1075 Pharmacology Jobs - Page 8

@7379843074 Pharmacology for Medical Colleges & Hospitals @ 7379843074 Positions - SR, AP, Associate Professor & Professor, Consultant Qualification- MD/DNB Location- Pan India Salary- Best in the industry. Contact / WhatsApp - 7379843074 (HR SHIKSHA) Email - hr13pathfinders@global.com Kindly share the same with your friends and colleagues. Also share your spouse CV if he/she is a doctor. Thanks & Regards (HR SHIKSHA)

Site Name: India - Karnataka - Bengaluru, Hyderabad Wework Krishe Emerald Posted Date: Jul 18 2025 Job Purpose: Provide scientific and technical expertise of the highest standards for local medical information, including interactions with Key External Experts (KEEs) and Key Opinion Leaders (KOLs) Provide medical and scientific input and information for business strategy for the region. Key Responsibilities : Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs) Plan, facilitate and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product specific campaigns and deliver scientific presentations with consistent messages for key products at these meetings, as required. Support and deliver scientific presentations with consistent “on label” messages at medical education meetings. Understand principles of and support Scientific Engagement (SE) activities as per Medical Plans. Have clarity in understanding on Scientific Engagements and Promotional Code. Become an expert in oncology where GSK have brands and support associated activities related to those brands. Be updated on scientific knowledge on oncology; GSK molecules and its PI to ensure its ‘On Label’ communications on various platforms. Support in feasibility assessment of potential research sites, develop concept notes, proposals, budgets, data collection and monitoring tools for field studies. Provide medical inputs into development and execution of brand strategy. Pharmacovigilance: Support Named Safety contact in strengthening of oncology Pharmacovigilance; ensure self-learning. Knowledge/ Education / Previous Experience Required Educational Background :- Minimum Level of Education - MBBS with post graduate qualification Preferred Level of Education - Post graduate qualification in Pharmacology / Public Health Why is this Level of Education Preferred - To interact with specialized HCPs Job-Related Experience:- Minimum Level Of Job-Related Experience Required Excellent written and oral communication skills in English, local language Experience of presenting scientific topics at different settings A sound understanding of the principles and practice of ICH-GCP and internal SOPs. Well-demonstrated ability to understand scientific methods and experimental design. 1-2 years in the pharmaceutical industry preferably in the oncology therapy area. Other Job-Related Skills/Background:- General Competencies Presentation skills at Scientific meetings Communication skills, both verbal and written Technical writing skills Keep up to date with new developments Ability to provide and receive constructive feedback Build and maintain relationships with colleagues Share knowledge with other team members Work as part of a team to reach common goals Deliver creative ideas for continuous improvement Develop good relationships with key opinion leaders Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way. GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable. If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing askus@gsk.com, so that we can confirm to you if the job is genuine.

CGC Landran is expanding its senior pharmacy faculty, especially in Pharmacy Practice and Pharmacology . Professor – Pharmacy Practice and Pharmacology Institution : CGC Landran, Mohali (Chandigarh Group of Colleges) Qualifications : PhD in Pharmacology and Pharmacy Practice , ≥ 12 years of teaching/research experience After PhD Minimum 8 Years experience of Teaching is mandatory. Send your updated resume to ankita.hr@cgc.edu.inFor any queries, contact us at 9875939971 Warm Regards Ankita Sharma SR. HR Executive ankita.hr@cgc.edu.in Chandigarh Group of Colleges, Landran, Mohali - 140307 (Punjab), India Job Type: Full-time Pay: Up to ₹90,000.00 per month Schedule: Day shift Education: Doctorate (Preferred) Experience: Professor (Senior Grade): 10 years (Preferred) Work Location: In person

CGC Landran is expanding its senior pharmacy faculty, especially in Pharmacy Practice and Pharmacology . Professor – Pharmacy Practice and Pharmacology Institution : CGC Landran, Mohali (Chandigarh Group of Colleges) Qualifications : PhD in Pharmacology and Pharmacy Practice , ≥ 12 years of teaching/research experience After PhD Minimum 8 Years experience of Teaching is mandatory. Send your updated resume to ankita.hr@cgc.edu.inFor any queries, contact us at 9875939971 Warm Regards Ankita Sharma SR. HR Executive ankita.hr@cgc.edu.in Chandigarh Group of Colleges, Landran, Mohali - 140307 (Punjab), India Job Type: Full-time Pay: Up to ₹90,000.00 per month Schedule: Day shift Education: Doctorate (Preferred) Experience: Professor (Senior Grade): 10 years (Preferred) Work Location: In person

