112 Healthcare Services jobs in India

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Job Details

To author, review, and independently manage high-quality clinical documents: Clinical Study Reports (CSR) including narratives, Protocol, and Informed Consent Form (ICF), Investigator Brochure.

Review and Preparation of regulatory documents as per country-specific regulatory requirements. Clinical Trial Documents (CTD) Modules (2.4, 2.5, 2.6, 2.7)

Excellent skillset in literature search, understanding of PICOS criteria and PRISMA statement

Contribute to the planning of data analyses and presentations to be used in CSRs; Ensure compliance with documentation

Excellent data interpretation skills.

Understanding of ICH-E6 and E3 guideline.

Understanding of other ICH and regulatory guideline required for drug development.

Understanding of template for Protocol as per ICH-E6 and Transcelerate Common trial protocol

Basic understanding of statistics

.

Relevant Experience and Education

Postgraduate in Pharmacy (Pharmacology), Life Sciences

7-12 years of experience in core medical/regulatory writing

Ability to manage multiple projects and meet tight deadlines.

Attention to detail and strong analytical skills.

Excellent written and verbal communication skills

What Cencora offers

Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.

Full time

Affiliated Companies

Affiliated Companies: PharmaLex India Private Limited

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimageable with us.

**Associate Clinical Trial Supply**

Clinical Trial Supply is a global team of Clinical trial Supply Managers and Coordinators with offices in Germany, Japan and China. This year we are going to futher diversify our way of working adding a team of Clinical Trial Supply Associates located in India.

In the role of a Clinical Trial Supply Associate, you will be responsible for supporting the global Clinical Trial Supply team in the execution of clinical trial supply chain activities e.g., ensuring GxP compliant documentation for the certification of investigational medicinal products by a qualified person or in preparation for inspections by authorities.

**Responsibilities**:

- Support the coordination and management of clinical supply projects, including planning, scheduling, budgeting, and resource allocation.
- Archiving of clinical supply documentation in internal and external GMP and GCP systems ensuring clinical supply documentation meets GxP standards for inspection purposes.
- Organize and control the compilation of documents for approval by the competent person.
- Check (content and completeness) and archive technical specifications, documents, and contract annexes.
- Manage project documentation, including project plans, status reports, and meeting minutes.
- Create and review supply contracts and control budget/invoices approvals within the defined framework. Escalate issues as necessary.
- Support post-trial reviews and identify opportunities for process improvement.
- Assist the Clinical Supply Manager and Coordinator with other project-related tasks as required.
- Ensure full GMP compliance and documentation for clinical supply activities, including returns, destruction, and full global traceability of Investigational Medicinal Products.
- Participating in project meetings and providing support to coordinate project activities.
- Develop and maintain effective relationships with internal and external partners.
- Preparing project reports, presentations, and other project-related documents.

**Requirements**:

- Bachelor's degree in a scientific or related field.
- Extensive knowledge of English with a good command of the technical vocabulary. Excellent communication skills, both verbal and written, with the ability to communicate effectively with stakeholders at all levels.
- 1-2 years of experience in clinical supplies management or other related fields in the pharmaceutical industry e.g., Manufacturing, Quality Control, Quality Assurance, Regulatory Affairs Logistics or Clinical R&D.
- Understanding of GxP and other regulatory requirements related to clinical supplies.
- Strong attention to detail and a focus on delivering high-quality results.
- Excellent analytical and problem-solving abilities with the ability to work collaboratively in a fast-paced and dynamic environment.
- Detail-oriented, organized, and able to work independently and as part of a team.
- Proficient in Microsoft office tool suite (Word, Excel, and PowerPoint).
- Strong attention to data management skills with a focus on quality of documentation.
- Must be self-motivated with the ability to manage multiple tasks, prioritize, and meet tight deadlines.

**What we offer**:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimageable with us.

**Expert Clinical Trial Supply (Team Lead)**

Clinical Trial Supply is a global team of Clinical Supply Managers and Coordinators with offices in Germany, Japan, and China. This year we are going to further diversify our way of working adding a team of Clinical Trial Supply Associates located in India.

Leading a team of Clinical Trial Supply Associates, you will be ensuring high quality and timeliness of the work of your team by providing clear direction, guidance, and support to team members. Focus of the team is supporting the global Clinical Trial Supply team in the execution of clinical trial supply chain activities e.g., ensuring GxP compliant documentation for the certification of investigational medicinal products by a qualified person or in preparation for inspections by authorities.

