Responsibilities Responsible for execution of Central Report Review activities on the study based on the Monitoring strategy defined, with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. May support development of annotated visit reports such as PSV, SIV, IMV, COV & SCAN Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity. Document requested revisions and approvals in CTMS. Ensures these deliverables are provided according to company and/or sponsor specifications, including delivery deadlines. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations/special Sponsor’s requirements and pharmacovigilance issues documented in the report. Immediately communicates/escalates serious issues to Clinical Trial Manager/Project Manager Documents observations noted during reviews and ensures protocol deviations or action items are reported as necessary in appropriate systems for action by CRA/CM or other functional team members. May assesses CRA/CM report quality, risks, and trends as well as operational performance and summarizes the findings for CTM review and action planning. Participates in clinical monitoring/project staff meetings and attends clinical training sessions according to the project specific requirements. Involves in regular project discussion and email correspondence to maintain the most up-to-date project status knowledge and progression. Demonstrates understanding of other functions' roles in achieving compliance and delivery according to protocol, SOPs, ICH GCP and country regulations. May support in CTM activities such as Protocol Deviation management, Action Items management, etc.     Qualification & Experience Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience Should have 5+ years in Clinical Operations in Global CRO or Global Pharma. Should have 3+ years of CRA experience with on-site activities and PSSV, SIV, IMV, COV reports writing Having experience in phases II-III multicenter studies is preferred Must have worked on PSSV, SIV, IMV, COV reports review experience. Should have Good GCP knowledge Knowledge and experience in Medidata CTMS and Veeva TMF is a Plus Capable of working in an international environment skills  

Responsibilities Partner with the Departmental Leadership to create and deliver a robust global Regulatory Intelligence departmental strategy and plan for Syneos Health. Ensure that clinical regulatory intelligence is collected and maintained in Syneos Health Regulatory Intelligence System (RIS) Proactively evaluate and identify systems, automation, tools, and processes for tracking and reporting of Regulatory Intelligence Work closely with Country Subject Matter Experts (SMEs) from all/each region contributing to the overall understanding of the local regulatory landscape. Promote and ensure understanding with key stakeholder of the organization wide regulatory intelligence system, department purpose, deliverables and points of contact. Horizon scan, critically review and translate current and upcoming regulatory changes into clear internal strategic statement. Proactively engage and communicate with senior leadership representing the Regulatory Intelligence Department acting as a resource for technical knowledge and guidance making recommendations to support efficient and effective outcomes. Support the solutioning of escalations and proactively engage with internal stakeholders to remedy and reduce risk. Keep abreast of current data, trends, regulatory knowledge, developments and advances in the global regulatory environment. Support impact assessments of regulatory documents and guidelines on Syneos Health procedures as applicable and as assigned by management. Advise, consult and make final recommendations to all aspects of clinical regulatory intelligence. Identify and respond appropriately to issues and problems, providing innovative and effective solutions. Recommend and implement enhancements of Syneos Health Regulatory Intelligence processes to maintain the Regulatory Intelligence System Assume functional manager role for managers and staff in the Regulatory Intelligence department: Define, lead and oversee team operational plans. Ensure staff members fulfill their responsibilities in accordance with Regulatory Intelligence controlled documents and other relevant procedures. Communicates team / individual goals and expectations to ensure direct reports understand their responsibilities. Ensure performance and development processes and conversations are undertaken effectively. Monitor team resource capacity keeping FM informed about relevant trends or changes. Performs other work-related duties as assigned.   Qualification & Experience BA/BSc in related disciplines or regional equivalent or equivalent combination of education and experience. 8-10 years of industry experience within Regulatory Intelligence or Regulatory Affairs/Operations functions. Comprehensive regulatory knowledge and understanding of pharmaceutical and or medical device product development.  

