidance * Assess patient needs and concerns

Urgent Hiring: Ophthalmologist (Multiple Locations) | Immediate Joining | High Salary Company: Doctors Recruiter (Powered by Tech India) Job Type: Full-Time / Consultant / Part-Time Experience: 020 Years Salary: Best in Industry | Negotiable | Incentives Available Open Positions in the Following Locations: Siddharth Nagar (Uttar Pradesh) Kashipur (Uttarakhand) Katni (Madhya Pradesh) Sangli (Maharashtra) Bareilly (Uttar Pradesh) Sahibganj (Jharkhand) Ramgarh (Jharkhand) AAYODHYA(UP) BASTI(UP) Key Responsibilities: Conduct routine eye examinations and diagnose vision problems Perform cataract, glaucoma, LASIK, and other surgeries (as per specialization) Prescribe corrective lenses or treatment plans Collaborate with optometrists, nurses, and surgical teams Maintain accurate medical records and ensure follow-up care What We Offer: Competitive salary + performance-based incentives Accommodation (at select locations) State-of-the-art hospital equipment Supportive work environment Immediate joining preferred Freshers & experienced professionals welcome Educational Qualification: MBBS + MS/DOMS/DNB in Ophthalmology Valid MCI/State Medical Council registration Ophthalmologist jobs in Uttar Pradesh Eye specialist doctor vacancy MS Ophthalmology job openings Ophthalmologist jobs with immediate joining DOMS doctor jobs India Eye hospital hiring Ophthalmologist MBBS MS Eye doctor jobs Doctor jobs in Sangli, Kashipur, Bareilly, Katni, Ramgarh, Sahibganj Ophthalmology consultant jobs India Ophthalmologist hospital jobs 2025 Apply Now Limited Vacancies Available! Doctors Recruiter Talent Acquisition Team www.doctorsrecruiter.com WhatsApp/Mobile: 9808351411/749996000 Email: [Your Email Address] #OphthalmologistJobs #EyeSpecialistJobs #DoctorJobsIndia #HospitalHiring #MSOphthalmologyJobs #DOMSJobs #EyeSurgeonVacancy #ImmediateJoiningDoctors #DoctorsRecruiter #SangliJobs #BareillyJobs #KatniJobs #KashipurDoctors #SiddharthNagarDoctorVacancy #JharkhandDoctorHiring

We are seeking to appoint an enthusiastic and forward-thinking Peri-operative staff nurse to work within the Ophthalmology Theatre at the National Treatment Centre - Highland (NTC). Ophthalmology experience is preferential, but training could be provided if required. The NTC-H is a new purpose-built centre which provides care for both Ophthalmology and Orthopaedic Patients. The Centre is located at the City's University Campus and has 5 theatres, a 24-bedded ward and dedicated Ophthalmology Outpatient Department. The Ophthalmology Theatre comprises of 3 theatres specialising in cataract, glaucoma, oculoplastic and vitreoretinal surgery. Orthopaedic day case hand and foot procedures are also performed two days per week. The role would involve scrub within the peri-operative environment for patients having Ophthalmology surgery. The Ophthalmology Theatre is a fast-paced environment with a high turnover of patients. We are looking for a nurse to complement the existing team. Visits to the department are welcome.

Roles & Responsibilities: Checking of refractive power by Auto Refractometer. Checking the intraocular pressure by Tonometer. Taking Patient History. Checking Subjective Refraction and Retinoscopy. Checking color blindness. Checking EOM (Extra Ocular Movements and Pupil Reaction) Contact Lens fitting and dispensing. Cataract Investigation: A - Scan, B - Scan, IOL Master, Keratometry, Syringing and Specular Microscopy. Glaucoma Investigation: Autoperimetry, OCT Handing over the case sheets to next department. * Responsibilities can be modified subject to necessity. Interested candidates can reach out on 9566082242 or email on anusha.t@dragarwal.com

