711 Pharmacology Jobs - Page 27

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. / / / / - , 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.

We require doctors for Medical Colleges & Hospitals PAN India Qual: MD/MS, DNB, (All Dept) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Mamta Call/Whatsapp: 8708568683 weps.placement@gmail.com

We are seeking a highly motivated and compassionate recent graduate to join our clinical team as an Entry-Level Clinical Assistant/Clinical Associate. This is an excellent opportunity to gain hands-on experience in a clinical setting and contribute to patient care or clinical research. You will work closely with physicians, nurses, and other clinical staff, assisting with various tasks related to patient care, data collection, and administrative support. This role is ideal for individuals with a strong interest in healthcare and a desire to learn and grow in a dynamic environment. Responsibilities: Patient Care Support: Assist with patient intake and vital sign measurements. Prepare examination rooms and ensure they are clean and stocked with supplies. Provide basic patient support and comfort. Assist with the administration of basic medical procedures under supervision. Clinical Data Management: Accurately collect and record patient data in electronic health records (EHR) or clinical research databases. Assist in the preparation of clinical reports and data summaries. Maintain accurate and organized clinical records. Ensure data integrity and confidentiality. Administrative Support: Schedule patient appointments and manage patient flow. Answer phone calls and respond to patient inquiries. Assist with filing, photocopying, and other administrative tasks. Maintain inventory of clinical supplies. Clinical Research Support (if applicable): Assist with the recruitment and screening of clinical trial participants. Assist in the administration of study procedures and data collection. Maintain study documentation and regulatory files. Ensure adherence to study protocols and ethical guidelines. General Support: Assist clinical staff as needed. Participate in team meetings and training sessions. Maintain a clean and organized work environment. Any other duties as assigned. Qualifications: Bachelor's degree in a Life Science, Healthcare, or related field (e.g., Biology, Nursing, Psychology, Public Health). Strong interest in patient care or clinical research. Excellent communication and interpersonal skills. Strong attention to detail and accuracy. Ability to work independently and as part of a team. Strong organizational and time-management skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Must be a recent graduate.

We are seeking a highly motivated and detail-oriented recent graduate to join our Drug Safety team as an Entry-Level Drug Safety Associate. This is an excellent opportunity to launch your career in the pharmaceutical industry and contribute to the safety surveillance of our products. You will gain practical experience in various aspects of drug safety, including adverse event processing, data entry, and safety reporting. This role is perfect for individuals with a strong interest in drug safety and a desire to learn and grow in a fast-paced environment. Responsibilities: Adverse Event Case Processing: Receive, triage, and accurately enter adverse event reports into the drug safety database. Ensure timely and accurate data entry in compliance with company Standard Operating Procedures (SOPs) and regulatory guidelines. Assist in the follow-up of adverse event reports to obtain complete and accurate information. Perform quality control checks on case data to ensure accuracy and consistency. Data Management and Safety Reporting: Assist in the preparation of safety reports and data summaries. Maintain accurate and organized drug safety records. Assist in the tracking and monitoring of adverse event trends. Learn to identify and escalate potential safety signals. Regulatory Compliance: Develop a basic understanding of global drug safety regulations and guidelines (e.g., ICH guidelines). Adhere to company SOPs and regulatory requirements. Assist in the preparation of regulatory submissions. General Support: Assist in the maintenance of drug safety databases and systems. Participate in team meetings and training sessions. Support senior drug safety staff as needed. Perform other duties as assigned. Qualifications: Bachelor's degree in Pharmacy, Pharmacology, Life Sciences, Nursing, or a related healthcare field. Strong interest in drug safety and pharmacovigilance. Excellent attention to detail and accuracy. Strong organizational and time-management skills. Ability to work independently and collaboratively within a team. Good communication and interpersonal skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Must be a recent graduate. Preferred Qualifications (but not required): Basic understanding of medical terminology. Familiarity with drug safety databases or systems. Coursework related to pharmacology or drug safety.

