Clinical Operations Jobs

The Medical Superintendent is responsible for overseeing the clinical and administrative functions of a healthcare facility in Cuttack. This role requires a proactive leader who can manage medical staff, ensure quality patient care, and promote efficient operations within the hospital.Key Responsibilities:- Leadership and Management: Oversee the medical staff, including doctors and nurses, ensuring effective teamwork and collaboration for optimal patient care.- Quality Assurance: Implement and monitor policies and procedures that enhance the quality of care provided to patients, ensuring compliance with healthcare standards.- Budget Administration: Manage the hospital budget, allocating resources effectively to maintain a functional and efficient operational environment.- Patient Safety: Lead initiatives aimed at improving patient safety metrics, addressing any issues proactively to maintain health standards.- Staff Training and Development: Organize training programs for staff to enhance skills and knowledge, promoting a culture of continuous improvement.- Regulatory Compliance: Ensure adherence to all healthcare regulations and standards, facilitating necessary inspections and certifications.Required Skills and Expectations:Candidates should possess strong leadership and interpersonal skills, enabling effective communication with staff and patients alike. A solid background in healthcare management is essential, along with a thorough understanding of medical procedures and patient care protocols. Problem-solving abilities are critical, as the Medical Superintendent must navigate challenges and make informed decisions swiftly. Proficiency in budgeting and resource management is also required to support the hospitals financial health. Ideal candidates should have a minimum of 1 to 7 years of experience in a similar role, demonstrating a commitment to excellence in healthcare delivery.

Looking for Clinic assistant , Working Hours: 1:00 PM - 9:00 PMWorking Days: Monday to SaturdayManage front desk operations smoothly.Perform billing using clinic software (consultation, medicines, etc.).Maintain basic accounts and daily records.Coordinate with doctors and staff for patient flow.Ensure cleanliness, discipline, and smooth functioning of the reception area.Handle phone calls, WhatsApp messages, and patient enquiries.needs to know Hindi, English and Kannadabasic computer skillspatient care , need to do follow ups , review, if any pre salesneed to maintain records, medicine records, accounts,

General Manager - Matoshree Indirabai Baburao Sarnaik MBMC Hospital, Mira RoadAbout the OrganizationPlatinum Hospitals Pvt. Ltd. is one of Maharashtras leading multi-super speciality healthcare groups operating advanced PPP and private hospitals focused on affordable and cashless healthcare services.Our Hospital Network1. Matoshree Gangubai Sambhaji Shinde Hospital - Thane West2. Dharmaveer Anand Dighe Heart & Urocare Centre - Kalwa3. Freedom Fighter Hakim Ajmal Khan Hospital - Mumbra4. Ulhasnagar Municipal Corporation Super Speciality Hospital - Shahad5. Satya Sai Platinum Hospital - Ulhasnagar6. Platinum Hospital - Vasai7. Matoshree Indirabai Baburao Sarnaik MBMC Hospital - Mira Road8. Matoshree Indirabai Baburao TMC Hospital - Nalpada, ThaneAbout the HospitalMatoshree Indirabai Baburao Sarnaik MBMC Hospital, Mira Road is a multi-speciality hospital equipped with advanced ICU facilities, modular operation theatres, emergency services, diagnostics, and comprehensive speciality departments providing quality patient care.About the JobLeading overall hospital operations, clinical and non-clinical administration, manpower management, NABH compliance, quality initiatives, business development, statutory compliance, and coordination with municipal authorities to ensure efficient hospital performance.Eligibility* MBA Healthcare / MHA / BHA / Hospital Administration or equivalent qualification* Hospital administration experience mandatory* Strong knowledge of NABH, hospital operations, quality systems, budgeting, statutory compliance, and team management* Excellent leadership, communication, and decision-making skillsExperience* 5 - 9 Years of hospital management experienceLocationMatoshree Indirabai Baburao Sarnaik MBMC HospitalMira Road East, MaharashtraSalary60,000 - 90,000 per month based on qualification and experience.Apply NowInterested candidates may send updated CV or contact HR Department immediately.

We are looking for a dedicated and motivated Clinical Assistant to join our team in Tiruchirappalli. This is a full-time position suitable for recent graduates or those with limited experience in the field. Key Responsibilities:- Patient Interaction: Assist patients with their check-in process, ensuring they feel comfortable and informed about their visit. This involves answering questions and providing necessary information.- Clinical Support: Help healthcare professionals with basic clinical tasks, such as taking patient histories and measuring vital signs. This support is crucial for efficient patient care.- Documentation: Maintain accurate and up-to-date patient records, including charts and files. Proper documentation ensures continuity of care and compliance with health regulations.- Equipment Handling: Sterilize and prepare medical instruments and tools for use in examinations and procedures. Proper handling ensures patient safety and a clean working environment.- Communication: Liaise between patients and medical staff to facilitate clear communication. This helps in understanding patient needs and improving service delivery.Required Skills and Expectations:- A Bachelors degree in a relevant field (B.Sc) is essential. This educational background provides the foundational knowledge required for the role.- Strong communication skills are necessary to interact effectively with patients and the medical team.- Attention to detail is important for accurate record-keeping and ensuring patient safety.- A willingness to learn and adapt to new tasks in a busy clinical environment will be highly valued.- Basic knowledge of medical terminology can be advantageous but is not mandatory.