Alcon Laboratories (India) Pvt. Ltd is looking for Territory Sales Executive DEOH to join our dynamic team and embark on a rewarding career journey Developing and executing a sales plan to achieve revenue and profitability targets in the assigned territory Building and maintaining relationships with key customers and decision-makers, including conducting regular business reviews and identifying opportunities for additional sales Identifying new business opportunities in the assigned territory through market research, competitive analysis, and prospecting Conducting product presentations and demonstrations to prospective customers and facilitating the sales process Providing support and training to customers to ensure effective use of products and services Collaborating with other departments such as marketing, product development, and customer service to ensure customer needs are met Should have excellent communication and interpersonal skills, a strong customer focus

A premier education institution in North India, affiliated with Baba Farid University of Health Sciences and recognized by the NMC, offers a variety of medical programs. It's 1625-bedded, NABH accredited hospital prioritizes patient care, compassion and quality. We invite applications for the following positions:- Associate / Assistant Professor in Biochemistry Assistant Professor in Microbiology, ENT and Emergency Medicine Senior Residents in Ophthalmology, Biochemistry, Emergency Medicine and Microbiology Non-PG Residents (Eligibility MBBS) Eligibility as per NMC Norms. For Further Information kindly contact: 82889-69200 Mail your CV to principal@dmch.edu by July 15, 2025.

Key Responsibilities 1. Conduct comprehensive eye examinations at patients homes, including refraction, screening for common eye conditions. 2. Handle portable diagnostic equipment responsibly and maintain its cleanliness and calibration. Travel allowance

Position Title: CQA Document Control Associate Department: Clinical Quality Assurance Ora Values the Daily Practice of … Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor At Ora, we are building the future of ophthalmic clinical research. As the world's leading full-service ophthalmic drug and device development firm, we guide our clients across all phases of clinical research to efficiently bring new products and therapies to market. Over the past 45 years, our expert teams have helped earn more than 85 new product approvals. Ora's pre-clinical and clinical models, unique methodologies, integrated clinical data solutions, and global regulatory strategies have been refined and proven across thousands of global projects. Today, our team continues to expand across the globe, with over 600 employees across North America, Europe, Asia, and Latin America. The Role: Our global Clinical Quality Assurance (CQA) Document Control Associate will support our Quality Management team to ensure accuracy and efficiency throughout every aspect of the Quality Document Control system. This position provides support to the CQA Document Control Specialist and is responsible for maintaining electronic training files and tracking compliance across the company, in accordance with guidelines and regulations. This position requires a strong organizational background to assist in maintaining Ora's EMS and providing companywide support for training tracking, assignment, and reporting. In this role, you will be trained on preparing, updating/revising, and maintaining all Quality Management System Documents (procedures, policies, work instructions, forms, templates, and manuals) in addition to maintaining tracking reports to present metrics for Key Performance Indicators to report to Ora's Senior Management team. What You'll Do: Ensure, with supervision, proper maintenance of clinical documentation databases and systems Assist with running reports and tracking status of Quality Assurance metrics Assist with change management for Quality document revisions Assist with editing