Profile- Associate Professor Radiologist Location – Gaya (Bihar) Hospital Name- Medical College & Hospital Number of Bedded- 650 Number of Year- New Setup CTC- 3.5-4 Lacs Qualification- MD About Hospital: About: New Hospital and medical college, started in january 2025. Going for LOP. Applying For 150 MBBS Seats New Departments: Anatomy, Physiology, Biochemistry, Pharmacology, Pathalogy, Microbiology, FMT, Community Medicine, General Medicine, Pediatrics, Derma, Psychiatry, General surgery, Ortho, ENT, Opthal, Gyne & Obs, Anasthesia, Radiology, Dentistry Nearest Airport: Gaya International Airport- 27 km Nearest Railway Station: Gaya Junction- 36 km Specialist Requirments: Vacancy of Radiologist as Associate Professor & 1 as Professor Assoc- 3.5 to 4 LacsProf- 4-5 lacs-*Male/Female Both can do-*Duty Hours: Mon to Fri- 9 AM to 4 PM (OPD timings)Sat- Half Day- 9 AM to 2 PMIf living in campus 24/7 doctor required as emergencies are there-*Sundays Off-*Accomodation provided in campus*For AP, ASP & professor hospital is okay to buy out the Notice period of candidate Job Type: Full-time Pay: ₹350,000.00 - ₹400,000.00 per month Work Location: In person

Job description Greetings From You & I Consulting ! You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. *Hurry Do Not Miss This Opportunity To Work For Global Giant MNC. We are hiring for the below locations under Medical Reviewer Role!! *Locations :-*Chennai *Mode Of Interview - Walk-In (*Call or Whtsapp Now our HR Specialist:- @ puja - 8250242229 for details) *Mode Of Work :- Work From Office * CTC Upto - 12 To 24Lpa *Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app) PFB Job Insights for Medical Reviewer Role!! Author a CCC for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. Detail any requests for changes to the case, including the narrative. Skills required:- Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills * * *Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app) *Note:- *Though We Try and Answer The Calls Immediately, but Due to Heavy Call Flow The Below Numbers Might Be Busy At Times. In case you find the number busy, please whatsapp your details to us in the below format: - Name- Mobile number - Mail - Qualification - Total work experience - Current Organization- Location - Last CTC Expected CTC:- *Interested candidates can even refer their friends or relatives provided the criteria *FOR interview Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app)

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy Years of Experience: 1 to 3 years Language - Ability: English(International) - Advanced What would you do? Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases. What are we looking for? Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases. Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualifications Bachelor of Pharmacy

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations. Key Responsibilities: Study Coordination: Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements. Site Management: Assist in site selection, initiation, monitoring, and close-out activities. Documentation: Maintain accurate and complete study records, including case report forms, source documents, and regulatory binders. Communication: Facilitate effective communication between study sites, sponsors, investigators, and internal team members. Data Management: Ensure timely and accurate data collection, entry, and query resolution. Regulatory Compliance: Ensure compliance with all applicable regulations, guidelines, and standard operating procedures. Patient Recruitment: Support patient recruitment and retention efforts. Training: Provide training and support to study staff on study protocols and procedures. Quality Assurance: Participate in quality control activities and internal audits. Qualifications and Skills: Education: Bachelor's degree in life sciences, nursing, or a related field. Experience: Fresher or recent graduate with a strong interest in clinical research. Knowledge: Basic understanding of clinical research principles and Good Clinical Practice (GCP). Skills: Excellent organizational, communication, and interpersonal skills.

Help us bring cutting-edge medical treatments to life! Become a key player in clinical research and accelerate advancements in healthcare. Opportunities We offer two paths into the exciting world of clinical research: Internship: Get a hands-on introduction to clinical trials through a time-bound internship program. Ideal for students or recent graduates eager to experience the field. Fresher-Level Position: Launch your career as a Clinical Research Coordinator! This position offers ongoing employment for those committed to this exciting field. Regardless of path, you'll get to: Manage the flow of clinical trials: Oversee study logistics, participant documentation, and ensure the study progresses smoothly. Be a meticulous record-keeper: Collect and safeguard essential research data with the highest industry standards. Champion safety and ethics: Protect patient rights and ensure all research practices are ethical and compliant. Work within a team of like-minded professionals: Collaborate with investigators, healthcare providers, and fellow research enthusiasts. Qualifications Internship: Enrolled in or a recent graduate of a degree program in life sciences, health sciences, nursing, or a related field. Fresher-Level Position: Recent graduate with a degree in life sciences, health sciences, nursing, or a related field. For both: Passion for research, detail-orientation, strong organizational skills, clear communication, and willingness to learn. What We Offer Hands-on experience: Jumpstart your career or get real-world training. Training and mentorship: Get guidance from experienced researchers in the field. Professional development: Access resources or company-sponsored coursework to enhance your potential. Competitive compensation: Interns receive a stipend; fresher-level position offers salary and benefits. A role at the forefront of medical innovation: Shape the future of healthcare.