Huron assists its clients in driving growth, enhancing performance, and maintaining leadership in their respective markets. Healthcare organizations are supported in fostering innovation capabilities and accelerating key growth initiatives, enabling them to shape the future rather than be disrupted by it. Collaboratively, clients are empowered to achieve sustainable growth, improve internal processes, and enhance consumer outcomes. Health systems, hospitals, and medical clinics face significant pressure to enhance clinical outcomes and reduce the cost of patient care. Merely investing in new partnerships, clinical services, and technology is insufficient to bring about meaningful change. To ensure long-term success, healthcare organizations must empower their leaders, clinicians, employees, affiliates, and communities to cultivate cultures that promote innovation for optimal patient outcomes. Joining the Huron team entails aiding clients in adapting to the rapidly evolving healthcare landscape, optimizing existing business operations, enhancing clinical outcomes, creating a more consumer-centric healthcare experience, and fostering engagement among physicians, patients, and employees throughout the enterprise. The role entails overseeing the day-to-day production and quality functions of a team of coders focused on achieving client production and coding accuracy goals. This includes planning, directing, supervising, evaluating feedback workflows, and coordinating activities among all coding staff within the team. Excellent communication skills, attention to detail, as well as strong technical and problem-solving abilities are crucial for success in this position. JOB DETAILS: - Assign accurate diagnosis and CPT codes in accordance with ICD-10 and CPT-4 coding systems for medical records - Code outpatient and/or inpatient records with a minimum accuracy of 96% and meeting turnaround time requirements - Exceed productivity standards for Medical Coding as per inpatient and/or specialty-specific outpatient coding norms - Uphold professional and ethical standards while focusing on continuous improvement to prevent revenue leakage and ensure compliance - Enhance coding skills, knowledge, and accuracy through participation in coding team meetings and educational conferences - Specialize in areas such as Inpatient, E&M, Acute, Ambulatory, Cardiology, Radiology, Pathology, Anesthesia, Emergency Room, Surgery, among others - Familiarity with CPT-4, ICD-9, ICD-10, and HCPCS coding - Interpret client requirements and project specifications to code charts accordingly - Adhere to prescribed coding standards like ICD-9/ICD-10 and CPT while ensuring accuracy and correctness of patient information - Assign appropriate medical codes to diagnoses and services, following client-specific guidelines and updates - Meet client productivity targets within specified timelines and deliver quality outputs - Prepare and maintain status reports QUALIFICATIONS: - Graduation in Life Science, Pharmacy, Physiotherapy, Zoology, Microbiology disciplines - Minimum of 2 years of industry experience - CPC (Certified Coding Professional) or CCS (Certified Coding Specialist) certification Position Level: Senior Analyst Country: India,

📌 Job Title: Subject Matter Expert – Nursing 📍 Location: Remote 🕒 Employment Type: Full-Time About Physics Wallah (PW): Physics Wallah is India’s leading EdTech platform, transforming access to quality education across competitive exams. As we expand our Nursing vertical , we’re looking for passionate and knowledgeable professionals who are eager to make a meaningful impact in the lives of future healthcare heroes. 💼 Roles & Responsibilities: As a Nursing SME, you will: Create top-quality academic content, including: Practice questions & mock tests Detailed solutions & study notes Align all content with current Nursing exam patterns (NORCET, AIIMS, Staff Nurse, etc.). Conduct doubt-clearing sessions and academic discussions when needed. Regularly review and update content based on latest exam trends and learner feedback. ✅ Requirements: Bachelor’s or Master’s degree in Nursing (B.Sc. / M.Sc. Nursing). Minimum 1 year of teaching or content development experience (preferred). In-depth knowledge of core Nursing subjects: Anatomy, Physiology, Pharmacology, Medical-Surgical Nursing, Community Health, etc. Ability to break down complex topics into simple, engaging explanations. Awareness of competitive Nursing exams is a strong advantage. 🌟 Why Join PW? Be part of India’s fastest-growing EdTech brand . Flexible work setup with a collaborative, mission-driven culture. Directly contribute to the success of thousands of nursing aspirants. Attractive pay package, aligned with experience and performance. Ready to Empower the Next Generation of Nurses? Apply now and become a part of PW’s growing Nursing team!