documents needed for the QMS Upload, assign, and track training within Ora's Electronic Management System (EMS) Review external distribution requests, obtain approvals, and distribute documents utilizing Ora's approved document sharing platform Assist CQA Document Control Specialist with managing EMS user accounts, training records, system access issues, uploading QMS and study-specific documents Maintain adequate records of all Quality and operational documents Travel requirements less than 10% domestically Adhere to all aspects of Ora's quality system. Adhere to all essential systems and processes that are required at Ora to maintain compliance to Ora's data integrity & business ethics and regulatory requirements. Clear and sustained demonstration of Ora's values - prioritizing kindness, operational excellence, cultivating joy and scientific rigor – as well as their linked behaviors. Responsibilities may differ from the above based on the specific needs of the business. What We Look For: Experience needed for the Role: Bachelor's degree in Life Sciences or a minimum of 1 year experience in Quality-related field. Years of experience may be considered in lieu of education. Experience working with document management/training software applications Additional Skills and Attributes: Familiarity with the clinical trial process and clinical Quality Assurance Experience in other areas of GCP/GLP/GMP Quality Assurance Competency in Microsoft Office Word, Excel, and Outlook applications Ability to work well in a team environment and follow procedures Strong commitment to the accomplishment of tasks Ability to work in a fast-paced environment Exceptional attention to detail with emphasis on accuracy and quality Excellent verbal and written communication skills Excellent organization and time management skills Strong interpersonal and customer service skills Competencies and Personal Traits: What We Do: Execution Excellence: Ability to set goals, create structure and maintain a focused and collaborative approach to the delivery of timely and high-quality work. How We Do It: IQ, EQ and SQ: Agile and positive thinker, communicator and collaborator who uses a growth mindset to work and lead with authenticity, transparency, resilience, and empathy. Scientific, intellectual, and emotional/social curiosity creates the willingness and ability to innovate, make mistakes, learn and try again. Clear and Direct Communication, Feedback and Conflict Resolution: Practice radical candor in your communication and participate in active Giving and receiving feedback frequently, with an open heart and mind creates psychological safety and promotes faster, individual, team and company growth. Why We Do It: Seek Meaning and Purpose and a Desire to be Part of Something Bigger than Yourself: Crave being part of a team that works together under shared values to achieve significant positive impact in the wider world. At Ora, we are creating vision beyond what we see. Our mission is to weave together people, processes, and technology to support innovation in ophthalmology around the world. We believe our business should be a force for good — to improve, heal, and change how we see. As a global company, our vibrant community and culture are nurtured by our core values: Prioritizing kindness, cultivating joy, operational excellence, and scientific rigor. Through our commitment to these values, we have built an inclusive and supportive work environment that fosters respect, accountability, and a fulfilling work-life balance for every team member. We know a diverse workforce adds to our collective value and strength as an organization. People of color, the LGBTQIA+ community, disabled candidates and veterans are strongly encouraged to apply. Ora is proud to be an Affirmative Action and Equal Opportunity Employer, committed to equal employment opportunity and fair, equitable compensation regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Our Privacy Policy | Ora (oraclinical.com)