Refer Medical Records and assign ICD-10-CM, CPT, HCPCS Codes Clinical Documentation Review Medical Coding and Medical Billing

Job description: Responsibilities: Perform routine and non-routine tests and analyses using the appropriate technical equipment and instruments Assisting the Faculty/students in conducting practicals and practical exams. Daily checkup and maintenance of Laboratory equipment Practice safe work habits, including complying with all safety, health, and environmental rules and regulations Maintain and ensure the safety and proper functioning of the instruments under their care Maintain records of equipment usage and service schedules. Maintain equipment in proper working order and maintain a clean work area Maintaining the Stock records Any other duties assigned by the higher authority We are looking for Lab Technician who can handle and maintain the Lab with Proper knowledge. Excellent organizational skills Ability to perform physically demanding work such as moving and lifting equipment, standing for long periods of time, etc. Computer skills: knowledge of Microsoft Office and other relevant computer programs. Analytical and numerical skills: ability to perform mathematical calculations (add, subtract, multiply, divide) in different units of measurement; ability to use concepts such as fractions, percentages, and ratios.

Hiring experienced Medical Professionals for our multispecialty hospital in Purnia, Bihar. Accommodation provided. MD (Anatomy, Physiology, Biochemistry, Microbiology, Pathology, Forensic Medicine, Community Medicine, Pharmacology)

Urgent requirement our Clint Job Profile : QA , QC , CRA , RA , R&D , Pharmacist , Medical Billing , Medical Record summarization , Medical Reviewer , Clinical Research EXP : 0 to 4 Years Salary : 18 to 5 L Job Locations - Pune , Mumbai, Goa. Required Candidate profile BSc , MSc , D.Pharm , B.Pharm, M.Pharm , all pharmaceutical , health care , life science ,heath care IT , CRO Background candidates required fresher & experienced

Job Title : Associate Professor / Professor Department : College of Pharmaceutical Sciences Institution : Rama University , Kanpur Location : Mandhana , Kanpur Position Type : Full-Time role Position Summary The College of Pharmaceutical Sciences at Rama University seeks a dynamic and dedicated individual for the position of Associate Professor/Professor in the Department of Pharmaceutical Sciences. The successful candidate will have a strong academic background, a passion for teaching, and an active research agenda that will contribute to the growth of the department. This is an exciting opportunity to work in a highly collaborative environment with world-class faculty and contribute to advancing pharmaceutical science education, research, and practice. Key Responsibilities Teaching and Curriculum Development : Teach undergraduate, graduate, and professional courses in Pharmaceutical Sciences, including but not limited to pharmacology, pharmaceutics, medicinal chemistry, and pharmaceutical biotechnology. Develop, implement, and evaluate course content, lecture materials, and assessments. Mentor and advise students, including supervising graduate students in their research projects and theses. Participate in curriculum development and improvement within the department to ensure the program meets the latest advancements in pharmaceutical sciences. Research and Scholarship : Establish and maintain an active research program in an area of pharmaceutical sciences. Publish research findings in peer-reviewed journals and present at national and international conferences. Seek external funding through grants and partnerships to support research initiatives. Collaborate with colleagues within the department and across disciplines to foster research innovation and advancement. Service and Leadership : Contribute to the development of the departments goals, strategic plans, and initiatives. Serve on departmental, college, and university committees as assigned. Participate in professional organizations and activities related to pharmaceutical sciences. Provide leadership in service learning and outreach activities within the community and the profession. Administrative and Professional Development : Participate in academic advising and student recruitment. Attend departmental meetings and contribute to the administrative responsibilities of the department. Engage in ongoing professional development to stay current in the field and contribute to the advancement of pharmaceutical sciences. Required Qualifications Ph.D. in Pharmaceutical Sciences, Pharmacology, Medicinal Chemistry, Pharmaceutics, or a closely related field from an accredited institution. For Associate Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with a strong track record in teaching, research, and service. For Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with demonstrated leadership in research, teaching, and professional service. Demonstrated expertise in one or more areas of pharmaceutical sciences (e.g., drug development, pharmacology, medicinal chemistry, clinical pharmacology, pharmaceutics, etc.). A strong record of peer-reviewed publications and external research funding. Experience in teaching at the undergraduate or graduate level, including course development and delivery. Strong communication skills and the ability to mentor students and collaborate with colleagues. Preferred Qualifications Post-doctoral experience in a relevant area of pharmaceutical sciences. Experience in obtaining federal, industry, or foundation research funding. Evidence of leadership in professional organizations, research teams, or educational initiatives. Experience in interdisciplinary collaboration and industry partnerships.