**Responsibilities**:

- Supervise and support a small team of CTS-Associates and ensuring high quality and timeliness of the work of your team.
- Provide clear direction, guidance, and support to team members, ensuring they understand their roles and responsibilities.
- Ensure full GMP, GDP and GCP compliance of the work of your team
- Collaborate with the team of Clinical Trial Supply Coordinators to manage the clinical supply chain for assigned clinical trials with a focus on ensuring documentation meets GxP standards for inspection purposes.
- Develop and maintain effective relationships with internal and external partners
- Provide support to other members of the Clinical Supplies team as required
- Collaborating with the team on different projects
- Participating in project meetings and providing support to coordinate project activities
- Creating and maintaining project tracking tools
- Preparing project reports, presentations, and other project-related documents
- Handling project-related administrative tasks
- Assisting in the management of project budgets, timelines and ensuring completion of deliverables within budget and time constraints
- Ensure adherence to study budget and escalate issues as necessary
- Other duties as assigned
- Support global clinical supply chain process improvements
- Assist in the maintenance of complete and accurate clinical supply documentation, including batch record review and reconciliation

**Requirements**:

- Bachelor's degree in a scientific or related field
- Extensive knowledge of English with a good command of the technical vocabulary. Excellent communication skills, both verbal and written, with the ability to communicate effectively with stakeholders at all levels.
- 3-4 years of experience in clinical supplies management or other related fields in the pharmaceutical industry e.g., Manufacturing, Packaging, Quality Control, Quality Assurance, Regulatory affairs, Logistics or Clinical R&D
- Experience in participation and leading project teams in the clinical, clinical supply or CMC environment
- Detailed knowledge of international GMP, GDP and GCP rules, and other regulations related to Clinical Trial Materials
- Strong attention to detail and a focus on delivering high-quality results.
- Excellent analytical and problem-solving abilities
- Ability to work collaboratively in a fast-paced and dynamic environment
- Highly motivated, self-starter with the ability to work independently
- Proficient in Microsoft office tool suite (Word, Excel, and PowerPoint)
- Strong attention to data management skills with a focus on quality of documentation
- Must be self-motivated with the ability to manage multiple tasks, prioritize, and meet tight deadlines.

**What we offer**:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Greetings from Vijaya Diagnostic Centre,

We are looking for PRE (Patient Relationship Executive) for Hyderabad & Bangalore

Roles and Responsibilities:

• Guide the customer for the required services and ensure their comfort in all the processes.
• Check patient readiness for requested tests. Like adequate fasting and etc
• Q-Line Management, Managing Token System for comfort of customers at billing counters
• Helps the customers in selecting packages for different tests and explains them about precautions and timings
• Ensure that all the customers are guided properly to undergo the tests within specified time
• Ensures that Collected samples reaches to the central laboratory as per the Existed Logistics route plan.
• Follow-up on samples dispatched with the processing center
• Keep a tab on report delays if any and promptly inform the concerned about the same
• Arrange for home delivery of MRI/CT/NM reports for patients convenience
• Collaborate with other branches in case of emergency service breakdowns, to transfer patients with minimum fuss

Support billing desk during staff shortage

Role:  Other Hospital Staff - Other

Industry Type:  Medical Services / Hospital (Diagnostics)

Department:  Healthcare & Life Sciences

Employment Type:  Full Time, Permanent

Role Category:  Other Hospital Staff

Education

UG:  Any Graduate

Skills Required
Patient Care, Hospital Administration

Posting Date

07/17/20252340 North Highway 7, North Vernon, Indiana, 47265, United States of America

DaVita is seeking a Patient Care Technician who is looking to give life in an outpatient dialysis center. You can make an exceptional difference in the lives of our patients and their families dealing with end-stage renal failure or chronic kidney disease. Do you desire to deliver care in an empathetic, compassionate way - the way you'd want your own care to be?

If you haven't considered Nephrology before, read on as we think that you should.

This is a Monday/Wednesday/Friday Unit

hours are generally 4am to 6pm

Joining DaVita as Patient Care Technician (PCT) is an exciting opportunity to jump start your career in the health care industry! With paid, extensive training, you will gain the skills needed to care for our patients and build a network of other health care professionals across the geography where you live. Once you have successfully completed training, you will join a holistic team of care professionals – including nurses, dietitian, social workers, and other experienced PCTs – to care for our patients. It's not a job, it's giving life and a career based on passion and purpose.

DaVita – which is Italian for "giving life" – is working to provide quality service to patients, partners, and teammates. Our mission is to be the Provider, Partner, and Employer of Choice.