We are looking for a Passionate Ophthalmologists to join our team in various specialties: Squint and Pediatric Ophthalmology Specialist, Cataract Surgeon, Anterior Segment Specialist (proficient in Phaco - Emulsification Cataract Surgery Consultant Ophthalmologist – Across all Subspecialties, Fellowship trained The candidate should be able to handle OPD and perform surgical procedures of their specialties' independently. Remuneration commensurate with experience

*Pediatrician / Neonatologist Vacancies* Bathinda Punjab DM Neonatologist Required Salary Rs 5 Lakhs Ludhiana Punjab NNF Fellowship Course Stipend 2 to 2.5 Lakhs + Accommodation Panipat Haryana DM Neonatologist Required Salary 5 Lakhs + Required Candidate profile Hodal Haryana Salary 3 Lakhs + Accommodation Roorkee Uttarakhand DM Neonatologist Req. Salary 6 Lakhs + Accommodation Gadchiroli Maharashtra Salary 3 to 3.5 Lakhs + Accommodation + Food

Position Title: CQA Document Control Associate Department: Clinical Quality Assurance Ora Values the Daily Practice of … Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor At Ora, we are building the future of ophthalmic clinical research. As the world’s leading full-service ophthalmic drug and device development firm, we guide our clients across all phases of clinical research to efficiently bring new products and therapies to market. Over the past 45 years, our expert teams have helped earn more than 85 new product approvals. Ora's pre-clinical and clinical models, unique methodologies, integrated clinical data solutions, and global regulatory strategies have been refined and proven across thousands of global projects. Today, our team continues to expand across the globe, with over 600 employees across North America, Europe, Asia, and Latin America. The Role: Our global Clinical Quality Assurance (CQA) Document Control Associate will support our Quality Management team to ensure accuracy and efficiency throughout every aspect of the Quality Document Control system. This position provides support to the CQA Document Control Specialist and is responsible for maintaining electronic training files and tracking compliance across the company, in accordance with guidelines and regulations. This position requires a strong organizational background to assist in maintaining Ora’s EMS and providing companywide support for training tracking, assignment, and reporting. In this role, you will be trained on preparing, updating/revising, and maintaining all Quality Management System Documents (procedures, policies, work instructions, forms, templates, and manuals) in addition to maintaining tracking reports to present metrics for Key Performance Indicators to report to Ora’s Senior Management team. What You’ll Do: Ensure, with supervision, proper maintenance of clinical documentation databases and systems Assist with running reports and tracking status of Quality Assurance metrics Assist with change management for Quality document revisions Assist with editing documents needed for the QMS Upload, assign, and track training within Ora’s Electronic Management System (EMS) Review external distribution requests, obtain approvals, and distribute documents utilizing Ora’s approved document sharing platform Assist CQA Document Control Specialist with managing EMS user accounts, training records, system access issues, uploading QMS and study-specific documents Maintain adequate records of all Quality and operational documents Travel requirements less than 10% domestically Adhere to all aspects of Ora’s quality system. Adhere to all essential systems and processes that are required at Ora to maintain compliance to Ora’s data integrity & business ethics and regulatory requirements. Clear and sustained demonstration of Ora’s values -- prioritizing kindness, operational excellence, cultivating joy and scientific rigor – as well as their linked behaviors. Responsibilities may differ from the above based on the specific needs of the business. What We Look For: Experience needed for the Role: Bachelor’s degree in Life Sciences or a minimum of 1 year experience in Quality-related field. Years of experience may be considered in lieu of education. Experience working with document management/training software applications Additional Skills and Attributes: Familiarity with the clinical trial process and clinical Quality Assurance Experience in other areas of GCP/GLP/GMP Quality Assurance Competency in Microsoft Office Word, Excel, and Outlook applications Ability to work well in a team environment and follow procedures Strong commitment to the accomplishment of tasks Ability to work in a fast-paced environment Exceptional attention to detail with emphasis on accuracy and quality Excellent verbal and written communication skills Excellent organization and time management skills Strong interpersonal and customer service skills Competencies and Personal Traits: What We Do: Execution Excellence: Ability to set goals, create structure and maintain a focused and collaborative approach to the delivery of timely and high-quality work. How We Do It: IQ, EQ and SQ: Agile and positive thinker, communicator and collaborator who uses a growth mindset to work and lead with authenticity, transparency, resilience, and empathy. Scientific, intellectual, and emotional/social curiosity creates the willingness and ability to innovate, make mistakes, learn and try again. Clear and Direct Communication, Feedback and Conflict Resolution: Practice radical candor in your communication and participate in active Giving and receiving feedback frequently, with an open heart and mind creates psychological safety and promotes faster, individual, team and company growth. Why We Do It: Seek Meaning and Purpose and a Desire to be Part of Something Bigger than Yourself: Crave being part of a team that works together under shared values to achieve significant positive impact in the wider world. At Ora, we are creating vision beyond what we see. Our mission is to weave together people, processes, and technology to support innovation in ophthalmology around the world. We believe our business should be a force for good — to improve, heal, and change how we see. As a global company, our vibrant community and culture are nurtured by our core values: Prioritizing kindness, cultivating joy, operational excellence, and scientific rigor. Through our commitment to these values, we have built an inclusive and supportive work environment that fosters respect, accountability, and a fulfilling work-life balance for every team member. We know a diverse workforce adds to our collective value and strength as an organization. People of color, the LGBTQIA+ community, disabled candidates and veterans are strongly encouraged to apply. Ora is proud to be an Affirmative Action and Equal Opportunity Employer, committed to equal employment opportunity and fair, equitable compensation regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Our Privacy Policy | Ora (oraclinical.com)