Should have knowledge in Clinical Data Managemen Should have good knowledge in edit checks crf design SAE Reconcilation crf annotation Good knowledge in Startup conduct phase and close out phase Required Candidate profile Strong understanding of clinical data management and E2b Guidelines Excellent clinical assessment and Communication Skills

Dear All, Greetings from Vivo Bio Tech Limited! Job Description: Business Development (BD) role** in a CRO setting Experience: 3+ Job Title:** Business Development Manager Preclinical Services Location:** Hyderabad Reports To:** Head – Business Development / Executive Director Job Overview: We are seeking a proactive and results-driven **Business Development Manager** to independently drive lead generation and conversion across domestic and international markets. The ideal candidate should have strong networking skills within the **CRO industry**, and proven experience in securing business from **Pharma, Agrochemicals, Industrial Chemicals, Vaccines, Generics, and Medical Devices** clients. This role requires working knowledge of **GLP compliance**, **regulatory affairs**, **toxicology studies**, and familiarity with submission processes to global regulatory bodies. Key Responsibilities:** * Independently generate, qualify, and convert leads for preclinical research services. * Submit tailored technical and commercial quotations to potential clients. * Network extensively across Pharma, Agrochemical, Vaccine, Generic Drug, Medical Device, and Chemical industries. * Understand client requirements and align them with organizational capabilities in **GLP and non-GLP studies**. * Develop and maintain strong client relationships to drive repeat and long-term business. * Coordinate with internal scientific and operational teams to design study proposals and timelines. * Provide market intelligence and competitor analysis to support strategic planning. * Track, monitor, and support **regulatory submissions** to international authorities such as USFDA, EMA, WHO, PMDA, ANVISA, etc. * Stay updated with global guidelines relevant to **Mammalian Toxicology**, **Ecotoxicology**, and **Regulatory Submissions**. * Promote services across **small and large animal studies**, including rodent, canine, minipig, and non-human primate models. * Collaborate on proposals for government and international grants or tenders (if applicable). Key Requirements:** * Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields. * Minimum 2–15 years of BD experience in a CRO or related preclinical research setting. * Strong understanding of **GLP requirements** and study types. * Working knowledge of **toxicology, pharmacology, ecotoxicology**, and **regulatory pathways**. * Familiarity with **GTC (General Toxicity Category)** studies and their scope. * Excellent communication, negotiation, and relationship-building skills. * Self-motivated and target-oriented with strong business acumen. * Willingness to travel domestically and internationally as required. --- Preferred Experience: * Exposure to **OECD, ICH, USFDA, EPA, REACH, and other regulatory guidelines**. * Experience in handling **multi-national clients** and long-term contracts. Vivo Bio Tech Ltd Survey # 349/A, Pregnapur Village, Gajwel Mandal. Siddipet District, PIN 502311,Telangana, India. Regards, Chandra Kanth | HRD chandrakanth.k@virinchi.com

