200 Mpharm Jobs - Page 3

You are required to have a professional qualification such as MSc in Life Science, MPharm, BAMS, BHMS, MBBS, along with experience in medical writing. Excellent communication skills and a good understanding of clinical research are essential for this role. Your responsibilities will include preparing and editing medical and scientific manuscripts and abstracts, as well as producing and publishing peer-reviewed scientific papers and presentations that explain the results of clinical studies. You should possess good communication skills and have a thorough understanding of editing and regulatory processes and requirements. If you meet the qualifications for this position and are interested in ...

As part of our global team, you will have the opportunity to explore, break barriers, and innovate with science and technology in the fields of Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about enriching the lives of people, customers, patients, and the planet. We are always seeking curious minds who are willing to imagine the unimaginable with us. In the Healthcare sector, our purpose is to help create, improve, and prolong lives through the development of medicines, intelligent devices, and innovative technologies in areas such as Oncology, Neurology, and Fertility. Joining our Healthcare team means becoming part of a diverse, inclusive, and flexibl...

As a potential candidate for the position, you should hold a commerce graduate degree along with an MBA in Marketing. Alternatively, a BPharm/MPharm qualification with expertise in international regulatory affairs and the preparation of CTD Format Dossiers would be suitable for this role. You should possess a minimum of 4-5 years of experience in the pharmaceutical industry, with a preference for experience in international marketing. Familiarity with international marketing practices within the Pharma sector is required, with a minimum of 3 years of relevant experience. This position is based in Sector 8, Noida, and falls under the categories of full-time, permanent, and fresher job types. ...

CorroHealth Hiring Fresher's Eligibility Criteria:- -Work Location - Kochi -Graduation - Only(B. pharm, M. pharm)Life science Graduates can also apply No Diploma "Note - No Nursing / No BPT" -Graduation Percentage - Minimum 60% and above -Medical Coding Certificate - Non Mandatory -Work Mode - Work From Office WALKIN INTERVIEW For more details you Can Connect to below mentioned Contact number & Email Contact - 8778691270(Whatsapp) Email -damaris.davisjayakumar @corrohealth.com

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Priya 9600450980 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS Hr Rubini-9600405840 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Pharmacy, Bpt, Nursing Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM Staff Nurse GNM Perks and benefits Incentive Up to 5k Insurance Provident Fund

We are looking for a highly skilled and experienced Pharmacist to join our team at MAX Hospital in Noida. The ideal candidate will have 3 to 8 years of experience in the pharmaceutical industry, with a strong background in pharmacy practice. Roles and Responsibility Dispense medications to patients and provide counseling on their proper use. Manage inventory and maintain accurate records of prescriptions and dispensing activities. Collaborate with healthcare professionals to develop and implement medication therapy plans. Conduct patient assessments and monitor their response to medication therapy. Develop and implement pharmacy protocols and procedures. Participate in quality improvement in...

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols. Should have knowledge in Clinical Data Management EDC Edit Checks SAE Reconcillation Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

You should ideally hold a B.Pharm or M.Pharm degree, with a preference for an MBA qualification. It is required to have a minimum of 1 to 2 years of field experience in a pharmaceutical company, particularly in executive and managerial roles. For managerial positions, a minimum of 2 years of experience in the same capacity is mandatory. The role necessitates possessing conceptual skills, analytical abilities, and creativity. Your responsibilities will include formulating plans and ensuring the successful implementation of strategies in the field. We provide an attractive remuneration package along with incentives for the right candidate. To apply for this position, please email your resume t...

As a Research and Development Officer at Cosmetics Concept Research (CCR), you will play a vital role in the creation and enhancement of innovative Dermaceutical, cosmeceuticals, skincare, haircare, baby care, and men's grooming products. Your responsibilities will include conducting research, developing new formulations, and improving existing products. You will be based in Ahmedabad, India, working on-site to ensure the quality and performance of each product meets rigorous standards. Utilizing your strong research and analytical skills, you will collaborate with cross-functional teams to analyze data and bring new ideas to the table. Effective communication and adherence to safety protoco...