Our PCTs also find DaVita professionally fulfilling. To help advance your career, we offer clear paths to higher levels of responsibility and compensation through our Clinical Ladders program. Through DaVita's Bridge to your Dreams program, teammates who have been in their role for six consecutive months and in good standing, are eligible to receive tuition assistance up front to pursue their dream of becoming a DaVita RN and getting their Associates Degree in Nursing. We also have dedicated training to become a Facility Administrator, and training to become a Regional Operations Director. Your success is driven by your performance and desire.

Some details about this position:

No Dialysis experience is required.

Training may take place in a facility or a training clinic other than your assigned home clinic

Potential to float to various clinics during and after your training

You must have a flexible schedule and be able to work mornings, evenings, weekends, and holidays

What you can expect:

Direct Patient Care. Spend the majority of your day in direct one-on-one patient care to provide safe, comfortable and hygienic dialysis treatment.

Our PCTs care for multiple patients.

Technician Duties. To monitor patients before, during and after dialysis treatment including measuring and recording stats, patient observations, and hemodialysis machine setup. Please note you will have exposure to blood and needles.

Building long-term relationships with your patients who are suffering from end stage renal disease and are receiving treatment on average 3 times/week. You will also be responsible for educating patients on Kidney Dialysis related topics.

Team. Cross functional team of clinicians including technicians, nurses, dietitians, social workers and leadership. PCTs work under the supervision of a RN.

What we'll provide:

DaVita Rewards package connects teammates to what matters most including:

Comprehensive benefits: Medical, dental, vision, 401(k) match, paid time off, PTO cash out

Support for you and your family: family resources, EAP counseling sessions, access Headspace®, backup child and elder care, maternity/paternity leave, pet insurance, and more

Paid training

Requirements:

Desire to enter the health care field to care for other people in need

High school diploma or equivalent

Must be comfortable working around blood and needles

Must be comfortable mixing acid or bicarb

Physical and mental ability to work long hours (some shifts are 12+ hours) on your feet so wear comfortable shoes! Our work ends when it's safe for our patients.

Willingness to train and work across multiple clinics within the territory as needed.

Health care experience a plus including: BONENT Certified, Certified Hemodialysis Technician (CHT), Certified Nursing Assistant (CNA), Certified Medical Assistant (CMA), or Phlebotomy certification.

DaVita is a clinical leader! We have the highest percentage of facilities meeting or exceeding CMS's standards in the government's two key performance programs. We expect our teammates to commit to improving patient health through clinical goal setting and quality improvement initiatives.

Ready to make a difference in the lives of patients? Take the first step and apply now.

#LI-BS1

At DaVita, we strive to be a community first and a company second. We want all teammates to experience DaVita as "a place where I belong." Our goal is to embed belonging into everything we do in our Village, so that it becomes part of who we are. We are proud to be an equal opportunity workplace and comply with state and federal affirmative action requirements. Individuals are recruited, hired, assigned and promoted without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, protected veteran status, or any other protected characteristic.

This position will be open for a minimum of three days.

Salary/ Wage Range

For location-specific minimum wage details, see the following link:

Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies and experience. DaVita offers a competitive total rewards package, which includes a 401k match, healthcare coverage and a broad range of other benefits. Learn more at

Colorado Residents: Please do not respond to any questions in this initial application that may seek age-identifying information such as age, date of birth, or dates of school attendance or graduation. You may also redact this information from any materials you submit during the application process. You will not be penalized for redacting or removing this information.

Appointment Scheduling and Coordination:Schedule diagnostic tests (., blood tests, X-rays, MRIs) based on doctor referrals or patient requests.Coordinate timing between multiple diagnostic departments to streamline patient visits.Confirm appointments and follow up on rescheduling or cancellations.Patient Registration and Documentation:Assist patients with registration and ensure all necessary documentation (referral forms, prescriptions, ID proofs) is complete.Collect patient history relevant to the diagnostic procedure (., allergies, fasting status).Maintain accurate electronic medical records (EMR).Pre-Test Guidance and Instructions:Inform patients about test preparation requirements (., fasting, hydration, medication restrictions).Provide clear instructions for specialized tests like contrast-enhanced imaging or stress tests.Ensure informed consent is obtained when required.Liaison with Diagnostic Technicians and Pathologists:Communicate test orders and priorities to the relevant lab/radiology staff.Ensure timely sample collection, scanning, or imaging procedures.Follow up on test results and their dispatch to patients or referring physicians.Patient Support and Service:Assist elderly, disabled, or anxious patients with care and comfort.Address patient queries related to procedures, waiting times, or results.Ensure a clean, welcoming, and stress-free diagnostic environment.Billing and Insurance Coordination:Verify patient insurance and eligibility for diagnostics services.Generate cost estimates and facilitate payments or reimbursements.Liaise with TPA (Third Party Administrators) for cashless claims where applicable.Result Delivery and Reporting:Monitor the timely availability of reports and inform patients once ready.Deliver soft or hard copies of test results as per patient preference.Coordinate with doctors for any urgent or abnormal findings requiring immediate attention.Compliance and Quality