To monitor the proper drug usage and preparation mostly for anti cancer drugs To manage extravasations immediately and to keep the details of these untoward events. To give regular rounds to all patients, who are getting chemotherapy in day-care facilities as well as in-patient. To see the Hospital protocols are properly followed on each case basis and to do necessary changes if deviation is there. To attend tumour board meetings and documentation work must be thorough The chemotherapy drugs before dispensing should be checked with prescription. The brands which are written on the prescription or told by the Consultants should not be changed without the permission of the concerned consultants. All the chemotherapy drugs should be prepared inside the preparation chamber In the ward, should give regular rounds with consultants. Any uncommon side effect seen in any patient, after giving chemotherapy drugs, should be recorded by the clinical pharmacologist. Monitoring prevention of extravasations. Any other allotted tasks. Preferred candidate profile Pharm D. Interested candidates can DM on 6359603615 alternatively can email with updated resume on hr@kdhospital.co.in

Job description Brief Job Description -Research associates conduct desk-based research (incl. clinical, scientific, regulatory, commercial, etc.) on assigned topics and generate a concise summary of findings. They are expected to keep abreast of new developments in their assigned therapeutic area/s and report new events/updates to their respective team members. They are also strongly encouraged to include critical and analytical thinking into their deliverables. Candidate - Highly enthusiastic and committed individuals with strong desk-based research skills are sought for this position Candidates are expected to be meticulous, thorough and well organized. They should be quick learners, have an excellent work ethic and should be willing and able to work in a rapidly evolving role/environment Candidates are expected to possess excellent communication skills, both written and oral The position offers a rare opportunity to be mentored by seasoned industry professionals within Vyuhgenics. Responsibilities - This is a full-time, desk-based job in our Bangalore, India office The primary focus will be on collection, collation and curation of scientific, clinical, regulatory and commercial evidence about therapeutic areas, products, markets, companies and customers of relevance to the global biopharmaceutical industry Travel to scientific and clinical symposia and conferences may be offered to promising candidates Additional skills - Excellent English language skills and working knowledge of MS Office (Word, Excel, PowerPoint) or Google Docs.

Hiring SR/AP Professor Ophthalmology Pediatrician General Medicine Surgeon Orthopedic Gynecology Emergency Medicine Anesthesia Community medicine Radiology Pharmacology Forensic Biochemistry Physiology for Medical College in Jaipur & Udaipur

As a Senior Medical Advisor , you will play a critical leadership role in shaping and executing the medical affairs strategy for our diabetes portfolio, while leading a high-performing team of Medical Advisors . Your responsibilities will span from managing the scientific landscape to driving the success of new product launches, ensuring that both the medical team and our organization are aligned with global standards and regulatory requirements. You will also play a key role in advancing scientific knowledge and supporting cross-functional collaboration. Key Responsibilities: Strategic Leadership : Develop and implement comprehensive strategies for the launch of new products/indications , including KOL engagement , medical education , and scientific outreach. Real-World Evidence Generation : Lead real-world evidence (RWE) generation activities in close partnership with affiliate medical teams , regional , and global colleagues to address data gaps and improve clinical and commercial outcomes. Stakeholder Collaboration : Engage proactively with professional associations, KOLs , and other key stakeholders to build and promote scientific advocacy for your assigned therapy area (TA) and product portfolio. Medical Education & Scientific Dialogue : Drive medical education initiatives and foster ongoing scientific dialogue to enhance the knowledge base of healthcare professionals, collaborating with internal teams across clinical , regulatory , and commercial functions. Publication Leadership : Identify opportunities for publication projects such as secondary analyses , review articles , and independent publications to bridge data gaps and meet medical advocacy objectives. Regulatory & Compliance Support : Work closely with regulatory affairs to ensure compliance of promotional materials and product packaging with relevant regulatory laws and guidelines. Organizational Readiness & Advocacy : Facilitate organizational readiness for new product launches, ensuring that both internal teams and external stakeholders are well-prepared, in collaboration with regulatory and commercial teams . Regulatory & Clinical Operations Support : Provide expert medical insights and strategic support to assist in regulatory submissions , presentations , and approvals for indication expansions and new product approvals . Qualifications & Experience: MBBS, MD/MS in Pharmacology , or equivalent (preferred) from a recognized institution. A minimum of 5 years of industry experience in medical affairs , preferably with a focus on diabetes or related therapeutic areas. Strong scientific expertise in diabetes and an in-depth understanding of product portfolios in this therapeutic space. Proven ability to lead and manage teams effectively, developing a high-performance culture among Medical Advisors . Excellent collaboration skills with both internal and external stakeholders, along with strong communication skills (written and verbal) to effectively disseminate scientific data. Highly developed strategic thinking and analytical abilities with a proven track record of managing complex medical situations and translating them into actionable insights. A creative and innovative mindset , with the ability to drive initiatives to successful completion and ensure operational excellence.