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Project / Program Management No Regular Full-Time 2555 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Sr Project Specialist India Bengaluru/hybrid Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Senior Project Specialist provides support to Emmes Global Project Management teams, determining workflows, providing logistics support for conference calls, meetings, supplies, documentation, problem solving, and client/sponsor reporting needs and interactions as required by the statement of work or other corporate/client/sponsor requirements. This position provides oversight to Project Specialists and Clinical Project Coordinators. This role supports BioPharma portfolio projects Responsibilities Supports Global Project Manager (GPM) responsibilities to ensure the contracted services are in accordance with the executed contract and Client/Study expectations. Acts as a secondary point of contact in with study vendor(s). Supports vendor management to ensure effective oversight of third-party vendors. Contributes to project milestone tracking and schedule management. \ Supports GPM in project resource requests and study FTE allocation and tracking. Supports GPM in risk management activities. Schedules and attends internal and external team meetings. Leads and/or assists GPM in internal team meetings and portions of external team meetings as applicable. Supports agenda preparation and prepares and distributes meeting minutes for internal and external meetings. \ Assists GPM in Facilitating communication between staff and client regarding project development and project processes. Extracts information from designated clinical trial management system (CTMS) and other systems/tools to track/analyze study progress for the GPM (e.g., regulatory documents, enrollment, SAE/AEs, protocol deviations, supplies, ethics approvals, data queries) along with coordinating and drafting status reports for internal and external stakeholders. Supports project administrative activities for internal and external audits. Oversees TMF activities to ensure the TMF is maintained in inspection ready state. Tasks include but are not limited to: tracking of quality and status of document filing, timeliness of document filing, collaborate with TMF group to ensure contemporaneous TMF maintenance. Assists the GPM with project financial management activities including monthly projections and budget tracking. Develops study documents and plans, using project-specific knowledge. Establishes and maintains procedures and processes (e.g., SOPs, work practices) in conjunction with departments and broader Company. May also contribute to corporate SOP development. Performs periodic review of allocated project specific internal business records and associated project TMF as needed. Serves as administrator of shared workspace and Emmes Systems for assigned projects. Assists with onboarding, offboarding, and training records for project staff. Manages document retention and archive of project. Provides oversight of Project Specialists and Clinical Project Coordinators. Performs other duties as assigned. Qualifications Bachelor’s Degree or equivalent qualification. Minimum 6 years of relevant project or administrative support experience. Required Skills/Abilities Strong familiarity and working knowledge of Microsoft Office applications, particularly MS Word, Excel, SharePoint, Teams and Emmes systems. Strong analytical skills. Must be able to organize and manage workload efficiently and prioritize projects with minimal supervision. Must be able to work with minimal supervision to perform work that is varied and should be able to work to tight timelines. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