Experience

1 Years

No. of Openings

2

Education

B.A, B.C.A, B.B.A, B.Com, BDS

Role

Patient Care Coordinator

Industry Type

Hospitals / Medical / Healthcare Equipments

Gender

( Male / Female )

Job Country

India

Type of Job

Full Time

Work Location Type

Work from Office

Face interview location

SRMS FIMC- CP 2/3, Lohia Path near Fly Over, Vishwas Khand, Gomti Nagar, Lucknow, Uttar Pradesh

Roles & Responsibilities

(Defines the prime focus areas of the job)

Patient Care Management

Receive patients with warmth and provide a comfortable atmosphere for assessment and treatment.

Provide info related to services and tariff to the patients.

Orients and educates patients and their families by explaining the care plans and other information relating to the treatments.

Pre and post-counseling for the patients undergoing the treatment plans if required.

Address and resolve patient complaints and concerns promptly and effectively.

Understand and action accurate data entry on a daily basis

Handling Appointments

Understand the CRM platform

Comprehend detailed nuances around therapist availability and accordingly block appointments

Maintain data related to financial transactions, patient flow, and individual patient visits.

Track patient's journey from lead status to discharge and follow-ups

Patient Experience Enhancement

Respect patients by recognizing their rights; and maintaining confidentiality.

Collect patient testimonials and feedback as per organizational policy.

Monitor and evaluate patient care metrics, identifying areas for improvement.

TAT of 30 mins to be adhered for all the calls received

Coordination and Collaboration

Responsible to follow up on the assessment report till it gets delivered to the patient

Work closely with the sales team to promote patient care initiatives and success rate

Increase in conversion ratio will be reviewed in constant interval

Quality Improvement

Monitor delivery of care by documenting; identifying progress toward desired care outcomes; intervening to overcome deviations in the expected plan of care; and reviewing the care plan.

Job Location: Indira nagar / Malleshwaram

Detailed Job Responsibilities:

• Ensuring that every patient in the clinic is made to feel comfortable and cared for during their first visit and thereafter every appointment.

• Assisting patients in filling forms required by the Doctor for the first consultation, by explaining to them components that they are unclear about.

• Understanding from patients their chief concerns, their history and providing the doctor with all the relevant information to ensure that the Doctor has a better understanding of the patient

• Educating patients in simple words the treatment approach, the pricing in details, the expected recovery and all other details enabling patients to make an informed decision

• Ensuring that all sales interactions are done in a patient-centric approach

• Assuring patients basis their diagnosis, treatment prescription on their recovery and convincing them to take the treatment program; including sharing success stories, cracking barriers and involving the Doctor where needed to clarify clinical doubts

• Convincing patients to commit to the treatment program and ensuring they complete it to experience recovery

• Establishing a tone of empathy that helps to resolve any patient complaints or conflicts

• Prioritize patient satisfaction throughout the patient journey to build long-term relationships

Collaborate with calendar management team to optimize scheduling and streamline patient interactions

• Ensure a professional and well-maintained appearance personally and collaborate closely with doctors, housekeeping staff, support functions, and other team members to keep the clinic premises welcoming and to create a patient-centric environment

• Responsible for day-to-day operations & overall financial performance of the clinic

• Maintain counselor reports daily

• Coordinating with finance department (Invoices, Getting Discount Approval, Billing)

Qualifications & Skills:

• HSC/Graduate

• Must know Microsoft Excel

• Previous experience in patient counseling, customer service, or related roles, with a focus on grooming

• Proven sales experience and the ability to meet or exceed sales targets

• Excellent interpersonal and communication skills, with a genuine passion for patient care

• Software Efficiency

Skills Required
Sales Experience, Customer Service, Microsoft Excel, patient counseling

? We're Hiring! ?
Medybiz Pharma , Bangalore is looking for passionate individuals to join us as Patient Care Executives!

If you have a background in healthcare, excellent communication skills, and a commitment to patient well-being, we'd love to hear from you , Freshers can also Apply ?

? Location: Bangalore / Office ?
?️ Working Days: 6 days a week
CTC: 3 LPA
Qualification: B.Sc / M.Sc in Nutrition or related field
Languages - Hindi , English and Kannada (Mandatory)

? Send your resume to:
(HIDDEN TEXT)

Skills Required
Patient Care, Nutrition