About Alkem: Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally over 50 countries. We have consistently been ranked amongst the five pharmaceutical companies in India. Our portfolio includes illustrious brands like Clavam, Pan, Pan-D, and Taxim-O, which feature amongst the top 50 pharmaceutical brands in India. Job Purpose: To actively contribute to the organization/division by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors. To support the division medically in all activities related to the portfolio and provide high quality and timely service to internal and external stake holders. Responsibilities: To actively support development of promotion of allocated portfolio under supervision from the Line manager or the mentor, provide strategic inputs and support towards creation of marketing/brand plans/medical development plans, and towards design and execution of medical-marketing programs/clinical programs, including initiatives to enhance access to medicines Under supervision from the Line manager or mentor, create/review promotional, training, and Continuing Medical Education (CME) material in compliance with relevant industry codes and medical correctness In consultation with the Line manager or mentor, participate/facilitate/conduct customized promotional/educational interactions with Key Opinion Leaders (KOLs). These interactions include, but are not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, medical projects and studies In consultation with concerned stakeholders plan research projects and develop / review / approve protocol synopsis/final protocols/supporting documents per need Provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external (HCPs) customers, in adherence to relevant SOPs/policies Impart medical training to new sales staff on basic sciences/ TAs/assigned products. Provide refresher training to sales staff through ongoing training initiatives. Provide pre-launch and launch training to sales staff for new products Support New Product Evaluation (NPE), Marketing, and Business Development colleagues with medical evaluation and recommendations on commercial opportunities with new products. Support organization efforts at developing local formulations/line extensions through literature search/recommendations Support regulatory team by means of writing/revising/reviewing labeling documents for products as per relevant SOPs Support Pharmacovigilance activities by documentation and reporting of Adverse Events in a timely manner. Qualification : MBBS & MD Pharmacology (Mandatory) Experience : 1 to 4 years of experience in medico marketing

B.Pharmacy Freshers With SAS Training 2023 & 2024 Passouts Only are Eligible Must have Completed SAS Training With good Knowledge in SAS SDTM, Tables & Listing, Adams and Macros. Understanding of relational data base structure & data systems. Required Candidate profile Review protocols for completeness, appropriateness of clinical design and sound statistical analysis. Develop statistical analysis plans, including table, listing and graph specifications.

Education : MBBS & MD (Pharmacology) Strategic To manage, develop, implement and maintain policies and procedures and oversee the functioning of the Department in its entirety. In coordination with the management, formulate a strategy for the department for each quarter and the year. To participate in any strategic planning activities for AHI as defined by the management. To adhere to any set revenue targets that may be set for the Department. To keep Departmental expenses at a minimum within the limits of the budget, with goals to achieve reductions in expenses as defined. To ensure optimum utilization of facilities within AHI. To ensure qualitative and economic use of general supplies within AHI. Operational Provide support to clinical pharmacology department in review and associated activities such as pharmacovigilance, prescription monitoring and audit, formulary updation etc. Management of large datasets for analysis purposes, responses to health authorities, within agreed timeframes and to a high standard of accuracy, in compliance with JCI & NABH guidelines. Performs medical review of each and every single case report (OPD, IPD prescription monitoring, safety database etc). Author or Co-authors the medical literature of ICSRs/Case reports/AMR pattern including literature review. Assists in the preparation of other safety documents, as needed/required. Medical review of documents and check for consistency and accuracy of medical information across all documents. Assist pharmacovigilance team in writing narratives for AEs & ADR’s they process and feed into the database over vigiflow.

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, Mansi Verma WEPS SCO 12, LGF, Hollywood Plaza, VIP Road, Zirakpur, SAS Nagar, Punjab 140 603 Email: weps.hiring@gmail.com Mob: 07986969416

Job Title: Invivo Pharmacology scientist Job Location: Bangalore About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to companys integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Specific requirements for this role 1. Experience : 1-9 years 2. Demonstrated Capability: Thorough understanding and practical hands-on experience on Animal models of pain and arthritis 3. Education: Masters in Pharmacology /M.V.Sc Pharmacology Skills and Capabilities Hands-on experience in execution of neuropathic pain and arthritis models of rats and mice. Hands-on experience in handling surgical techniques like SNL (L5 and L6 or L5 alone), CCI, PSNL, SNI in both rats and mice. Hands-on experience in studies involving Diabetic neuropathy, Chemotherapy induced neuropathic pain, CRPS, Osteoarthritis, and Rheumatoid arthritis. Experience in handling & maintenance of instruments like Hargreaves apparatus, Dynamic plantar aesthesiometer, Incapacitance meter Analgesymeter, Von Frey filaments etc, and recording pain readouts using them. Will work independently or in association with senior scientists and other associates in the design and execution of in-vivo efficacy experiments in the relevant therapeutic area. Experience in animals handling (rodents and non-rodents) such as dosing by various routes, blood sampling by various routes, injections by various routes and surgical modalities which includes cannulation etc Associate to provide technical, analysis and reporting outcomes of research for projects in Neuropathic pain area. Ability to work consistently with cross functional teams to achieve common goals & ensure customer satisfaction. Demonstrate consistent ability to communicate with client in well-articulated manner and deliver the results within stipulated timelines. Organizational skills and the ability to work in a highly collaborative environment are required. Prior experience in people management is desired. Extended knowledge and understanding in various components of deliverables from supportive function such as DMPK, Exvivo, Safety assessment & Formulation department