As a Project Manager at our company, your primary responsibility will be to build, engage, and grow the assigned community through digital marketing and various organizational initiatives. You will be tasked with developing and implementing campaigns and communication strategies for different marketing channels. Your role will involve connecting and engaging with doctors within the community, aiming to develop them as influencers. Additionally, you will be required to coordinate with the internal medical team, key opinion leaders, and influencers to align relevant medical content. Collaborating with medical associations relevant to the community will also be a key aspect of your responsibili...

We have urgent vacancies for pharmacist and sr. pharmacist for TATA 1 mg @Bigbasket in Chennai. Job Description Designation: Pharmacist & Sr. Pharmacist Job Locations- Mugalivakkam, Navalur, Medavakkam, Virugambakkam, Thoraipakkam, West Tambaram Key Responsibilities: . Customer support and prescription validation . OTC order processing and clarification calls . Inventory and order management . Picking, packing, and handover to delivery riders . Cash-on-delivery (COD) cash handling . Root Cause Analysis for delayed orders . Stock receiving, audits, and shrinkage control . Store operations and manpower coordination . End-to-end store and customer fulfillment management Preferred Qualifications...

Job description Education: Should be D.Pharma or B Pharma ( Ayurveda specialised). Experience: Minimum 2 years of Ayurveda Hospital Pharmacy experience. Position: Pharmacist (OP & IP) . Location - Noida sector 62 8448519870

The candidate will undergo a self-financed job-oriented patent analyst training at the Indian Institute of Patent and Trademark. On successful completion of the training, they will be placed for full-time patent analysis in the pharmaceutical domain. Required Candidate profile Scientific and Analytical Thinking Eager to work in drugs and formulation Candidates must have sound knowledge about the subjects they study in Graduation

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols Recruit, screen, and enroll study participants while maintaining accurate documentation and records Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Clin Infotech is offering the internship opportunity for BDS MDS Dental Graduates Should have Knowledge in Pharmacovigilance Should Have knowledge on Argus & MEDDRA Applicants Should Complete Certification in Pharmacovigilance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Clin Infotech is offering internship Opportunities for B.Pharm and M.Pharm Freshers who are willing to start a career in Clinical Research Pharmacovigilance clinical data management sas Medical writing and Medical coding Required Candidate profile Clinical Research Internship includes of Hands on Experience on softwares in Clinical Research Pharmacovigilance clinical data management Domain. B.Pharm M.Pharm and Pharm D Are Eligible to Apply

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Urgent Walk in For M.Pharmacy fresher Completed Clinical Data Management Training only Eligible CDM Certification is Mandatory Knowledge of Clinical Data Management Plan, study phase conduct phase and Close out phase Required Candidate profile Strong knowledge of cGMP and relevant regulatory requirements: This includes understanding manufacturing processes, quality control procedures, and validation requirements.

This position requires a sound knowledge of medical coding and the denial management process for multiple specialties. Applicants must be proficient in ICD-10 and CPT medical coding and have obtained a Certified Professional Coder (CPC) credential Required Candidate profile Should have strong knowledge In Medical Coding Anatomy Physiology and Medical Terminology Should have Good Communication Skills

Walk-In Interview for BDS/BHMS/BAMS/ BPT/ BSC/MSC( Nursing) Fresh Graduates For Medical Coding Non Certified Freshers Only Applicants should have good knowledge in Medical Coding Anatomy and Medical Terminology Required Candidate profile Candidates Should have good knowledge in Medical Coding ICD 10, Anatomy Medical terminology and CPT Exposure to CPT-4, ICD-9, ICD-10, and HCPCS coding

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Perform triage & intake of ICSR received daily in ARGUS databases within the agreed timelines Processing literature, spontaneous clinical trial and solicited cases Responsible for coding events, indications and patient history based on MEDDRA Required Candidate profile EDUCATION: M.Pharm/Pharm D/Life sciences / Microbiology / Biotech /Biochem /Nursing / BDS EXPERIENCE: Strong Knowledge in pharmacovigilance With Certification or its equivalent.

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.