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  • Active Jobs Found
    (Last Updated: Jan 29, 2023)
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Clinical Specialist

AbbVie

Full time
  • 2+ years
  • Not Disclosed
  • Delhi, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 2+ years
  • Not Disclosed
  • Delhi, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Responsibilities Clinical Specialists for Facial Aesthetics Responsible for clinical training of HCPs, medical education, CMEs and other training initiatives within the zone Closely interact with the doctors and clinically facilitate them for performing BOTOX® and Juvederm™ procedures Closely work with the sales team and coordinate with them meeting their clinical facilitation needs Develop new injectors in conjunction with the sales team for respective zones Engage the HCPs on scientific discussions and product differentiation Drive execution of all regional and national medical education programs in close coordination with the sales team Take accountability for Zonal sales of the listed doctors Active involvement in all the training initiatives, ensuring compliance with the laid down SOPs and processes Daily reporting and weekly/monthly/quarterly reviews with the line manager   Qualification & Experience B.Pharma/ M.Pharma/ BDS 2-5 years of Sales/Training/ or clinical specialist experience in pharmaceuticals or healthcare sector with good command over English language and scientific terminology Candidate with executive presence, excellent presentation skills and communication skills.  

  • pharma
  • clinical research
  • pharmacovigilance

Medical Lead Oncology

Novartis

Full time
  • 1+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Feb 23, 2023
  • 1+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Feb 23, 2023

Responsibilities Support country medical affairs strategy in line with the global strategy, country insights and market conditions, and implementation of Medical Affairs activities within the designated therapy area(s). Coordinate scientific meeting, symposia, congresses, Continuous Medical Education (CME) and other medical / scientific exchange and engagement activities which could bring value to the therapy area; develop engagement plan(s) for country customer-facing activities and events, and ensure timely execution of the activities in an efficient and compliant way. Ensure enquiries are responded to in a quality, timely manner, and in accordance with applicable standards; establish response documents for frequently asked questions. Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies / clinical research within the therapeutic area. Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities. Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for partner engagement and events are tailored to local needs, and reviewed/approved per local/P3 guidelines. Ensure medical insights are provided to cross-functional groups, including, but not restricted to: Pharmacovigilance, Regulatory Affairs, Market Access, QA, Commercial and Brand team and others. Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities.   Qualification & Experience MBBS; MD Mandatory with min 1 year industry experience Operations Management and Execution Project Management Collaborating across boundaries Clinical Trial Design, Data & Reporting Medical Science and Disease Area Knowledge Medical Education and Scientific Engagement Non-Interventional Studies (NIS) / Epidemiology Studies Medical Governance and Medical Safety  

  • clinical research
  • mbbs
  • MD

Associate - Regulatory Affairs

Colgate-Palmolive

Full time
  • 1+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 1+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Responsibilities Work closely with and support Regional Regulatory Affairs programs and activities for new product registration and life-cycle management of CP portfolio, including but not limited to, product renewals, variations, notifications and/or new license applications. Support the regulatory strategy defined at Regional and/or Global level, and report regularly the progress to Regional Regulatory Affairs Department with relevant important metrics, particularly in terms of timelines, the status of encouraging data required from other functions and dossier preparation. Compile documents and information required for high quality and successful submissions, license renewals and annual registrations, and maintenance of product registration dossiers for authorities. Assist the Regional Regulatory Affairs Department in preparing submissions to Proficient Authorities and Notified Bodies, ensuring timely approval of new products and life-cycle submissions. Track outstanding documentation and advise the relevant Regional Regulatory Affairs Manager in a timely manner. Advise Regional Regulatory Affairs Manager of upcoming renewals and commitments in a timely manner. Assist in the electronic submission of product dossiers, variations and responses to Proficient Authorities. Update and maintain product registration and ingredients archives, databases and tracking tools. Upload and publish electronic Common Technical Document (eCTD) sequences for medicinal products. Upload and maintain technical files/dossier databases for medical devices and biocides, also if required by the Regional RA team any documentation supporting the placing on the market of other categories of products eg cosmetics, home care, consumer goods Work closely with Global and European functions to obtain the relevant documents and information for product dossiers. Assist in the preparation of Regulatory Standard Operation Procedures, and in keeping track of revision dates. Handle the distribution lists of SOP and the archiving in the documentation system (DMS). Ensure accurate electronic archiving of all documents submitted to and received from Competent Authorities and Notified Bodies, as well as accurate and timely data updates of regulatory compliance databases and tools for assigned products. Assist the Regional Regulatory Affairs Managers in the review of list of ingredients for labeling purposes (eg. INCI and INDI). Assist the RA Managers with artwork review and approval Understand current regulations, guidelines and standards relevant to ensure compliance to the applicable regulatory and corporate standards/requirements (medicinal products, medical devices, cosmetic products, biocides, detergents, consumer goods). Ensure that the content, organization and overall quality of all regulatory documents are adequate and aligned with local/regional regulatory requirements, commitments and agreements. Supervise Proficient Authority websites and databases for news related to new product registrations and parallel imports from competition.   Qualification & Experience Bachelor’s degree in Pharmacy or Life Sciences or relevant education. Advanced degree preferred! Minimum 1 year of proven experience in regulatory affairs, quality or product development in pharmaceutical, medical devices or similar FMCG/CPG companies. Understanding of registration and regulatory requirements in European countries. Knowledge of industry practices, techniques and standards Knowledge and experience with medicinal products and medical devices is an advantage. Excellent digital literacy, which includes working with electronic databases, eCTD software, MS Office applications (working with templates, and editing and formatting sophisticated documents), Adobe Acrobat Standard or Professional, Internet and Intranet, Google Suite, SAP, DMS, and Authority Regulatory databases and portals for managing changes and submissions. Proficiency in spoken and written English. Knowledge of any additional language such as French or German is an advantage.  