Responsibilities: * Dispense medications accurately * Collaborate with healthcare team on treatment plans * Maintain inventory levels * Provide customer service to patients and staff * Assist pharmacists with clinical activities

The position of OECD GLP QA Auditor at Ribosome Research Centre in Kim is a full-time on-site role. As the GLP QA Auditor, your primary responsibility will be to conduct quality audits, ensure compliance with GLP regulations and guidelines, prepare audit reports, and recommend corrective actions. Your day-to-day tasks will involve reviewing study protocols, performing study-based inspections, facility-based inspections, and carrying out quality assurance activities. Additionally, you will collaborate with research staff to enhance quality management practices. To excel in this role, you must have prior experience in an OECD GLP environment. Proficiency in quality auditing, auditing skills, and quality management practices is essential. Strong written and verbal communication skills are also crucial for effective performance. A Master's degree in any life sciences field (e.g., Biotechnology, Pharmacology) is a mandatory qualification. Furthermore, your ability to work efficiently in a team-oriented environment will be key to succeeding in this position.,

Job Summary We are looking for a motivated and detail-oriented Clinical Audit Coordinator to support our Regulatory Quality & Compliance team. This is an ideal opportunity for recent graduates in Pharmacy, Clinical Research, Pharmacology, or Life Sciences to begin a career in clinical quality and regulatory audits. The role focuses on supporting audits conducted under GxP frameworks, including GCP, GLP, and GVP. ⸻ Key Responsibilities • Assist in planning, scheduling, and coordinating regulatory audits (GCP/GLP/GVP), including internal, external, sponsor, and regulatory inspections. • Support pre-audit document collection and preparation, including clinical trial documentation, SOPs, and training logs. • Help prepare audit materials: audit agendas, logistics checklists, and audit team communications. • Maintain and update audit trackers, audit logs, and regulatory compliance records. • Communicate effectively with cross-functional teams (clinical, pharmacovigilance, regulatory affairs, quality) to ensure timely responses and document submissions. • Assist in drafting audit summary reports, documenting findings, and tracking Corrective and Preventive Actions (CAPAs). • Support document archival and ensure adherence to ALCOA+ principles for data integrity. • Stay informed of evolving global regulatory requirements related to GCP, GLP, GVP, and data privacy (e.g., ICH, FDA, EMA, CDSCO). ⸻ Required Qualifications & Skills • Bachelor’s degree in Pharmacy, Life Sciences, Pharmacology, or Clinical Research. • Strong communication (written and verbal) and organizational skills. • Basic understanding of clinical trial processes, regulatory frameworks, and GxP principles. • Proficiency in Microsoft Office (Word, Excel, Outlook); exposure to quality or document management systems is a plus. • Strong attention to detail and ability to follow procedures with discipline and accuracy. ⸻ Preferred Attributes • Eagerness to learn and grow in clinical quality and regulatory compliance roles. • Exposure to GCP/GLP/GVP principles during coursework or internships is an added advantage. • Ability to handle confidential information responsibly and ethically. • A team player with a strong work ethic, problem-solving mindset, and adaptability in a fast-paced environment. ⸻ Benefits • Structured training in clinical quality and regulatory compliance. • Mentorship from experienced audit and quality professionals. • Career growth opportunities across QA, Regulatory Affairs, and Clinical Operations. • Dynamic and collaborative work culture focused on excellence and compliance.