Responsibilities Coordinates and supervises department operation. Stocking of nutrition products and other medications safely and properly and medicines are arranged from outside stores when it is required at emergency when the stock is not available in the in house pharmacy. Overseeing organizational medicine list and medical use Review annually medication list for the patient safety and efficacy Procurement of medicines Selection of good quality product To receive the quotation from the different company for the better rates to the organization. As per doctor requirements to check the comparative rates. Negotiation for scheme with supplier/manufacturer for the approved medicines Supervises departmental personnel including: hiring, orientation, determining workload and delegating assignments, training, monitoring, scheduling and evaluating performance, and initiative corrective and disciplinary actions. Prepares and dispenses medicines, chemicals and pharmaceutical preparations according to written orders by authorized medical practitioners with clinical privileges. Assist in selection, orientates, supervises, instructs departmental personnel. Initiates and implements Quality Improvement for the department. Preparing and assign duty and duty roster for the department staff Leading pharmacy committee Audit of medicines at nursing station for their expiry and storage condition Assisting assistant pharmacist in routine work whenever required Second check on gate pass Second check on the rates are properly supplied for the rate negotiated for the organization To forward the requisition for the medical head for making available of the new drug in the organization. To inform to the prescriber for non availability of the drug in the pharmacy through a written notification and suggested for substitutions. To check the expiries are returned to the supplier credit note is receive To check the invoices of the supplier are being forwarded for the payments To monitor the proper documentation for the narcotic drug purchase sales and storage To Internalizing the S.O.P Physical stock-taking of medicines quarterly   Qualification & Experience D-Pharma/B-Pharma Experience: 5-9 years . Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities Coordinate patient care by facilitating communication and collaboration between specialist doctors, primary care physicians, and other healthcare providers. Conduct patient consultations to assess medical conditions, provide appropriate medical advice, and recommend further diagnostic tests or specialist consultations, as needed. Assist in scheduling patient appointments with specialists and coordinate follow-up care, ensuring timely and efficient healthcare services. Collaborate with the Medyseva team to organize and conduct health camps, providing medical support and guidance to patients during these events. Educate patients about their medical conditions, treatment plans, and preventive care measures to empower them to take an active role in their health. Review and analyze patient medical histories and records, ensuring accurate and up-to-date documentation for efficient care coordination. Monitor patient progress and treatment outcomes, making adjustments to care plans as necessary to optimize patient health and well-being. Provide timely and clear communication to patients regarding their test results, treatment plans, and any necessary lifestyle modifications. Work closely with the Medyseva technology team to leverage digital healthcare solutions for improved care coordination and patient engagement. Keep up-to-date with medical advancements, guidelines, and best practices, applying evidence-based medicine in patient care and coordination. Collaborate with healthcare providers, both within Medyseva and external partners, to maintain a comprehensive network of specialists and resources for patient referrals.     Qualification & Experience Medical degree (MBBS) from a recognized institution, with a valid license to practice medicine. Proven experience in patient care, consultation, and coordination, preferably with exposure to digital healthcare solutions. Strong clinical knowledge and the ability to assess and diagnose a wide range of medical conditions. Excellent communication skills, with the ability to effectively interact with patients, specialists, and healthcare teams. Empathy and a patient-centric approach to healthcare, prioritizing patient well-being and comfort in all interactions.   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Responsibilities The Project Manager will be responsible for overseeing and managing multiple projects, ensuring their timely completion and successful delivery. The role involves coordinating with different teams. The Project Manager will be the primary point of contact for clients and will be responsible for maintaining strong customer relationships.   Qualification & Experience Experience in project management, Pharmaceutical industry. Strong organizational and multitasking skills Attention to detail and ability to prioritize tasks Excellent communication and interpersonal skills Ability to work in a fast-paced environment and meet deadlines Proficiency in project management CRO Experience in the testing or laboratory industry is a plus.  

Qualification & Experience Candidate should have experience of Nutraceutical/Pharmaceutical 5 to 7 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience Candidate should have experience of Nutraceutical/Pharmaceutical. with Tablet, Capsule, Soft gel, and Protein Powder. 20 -25 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"    

Qualification & Experience Candidate should have experience of Nutraceutical/Pharmaceutical. 8 - 10 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience GNM / B.sc Nursing 2 to 3 years of experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

Qualification & Experience B.Pharma 2 to 3 years of Experience   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"