  • pharma
  • Quality control
  • pharmacovigilance

Clinical Associate/Registrar

Manipal Hospitals

Full time
  • 0-1 years
  • Not Disclosed
  • Mangaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 0-1 years
  • Not Disclosed
  • Mangaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Qualification & Experience  DM/DNB Cardiology/DCH/MD/DNB Pediatrics /DM/Fellowship in PICU/Neonatology 0 to 10 years of experience  

  • clinical research
  • mbbs
  • MD

Duty Doctor

SCS Hospital

Full time
  • 0-1 years
  • Not Disclosed
  • Mangaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 0-1 years
  • Not Disclosed
  • Mangaluru, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Qualification & Experience Resident Medical Officer (RMO) for casualty Fresher or experienced - with MBBS qualification ( KMC Registration preferred). 1 year commitment preferred. Knowledge of English & local languages like Kannada is preferred  

  • mbbs
  • MD
  • Operations

Executive / Sr Executive- FRD Orals

Sun Pharmaceutical Industries Ltd.

Full time
  • 2+ years
  • Not Disclosed
  • Vadodara, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023
  • 2+ years
  • Not Disclosed
  • Vadodara, India
  • Post Date: Jan 23, 2023
  • End Date: Mar 23, 2023

Responsibilities As a Central Investigation Team member, primary role will be trending/statistical analysis/manufacturing process evaluation for the probable root cause and for other technical issues at manufacturing site. Assessment for Dissolution similarity as part of submission requirements. Statistical support for query response. Stability data analysis Other statistical analysis for content uniformity, probability of dissolution failures.   Experience 2 to 6 years  

  • Quality control
  • clinical research
  • pharmacovigilance

Research Associate / Senior Research Associate

Chemveda Life Sciences

Full time
  • 2+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Jan 31, 2023
  • 2+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Jan 31, 2023

Qualification & Experience M.sc (Organic Chemistry / Medicinal Chemistry) 2 to 10 years of experience  

  • Quality control
  • clinical research
  • pharmacovigilance

Research Associate / Senior Research Associate

Jubilant Biosys Limited

Full time
  • 1+ years
  • Not Disclosed
  • Noida, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 1+ years
  • Not Disclosed
  • Noida, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Expertise in : Lipids, Lipoids, long chain Lipids, multi-step synthesis of Lipids, non-UV active aliphatic compounds, aliphatic compounds.   Experience 1 to 8 years of experience  

  • Quality control
  • clinical research
  • pharmacovigilance

Business Development Manager

Lilac Insights

Full time
  • 2+ years
  • Not Disclosed
  • Thane, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 2+ years
  • Not Disclosed
  • Thane, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Locations: Thane, Aurangabad, Kolhapur   Qualification & Experience B Pharmacy / BSC / Biotechnology Min 2-4 years Sales experience in healthcare industry with Field work experience Preferably with Gynec Super-specialty.  

  • pharma
  • clinical research
  • product management

Executive/ Sr.Executive -Quality Assurance

Lee Pharma Limited

Full time
  • 1+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023
  • 1+ years
  • Not Disclosed
  • Hyderabad, India
  • Post Date: Jan 20, 2023
  • End Date: Mar 20, 2023

Responsibilities  Knowledge of Training, dispatches Audit works, All QA works   Qualification & Experience MSc / BSc With 1 to 5 Years of experience    

  • pharma
  • clinical research
  • product management

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