REQUIRED PHARMACOLOGY SR AND ASSISTANT PROFESSOR. Who completed MBBS MD

We Have multiple Vacancy in K. J. Somaiya Medical College and Research Center and Hospital. Location: Sion, Mumbai Post: Associate Professor/Assistant Professor/Senior Resident/Medical Officer 1.Requirements: ASSOCIATE PROFESSOR: Department- COMMUNITY MEDICINE Department- GENERAL SURGERY Department-FORENSIC MEDICINE AND TOXICOLOGY Department-RADIOLOGY *Education UG: MBBS PG: Postgraduate, MS/MD,DNB in Subject Specialization. *Experience: One Year Experience as Senior Resident Four Year Experience as Assistant Professor * Research and Publication* Two Publication 2.Requirements: ASSISTANT PROFESSOR: Department-GENERAL SURGERY Department-FORENSIC MEDICINE AND TOXICOLOGY Department-RADIOLOGY *Education UG: MBBS PG: Postgraduate, MS/MD,DNB in Subject Specialization. *Experience: One Year Experience as Senior Resident 3.Requirements: SENIOR RESIDENT: Department-RADIOLOGY Department-COMMUNITY MEDICINE Department-MICROBIOLOGY Department-ANATOMY Department-BIOCHEMISTRY Department-PHYSIOLOGY Department-FORENSIC MEDICINE AND TOXICOLOGY Department-PHARMACOLOGY *Education UG: MBBS PG: Postgraduate, MS/MD,DNB In ANATOMY, PHARMACOLOGY, BIOCHEMISTRY, FORENSIC MEDICINE AND TOXICOLOGY, PHYSIOLOGY, MICROBIOLOGY *Experience: Fresher Can Apply. 4.Requirements: MEDICAL OFFICER: Department-COMMUNITY MEDICINE (UHTC) *Education UG: MBBS SALARY NEGOTIABLE. NOTE: Interested Doctors/Candidates kindly share your CV or Share Any reference who one is interested. Email ID : hr.somaiyamedicalcollege@somaiya.edu

Position: Medical Transcriptionist Location: BIMS Hospital, Bhavnagar Employment Type: Full-time Department: Medical Records / Documentation Job Summary: We are looking for a detail-oriented and experienced Medical Transcriptionist to join our healthcare team. The ideal candidate will be responsible for transcribing voice-recorded medical reports from doctors and healthcare professionals into written format, ensuring accuracy, confidentiality, and compliance with healthcare regulations. Key Responsibilities: Listen to and accurately transcribe dictations by physicians and other healthcare professionals. Review and edit transcriptions for grammar, clarity, and medical terminology accuracy. Ensure all documentation is in accordance with established hospital protocols and regulatory guidelines. Maintain patient confidentiality and data security at all times. Use electronic health record (EHR) systems to store and retrieve patient information. Communicate with medical staff to clarify information when necessary. Meet established turnaround times without compromising quality. Qualifications: Graduate in any discipline (science background preferred). Certification or diploma in Medical Transcription is desirable. Proven experience as a medical transcriptionist or in a similar role (preferred 1–2 years). Strong knowledge of medical terminology, anatomy, pharmacology, and diagnostic procedures. Proficiency in typing and transcription software. Excellent command of the English language (listening, reading, and writing). High attention to detail and ability to maintain confidentiality. Skills Required: Fast and accurate typing skills Sound knowledge of medical terms and abbreviations Familiarity with EMR/EHR systems Excellent grammar, spelling, and punctuation Strong time-management and organizational skills How to Apply: Interested candidates can share their updated CV at hr@bimshospital.com Or contact: +91-9016981981, 7227989814 Job Types: Full-time, Permanent, Fresher Pay: From ₹15,000.00 per month Benefits: Health insurance Paid sick time Paid time off Provident Fund Schedule: Day shift Fixed shift Morning shift Night shift Rotational shift Work Location: In person

Neurologist Required at Bathinda Punjab Salary 5 Lakhs Varanasi UP Salary 4 Lakhs Doctor couple can be adjusted in their respective branch