JOB_DESCRIPTION.SHARE.HTML CAROUSEL_PARAGRAPH JOB_DESCRIPTION.SHARE.HTML India - Bengaluru Project / Program Management No Regular Full-Time 2588 Emmes Global mail_outline Get future jobs matching this search or Overview Job Description Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience. We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us! Primary Purpose The Senior Project Manager, Initiatives is responsible for the project life cycle for various organizational initiatives, some of which are listed in the Emmes Strategic Scorecard. This position works closely with members of the Executive and Operations Team, who serve as Executive Sponsors of initiatives. This position is expected to hold information confidential and act as a trusted confidant of Executives. The Senior Project Manager, Initiatives will manage all aspects of assigned initiatives of varying complexity and medium to large size by assembling work groups, assigning individual responsibilities, identifying needed resources, developing schedules to ensure timely project completion, identifying critical capabilities, project resources, budgets, risks and critical path issues. As the senior member of the team, this position provides training, coaching and mentoring to junior team members, and manages direct reports Responsibilities Manages overall initiative lifecycle, including the day-to-day activities of planning, coordinating, implementing, monitoring, documenting, and completing assigned initiatives across global teams. Monitors initiatives to ensure initiative framework processes are being followed and project management best practices are being used, including reporting on metrics related to initiative health, completion of milestones on time and within budget, and adoption of effective change management processes. Coordinates tasks and communication within and across teams and develops presentation materials for projects and executives. Partners with business leaders to ensure alignment of initiative scope and deliverables with business and corporate strategies. Facilitates or leads initiative meetings to develop efficient and effective future state outcome and to identify deliverables needed to ensure initiative goals are met. Works with Business Analyst Manager to develop an effective change management plan for assigned initiatives, then serves as the change agent champion and lead the execution of the change management plan. Compiles and provides monthly initiative status reports, KPIs and metrics related to health of assigned initiatives to executive sponsors, stakeholders, and peers, including key updates, cost, schedule, status, and risks. Exercises independent discretion and judgment to solve complex problems regarding project, department, or division-related work. Promotes, develops, and maintains disciplined initiative project management models and frameworks (and related tools and processes) across Emmes and its subsidiaries; ensures adherence, adoption, implementation, and review of lessons learned. Initiates and shares learning opportunities for the initiative team to continue to grow as professionals. Coordinates activities with Business Analyst and/or Application Analyst assigned to initiative. Assists with tracking project expenditure. Provides training, coaching, and mentoring to junior team members. Provides management to direct reports and leadership to full team. Manages vendor relationships during vendor-run implementations. Performs other duties as assigned. Qualifications Undergraduate degree in business or humanities field preferred. 10+ years of project/program/portfolio management experience with demonstrated increase in responsibility and project complexity, including managing enterprise level business and technology transformation projects as well as resource management, financial management, and/or budget analysis. PMP or equivalent certification and a proven track record of successfully managing projects in a fast-paced business. Experience building customer and stakeholder relationships with a focus on problem resolution. Experience explaining technical terms to non-technical staff. Exceptional project management skills with ability to multitask and manage multiple projects across diverse global teams in a highly matrixed environment. Demonstrated planning and project management skills. Excellent listening, communication, presentation, interpersonal skills, both written and verbal, with an ability to inform, influence, convince and persuade. Strong skills in prioritization, organization, decision-making, time management, and planning. Ability to drive to tangible results in a timely manner even when the work involves a highlevel of ambiguity. Skilled in facilitating meetings with multiple stakeholders, including building consensus, motivation, and managing conflict. Strong analytical, problem-solving, and troubleshooting skills; with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy. Ability to demonstrate strategic thinking capability, exercise good judgement, make sound decisions, and escalate issues/decision making as appropriate. Knowledge of technology concepts including Software Development Life Cycle (SDLC), process improvement, and agile methodologies is preferred. Experience in O365, Smartsheet or MS Project, and Jira is preferred. CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

Alembic Pharmaceuticals is looking for Jr. Executive(Operator) - Manufacturing (Injectable) for our Formulation Unit-3, Karakhadi. Job Criteria: 1-7 years ITI/Diploma qualification Job Responsibility: Perform assembling as per defined procedure. Operate filling machine/ Ophthalmic/ PFS machine. Operate homogenizer. Perform batch filtration activity. Perform aseptic manufacturing activity. To unload steam sterilizer and bio-decontamination chamber in co-ordination with equipment preparation and sterilization area. To take part in area qualification activity. To take part in periodic area requalification activity. Aseptic area equipment qualification, filling machine qualification, media fill process. Interested candidates may share their resumes to " injectable@alembic.co.in "