Qualification Requirements: Current Coding Certification (CPC, CPC-P, CPC-H, CPC-I, CRC, CCS) through AAPC and/or AHIMA. Minimum of 5 years coding experience with specific knowledge of Medicare and Commercial RiskAdjustment such as Hierarchical Condition category (HCC) Additional experience in facility (OPPS/IPPS) coding experience is preferred Additional experience in Health Plan Risk Adjustment Data Validation Audit (RADV) experience ispreferredExperience and Skills: Ability to work independently in a fast-paced remote environment with minimal supervision andguidance Ability to interact with management and remote coding personnel Possess strong organizational skills and attention to detail Ability to adapt to changing priorities while managing a wide range of projects Adaptive and flexible to new ideas and change Advanced knowledge of medical terminology, anatomy and pharmacology Advanced skills utilizing official coding resources for research and problem solving Advanced skills and knowledge of computers, use of required software to perform job functions Excellent written and communication skills and the ability to explain complex information

Essential Functions Review and assure the quality, integrity, accuracy, and completeness of clinical trial data based on project specific guidelines. Develop and maintain a library of effective data quality checks. Review data exports and reports to identify, investigate, and reconcile data discrepancies with Clinical Operations staff and/or clients Data Managers. Prepare, review, and upload appropriate Data Management documents to the Trial Master File Perform thorough development testing of the datasets prior to release to production, inclusive of creating test scripts and execute testing as applicable. Author Data Transfer specifications (DTS) for incoming and outgoing data files. Collaborate effectively and build productive relationships across the global operations team. Performs other job-related duties as assignedQualifications 3+ years of data management experience in the clinical trials industry BS/BA degree or professional experience equivalent. Demonstrated successful experience in all relevant clinical data management activities in a Pharmaceutical or CRO setting. Working knowledge of clinical trial research, including FDA, GCP/ICH guidelines, GDPR, CDISC/SDTM standards and 21 CFR Part 11 Experience working with EDC systems, e.g., Medidata Rave or Oracle Inform Familiarity with industry wide coding dictionaries such as MedDRA is a plus Experience with relational databases and XML a plus Excellent written and oral communication skills. Excellent analytical and problem-solving skills Ability to function independently. Ability to prioritize and handle multiple tasks and projects concurrently

Job Description: Should be responsible for preparation of qualitative medical writing deliverables in any therapeutic area Should have good experience in scientific and regulatory writing (Protocol writing, CSR, Manuscript, Abstract, Review articles and Medico-marketing inputs) Should be able to develop LBL, Poster, News-letters, KOL cases, booklets, atlas, guideline booklet, product monographs, calendars, compendium, customized journals, handbooks, conference abstract booklets, yearbooks, KOL opinion booklets, case studies, CMES, etc. Should have hands on experience in literature search and systematic review Should be accountable for medical writing deliverable and should ensure work on assigned projects adheres to industry/international standards Should be able to draft article on Health Economic Outcome Research and understanding on subject will be added advantage Should be responsible for continual improvement of in-house medical writing capabilities Should have an excellent understanding of all aspect of ICH-GCP; keen insight on external clinical publication practices and standards. Should liaise with internal team, clients, authors and KOLsExperience: Min 4 - 7 years experienceQualification: Bachelors degree / Masters Degree in any Pharma / Lifesciences/ Science related field. Excellent verbal and written skills (English). Good organizational, interpersonal, and team skills. Ability to deliver results under pressure. Goal oriented, self-motivated; able to work independently but within a team environmentDesired Skills/Experience: A good understanding of the healthcare market, challenges, growth prospects and healthcare delivery operations Strong customer and contact network in healthcare domain A minimum of three five years medical writing experience within the pharmaceutical industry or a contract research organisation. Able to work independently, initiate their own projects as needed to streamline their wo

Organizing Kick-off meetings with the client co-ordination with the functional Head. Responsible for allocating the project/Study to team members. Responsible for Review and Internal approval of Data Management Plan (DMP), Case Report Form (CRF), and Edit check Specification Document (ESD). Responsible for Review and Internal approval of Data Entry Guidelines, Self-Evident Correction Document (SEC). Internal approval of Annotated CRF (aCRF) and Functional Design Specification (FDS) Document. Responsible for preparing and training the SOPs. Responsible for approval of database screens, Edit checks designed in database and DCF/Query tracker. Internal Quality Control for all Data Management Documents like Data Management Plan, Annotated CRF, Functional Design Specification Document, and Edit check Specification Document. Responsible for Issuing the Database Test Certificate. Responsible for Database Lock and Unlock procedures. Responsible for exporting the data to SAS team for analysis. Responsible for Review and approval of Master Data Management File (MDMF). Responsible for Data Management Presentation in Investigator meeting. Providing inputs for proposal development in co-ordination with the Function Head.