Company Description The SRM Medical College Hospital and Research Centre is located at Potheri in a 33.61-acre campus. The campus's strategic proximity to other institutions of the SRM Institute of Science and Technology facilitates collaborative research opportunities for staff and students. Position: Scientific Writer Role Description This is a full-time on-site Scientific Writer role located in Tamil Nadu, India. The Scientific Writer will be responsible for creating scientific content, conducting research, writing reports and articles, and collaborating with research teams to communicate complex scientific findings effectively. SRM CCP is seeking a motivated and detail-oriented Scientific Writer to support the development of high-quality research manuscripts and publications. The ideal candidate will have a strong background in scientific or medical writing, with experience in preparing manuscripts for peer-reviewed journals. Location: SRM Centre for Clinical Pharmacology (SRM CCP), SRM Institute of Science and Technology Eligibility: MBBS / PhD / PharmD Qualifications Strong scientific writing and research skills Ability to communicate complex scientific information clearly Experience in writing reports and articles Knowledge of medical or healthcare terminology Excellent attention to detail and work under minimal supervision Proficiency in data analysis and interpretation Should have published articles in scopus/pubmed indexed journals Experience: 1–2 years, with publications in Scopus-indexed journals Key Responsibilities: Draft, review, and edit scientific manuscripts, abstracts, and research reports Collaborate with investigators and research teams to ensure accuracy and clarity in content Ensure adherence to journal guidelines and publication ethics Maintain documentation and version control throughout the writing and submission process Salary: As per SRMIST norms Application Deadline: 25 July 2025 To Apply: Send your CV to srmccp.hiring@gmail.com This is an excellent opportunity for early-career professionals to contribute meaningfully to impactful research in a vibrant academic setting.

Your Tasks And Responsibilities Lead the clinical research medical science related activities such as preparation of synopsis, protocol, Clinical Study Report (CSR) and present the proposals in subjects expert committee (SEC) regulatory meeting. Collaborate with clinicians, KOL to get the feedback and inputs on clinical trial design, comparator and endpoints of the study to finalize synopsis. Review of patient eligibility and approval of patients through Interactive Response Technology (IRT) system Work with data management team to review data management plan, coding plan, SAE reconciliation, CRF completion guidelines, edit check specifications. Also, to ensure timely review of data extract and data cleaning activities to ensure timely database lock and release of tables, figures, and listings (TLFs). Coordinate with biostatistician to engage early with the study team to decide sample size, statistical analysis plan (SAP) apart from review of mock and/or blinded tables, figures, and listings (TFLs), and narrative and discussion planning for relevant documents Prepare risk assessment plan based on the protocol of clinical study to identify and address the safety and operation related risk specific to study protocol. Training the study team on protocol and applied aspect of the protocol to clarify the relevance and criticality of each activity considering the study endpoints. Interact with investigator to resolve the queries related with protocol from the sites and Ethics Committee. Medical monitoring activity which includes eligibility assessment based on inclusion, exclusion criteria and detailed medical history, review of study endpoint data review and safety investigations. Review of Adverse Events and Severe Adverse Events forms and provide review comments in timely manner. Planning publications activities for clinical journal manuscripts, abstracts submission for conferences, and subsequent review of posters/ oral presentations. Who You Are MD (Pharmacology) or other relevant medical qualification 2-6 years of relevant experience in the field of Medical Monitoring Experience in working in clinical science domain working in different capacities as medical monitor for clinical trial/ medical expert for clinical development plan for products across therapies is desirable. Job location: Sun House, Goregaon East, Mumbai

Experience from major pharma industries in Non-oral Products: Topical product and transdermal product. Experience in end-to-end topical product development activities for generic product development ANDA (Cream, ointment, gel, solution, lotion, foam, patch etc.) as well as NDA 505(b)(2), 505(b)(1). Experience in execution of lab scale manufacturing, reverse engineering, analytical know-how, plant level manufacturing activities; scale-up and exhibit batches based on quality principles QbD, QTPP, CQA, CMA, CPP, RA, FMEA. Experienced scientist to perform experiments for development of optimum prototypes (generic, non-infringing composition and robust manufacturing process) with diverse class of drugs & prodrugs (sensitive to pH, acid, base, temperature, oxygen, humidity). Experience in regulatory documentation CMC, MF, BMR, PDR, controlled correspondence for CMC, Biowaiver & Dossier preparation for US-FDA, EU-EMA, AU-TGA & DCGI through successful filing. Experience in working with cross-functional teams (ADD, MSTG, production, QC, QA, RA, IPC, PMO, BD, Microbiology, Pharmacology etc.) to achieve project goals - Filings and subsequent approvals. Knowledge and develop continuous understanding on competitive intelligence, due diligence, US-FDA quality concepts, statistics and global pharma trend analysis to support new product evaluation & introduction. Job Responsibilities To design, conduct and verify/review experiments to develop a robust formulation . To do literature search, patent search, prepare summary report and review. To prepare product development reports and protocols. To do product scale-up, exhibit batches and prepare reports for product filing and regulatory queries including post filling and post approval market queries. To prepare documents (i.e. PDR, CPD etc.) for regulatory submission Group work co-ordination. Project status report preparation. Experimental result review, interpretation and conclusion. To prepare technology transfer documents. To procure raw materials (API / excipients), packaging materials, innovator samples in consultation with packaging/purchase department. To do product validation, site transfer/change activities of products. To write Laboratory Notebook to enter details related to drug product manufacturing. To prepare test request for analysis of raw materials (API/Excipients) and Drug product.