The Clinical Application Specialist is responsible for providing clinical education and support for Aerogen nebulizer products in hospital accounts within the designated India region. The successful candidate will collaborate with team members, the Commercial Director, and other stakeholders to optimize customer experience, maximize sales, and gain market share. What are the key responsibilities Increase Aerogen nebulizer utilization in Acute Care (Hospital System) to gain market share and support sales targets. Provide clinical user support. Deliver customer training in the hospital setting, empowering customers to use Aerogen nebulizers effectively and independently. Comply with mandatory training and attend local and abroad training programs to maintain knowledge. Collaborate with the Country Manager, Aerogen teams, and distributors to develop innovative activities and achieve sales targets. Maintain relationships with key opinion leaders (KOLs) and important stakeholders. Understand customer needs and objectives to develop tailored solutions that maximize market potential. Stay informed about competitors' products, activities, and strategies in the Indian market. What education and experience are required Degree and/or recognized Clinical Education. Minimum 3-5 years of relevant experience in the medical field. Experience in respiratory therapy, including training and responsibility is preferred What key skills will make you great at the role Fluent in English, both verbal and written communication. Excellent interpersonal skills and the ability to build strong relationships. In-depth product and procedure knowledge to effectively communicate with key stakeholders. Self-disciplined, organized, and takes ownership of business objectives. Highly motivated and driven to succeed. Team player and independent thinker. Ability to positively influence thinking, behavior, and gain commitment. Resident within India with flexibility to travel within India up to 70%. What is it like to work at Aerogen Our purpose is to transform patient lives and our ethos is to #discoverbetter. This also translates to how we look after our people. We want talented, passionate and engaged people to join Aerogen and build your career with us. We understand that your life evolves through different stages, and we are here to support our global team with a range of financial and non-financial rewards and benefits. Theres something for everyone! Here is an idea of what we offer: Competitive commission plan. Above market life insurance. Opportunities for development and professional growth. "Aerogen Connect" our employee-led program that helps our global teams unite and have fun. We donate 1% of profits and time to charities and organizations.

Role & responsibilities Precise refraction and accurate diagnosis Clear and precise case sheet documentation Patient Satisfaction by good and transparent communication and services To diagnose all patients on vision, eye diseases, vision disorder To do all diagnostic on equipment's in the hospitals under proper clinical protocol To record proper case details legibly and as per the clinical protocol To participate in outreach programs and academic events To volunteer in clinical/surgical emergencies To maintain the equipment's and accessories under possession with utmost care and self responsibility To assist all specialty clinics in rotation To start up and shut down the equipment required for specialty clinics and assist the doctor To coordinate with doctors in patient care and procedures To volunteer in internal scientific sessions, training programs and as faculty for optometry institute To counsel the patients or relieve the counsellor in case where required To coordinate with the counsellor regarding IOL lenses for surgery patients and to give the requisition to Centre Head as per requirement. Daily OP Report Optical prescription Report Contact lens advises, booking and dispensing report Checks the cleanliness in the optometry rooms Checks the optometry equipment's and in case of any problem immediately informs the Centre Head Interested applicants share resume on email: madhu.n@maxivision.in or WhatsApp at :9100223452 (Madhu-HR)

Responsibilities: * Perform cataract surgeries with phaco technology * Diagnose & treat retinal disorders through medical retina techniques * Perform Retina surgeries and opds

Responsibilities: Conduct eye exams using advanced technology Assist optometrist with contact lens fittings and dispensing Collaborate with ophthalmologists on patient care plans

Role Description This is a full-time on-site role for an Optometrist at Lenskart.com in Mysore. The Optometrist will be responsible for conducting eye exams, diagnosing and treating vision problems, prescribing corrective lenses, and providing guidance on eye care needs to patients. Qualifications Excellent communication and interpersonal skills B.sc/Diploma in optometry

At Dr. Agarwal s Eye Hospital, our values and overall mission are of utmost importance to... APPLY NOW Pediatric Ophthalmologist - Dr Agarwals Eye Hospital Pediatric Ophthalmologist At Dr. Agarwal s Eye Hospital, our values and overall mission are of utmost importance to us As an institution, we are unprejudiced by caste, color, social status, or religion Our belief in integrity, teamwork, and rewarding merit is unwavering and firm And we encourage every member of our organization to take ownership of every professional decision they take. Location: Karnataka - Karnataka - Mysore Non Doctors Full name Mobile Number Please input your primary mobile number so that our representative can contact you to confirm your appointment. Preferred Location LinkedIn Profile (optional) RESUME (PDF|DOC) Sharing reports from previous appointments will help the doctor give you a more accurate diagnosis. Maximum of 5 files can be uploaded and it needs to be in PDF format and should not exceed 5mb per file. Popular Searches Eye Hospitals - State & UT Eye Hospitals - City Diseases & Conditions Eye Anatomy & Treatments Blogs Categories Home Leads Need help clarifying your queries? We re here for you!