Executive

0-5 years

Preffered by Company

India

10 Aug. 29, 2024

Job Description

Job Type: Full Time Education: B.Pharm/ M.Pharm/ B.Sc/ M.Sc/ Any LifeScience Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Responsibilities:

Study Plan and SOP Compliance:
- Access and adhere to the Study Plan and Standard Operating Procedures (SOPs).
- Follow all instructions detailed in the Study Plan and SOPs to ensure compliance.
Data Recording and Quality:
- Record raw data promptly and accurately, adhering to the Principles of Good Laboratory Practice (GLP).
- Review raw data to ensure quality and accuracy, taking responsibility for data integrity.
Instrumentation Operation and Maintenance:
- Operate, maintain, and calibrate Liquid Chromatography and Tandem Mass Spectrometry (LC/MS/MS) equipment.
Method Development and Validation:
- Perform method development, method validation, and study sample analysis (non-clinical) in accordance with GLP guidelines.
Documentation and SOP Preparation:
- Prepare Analytical Test Procedures (ATPs), SOPs, and templates for GLP studies.
- Maintain and calibrate pipettes as assigned to the group.
Sample Preparation:
- Prepare samples for method development (MD), method validation (MV), and study analysis following GLP guidelines.
Reporting and Documentation:
- Draft method validation or partial method validation reports and bioanalytical study reports in consultation with the Study Director or Principal Investigator, ensuring compliance with GLP principles.
- Document and communicate any deviations in the GLP study report directly to the Study Director or Principal Investigator as appropriate.
- Address and respond to Quality Assurance (QA) observations on bioanalytical reports in consultation with the Study Director or Principal Investigator, maintaining adherence to GLP principles.
Additional Responsibilities:
- Undertake any other tasks or responsibilities assigned by the reporting authority.

Latest Jobs

Pharma Jobs in India

Andra Pradesh :

Assam :

Dibrugarh | Diburghar | Guwahati |

Bihar :

Hajipur | Patna |

Chhattisgarh :

Bilaspur | Raipur |

Delhi :

Delhi | India | New Delhi | PAN-India |

Goa :

Goa | Panaji |

Gujarat :

Haryana :

Himachal Pradesh :

Solan |

Jharkhand :

Ranchi |

Karnataka :

Kerala :

Kannur | Kochi | Malappuram | Thiruvananthapuram |

Madhya Pradesh :

Maharashtra :

PAN-India :

Panjab :

Punjab :

Rajasthan :

Banasthali | Jaipur | Pilani | Udaipur |

Tamil Nadu :

Uttar Pradesh :

Uttarakhand :

Dehradun | Nainital | Rishikesh |

West Bengal :

Kolkata | Mukundapur |

Pharma Jobs in United States

Alabama :

Birmingham |

Alaska :

Arizona :

California :

Colorado :

Denver |

Connecticut :

Groton | Storrs |

D.C :

Washington |

Florida :

Georgia :

Atlanta |

Hawaii :

Honolulu |

Illinois :

Indiana :

Bloomington | West Lafayette |

Kansas :

Lawrence |

LA :

Monroe | New Orleans |

Maryland :

Baltimore | Elkridge | Gaithersburg | Rockville |

Massachusetts :

Michigan :

Detroit |

Minnesota :

Minneapolis and St. Paul, Minnesota. |

Missouri :

Fulton | St. Louis |

New Jersey :

New York :

North Carolina :

Concord |

North Caroline :

Ohio :

Cincinnati | Cleveland | Columbus, |

Oregon :

Pennsylvania :

Portugal :

Lisbon |

Puerto Rico :

San Juan |

Republic of Mexico :

Mexico |

Tennessee :

Nashville |

Texas :

Austin | Dallas | Houston | Richardson |

Virginia :

Blacksburg | Charlottesville | Falls Church |

Washington :

Goldendale | Pullman | Seattle |

WI :

Madison | Wausau |

Wisconsin :

Wyoming :

Cokeville |

Pharma Jobs in Germany

Baden-Wurttemberg :

Bavaria :

Berlin :

Mitte |

Brandenburg :

Berlin |

Germany :

Germany | GErmany |

Hesse :

Marburg |

Hessen :

Frankfurt |

Lower Saxony :

Gottingen | Hannover | Leipzig |

Mecklenburg Vorpommern :

Rostock |

Munich :

Bavaria |

North Rhine Westphalia :

Rhineland Palatinate :

Mainz |

Rotherbaum :

Hamburg |

Saarland :

Saarbrucken |

Saxony Anhalt :

Halle |

Schleswig Holstein :

Kiel |

Pharma Jobs in Europe

Denmark :

Copenhagen |

Hungary :

Budapest |

Istanbul :

Turkey |

Romania :

Romania |

Serbia :

Belgrade |

Switzerland :

Basel | Zurich |

Pharma Jobs in China

Hubei :

Wuhan |

Republic of China :

Beijing |

Shanghai Sai :

Shanghai Shi |

Tokiyo :

Osaka | Tokyo |

Pharma Jobs in Argentina & Australia & Canada & Colombia & Croatia & Egypt & England & Indonesia & Ireland & Israel & Japan & Korea & Netherland & Remote & Saudi Arabia & Spain & Thailand

Buenos Aires :

Buenos Aires |

New South Wales :

Sydney |

Queensland :

Queensland |

Republic of Western Australia :

Nedlands |

Ontario :

North York | Richmond Hill |

Quebec :

Montreal |

Republic of Colombia :

Bogota |

Zagreb :

Zagreb |

Republic of Egypt :

Cairo |

United Kingdom :

London | Harlow | Salt Lake City |

Jakarta :

Jakarta |

County Dublin :

Swords |

Republic of Ireland :

Limerick | Waterford | Dublin |

Israel :

Kfar Saba | Be'Er Sheva | Netanya | Tel Aviv |

Tokyo :

Otemachi |

Republic of Korea :

Seoul |

Capital of Netherland :

Amsterdam |

Noord Holland :

Haarlem |

Remote :

Remote - Europe | Remote | Switzerland | Remote, USA |

Makkah :

Catalonia :

Barcelona |

Republic of Thailand :

Bangkok |

Executive

Job Description

Responsibilities:

Latest Jobs

Regulatory & Start Up Specialist I, Us Support, Cfsp

Fsp - Sr. Regulatory & Start Up Specialist

Assoc Manager, Regulatory & Start Up (Fsp)

Regulatory And Start Up Specialist - Romania

Regulatory & Start Up Specialist, Cfsp

Manager, Regulatory And Start-Up

Regulatory Affairs Global Labeling Lead

Sr. Specialist, Global Medical Affairs (Hst)