Histopathology evaluation and report preparation of pharmacology studies Planning, designing and monitoring of GLP/Non -GLP toxicity studies in rodent and non-rodent Scientific data collection, interpretation of toxicology data and study report preparation/review.

The above post is open to all, however candidates from any category can apply for the post. Reservation for women will be as per University Circular No. BCC/16/74/1998 dated 10th March, 1998. 4% reservation shall be for the persons with disability as per University Circular No. Special Cell/ICC/2019-20/05 dated 05th July, 2019. Candidates having knowledge of Marathi will be preferred. The Educational Qualification, Experience & Pay-scale for the post of Assistant Professor is as prescribed by the University of Mumbai. AICTE from time to time. Please refer University Circular No. मशिमाक/ विशिमाक/तंत्र शिक्षण/ ११/ २०२०-२०२१ दिनांक ११ जानेवारी, २०२१ for qualifications and experience at the time of interview. Applicants who are already employed must send their application through proper channel. Applicants are required to account for breaks, if any in their academic career. Candidate should hold a B.Pharm and M.Pharm degree with 1st Class in either one of the degree SVKM’s Dr. Bhanuben Nanavati College of Pharmacy is one of the top most Pharmacy Institutes in the State of Maharashtra situated in Mumbai, Vile Parle West. Since 2004 it has achieved brilliance in pharmaceutical culture and research and has become a center of excellence in the field of pharmaceutical sciences. The college is affiliated to University of Mumbai and approved by the All India Council for Technical Education (AICTE), Pharmacy Council of India (PCI). At present the college conducts Four Year B. Pharm degree program which is accredited by national Board of Accreditation ( NBA) for full term of five years till 2022. In 2012, the college introduced two years course of M. Pharm with specialization in two streams Pharmaceutics & Quality Assurance to support higher education and research. In 2013, another M. Pharm course was introduced with specialization in Pharmacology. The college is an approved center for Ph. D program in Pharmaceutical Chemistry and Pharmaceutics. The faculty is actively involved in research activities including consultancy for national and international industries. More than 80% of the faculty holds a Ph. D degree and have industry experience ranging from 4-15 years. They have a strong industry connect because of which the college was selected for the AICTE-CII award. The college received the prestigious AICTE-CII best Industry-linked pharmacy institute Degree survey award 2015 and 2017. It was conferred the Platinum category in Pharmacy degree (standard) category for 2016. The college is Ranked All India NIRF ranking at 30 th Rank in Pharmacy college category for the year 2019. The College has won the BEST COLLEGE award for the 7 th time at the IPA-MSB organized Rx Festival. The college provides an open platform to the students to nurture and hone their academic skills, inculcate research trends and contribute to societal activities within their academic career of four years. The college focuses on pharmacy put into practice with the goal of strengthening the health care industry of the country which is booming. Though focused to ensure academic and co-curricular facilities to a vibrant student community, the college is conscious of its role as a constructive & responsible component of the larger society. The college conducts regularly guest lectures by Industry experts and career counselling sessions. Its consistent and unstinting efforts in this direction are borne out by the fact that students enter the college, young, immature, uncertain, bewildered, but leave its portal still young, but much more mature, self-confident professionals ready to lead rich lives of their own while enriching that of the society.