JIMSH is hiring for Asst. Prof., Asso. Prof. Professor in Anatomy, Physiology, Pharmacology, Forensic Medicine, Paediatrics, Dermatology. Please share your resume to the following email ID:hr@jimsh.org/ or may call : +91 9230932814 Required Candidate profile MD + relevant exp. at per with the NMC regulations.

India's No. 1 IT Company is Hiring for Medical Reviewer MBBS/MD Graduates with 1 yr to 5 yr Experience in Clinical Trials, PV, ICSR, SUSAR, Clinical Trial Operations Salary up-to 18LPA Call-Prachi-8287816038/ Rukhsar- 9899875055

To receive the patient / customer with a smile and greet them To maintain good relations with customers/doctors To receive and transcribe prescriptions from customers and advise the dosage of medicines to the patients and give counseling if required Required Candidate profile Education : D Pharmacy / B Pharmacy

Vacancies for SR /Asstt. Prof/Associate Prof/Professors Specialities: Anatomy Physiology Biochemistry Pharmacology Forensic Medicine Community Medicine General Medicine Pediatrics Surgery Orthopedics Anaesthesiology etc. etc.. Whatsapp 8558958087

Fresher Hiring 2021 - 2024 Passouts only - All India Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Role & responsibilities Perform data reconciliation between different data sources and study documents to ensure data integrity and consistency across datasets. Generate data queries to address discrepancies, inconsistencies, and missing data identified during data review, ensuring timely resolution and documentation of data queries Communicate data queries to investigative sites, data managers, and study personnel, following up on query responses and resolving discrepancies in collaboration with relevant stakeholders Identify deviations from protocol-specified procedures, eligibility criteria, and data collection guidelines, escalating issues to appropriate personnel for resolution Perform quality checks and data validation procedures to ensure accuracy, consistency, and reliability of clinical trial data, adhering to data management standards and industry best practices Assist in the development and implementation of data validation plans, data review guidelines, and quality control procedures to maintain high standards of data quality and integrity. Assist in a variety of specialties including but not limited to primary care, orthopedics, rheumatology, etc. Updates patient history, physical exam, and other pertinent health information in the document as required. Complies with Compliance standards of the Organization as laid by HIPAA. Performs other duties and tasks to improve provider productivity and workflow as assigned by supervisors. Assist documenting the patients, electronic health record (EHR). Fresher Hiring - Pharma / Life Sciences / Medical Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Location - All India - Delhi, Mumbai, Pune, Bangalore, Kochi, Chennai, Hyderabad, Ahmedabad, Bhopal, Indore, Kolkata, Chandigarh

Refer Medical Records and assign ICD-10-CM, CPT, HCPCS Codes Clinical Documentation Review Medical Coding and Medical Billing

MD Medicine required at Azamgarh UP ICU Experience Preferred Salary 4 to 4.5 Lakhs + Accommodation Jhajjar Haryana Salary 3.5 to 4 Lakhs + Accommodation Mankachar Assam Salary 4 to 4.5 Lakhs + Accommodation Required Candidate profile Talaja Bhavnagar Gujarat Salary 3.5 to 4 Lakhs Bhiwani Haryana Salary 3.5 to 4.5 Lakhs As per Experience Bathinda Punjab Salary 3.5 Lakhs + Accommodation Minimum 3 years Experience Required