trials Jobs

Parexel is currently seeking a Clinical Programmer to join us in South Africa, dedicated to a single sponsor. This role will be responsible for the provision of da...

Company GFCL EV Products Limited Grade / Level N/A Division / Department Technical Services Job Purpose Assist for process/project engineering and Front end engineering and project implementat...
Technology transferScale upTechnical services

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

A Pharmacovigilance Officer is responsible for monitoring and assessing the safety of marketed drugs by collecting, analyzing, and reporting adverse drug reactions (ADRs) from patients and healt...
clinical researchpharmacologydrug monitoringdrug safetyclinical monitoringadverse event reportingtrialsclinical pharmacology

Regulatory Affairs Officer: A regulatory specialist is responsible for ensuring a company adheres to all applicable laws, regulations, and standards within their industry by re...
clinical researchclinical research associatesclinical monitoringtrialsclinical pharmacologyclinical data management

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

A Pharmacovigilance Officer is responsible for monitoring and assessing the safety of marketed drugs by collecting, analyzing, and reporting adverse drug reactions (ADRs) from patients and healt...
clinical researchpharmacologydrug monitoringdrug safetyclinical monitoringadverse event reportingtrialsclinical pharmacology

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

A Pharmacovigilance Officer is responsible for monitoring and assessing the safety of marketed drugs by collecting, analyzing, and reporting adverse drug reactions (ADRs) from patients and healt...
clinical researchpharmacologydrug monitoringdrug safetyclinical monitoringadverse event reportingtrialsclinical pharmacology

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

Regulatory Affairs Officer: A regulatory specialist is responsible for ensuring a company adheres to all applicable laws, regulations, and standards within their industry by re...
clinical researchclinical research associatesclinical monitoringtrialsclinical pharmacologyclinical data management

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

A Pharmacovigilance Officer is responsible for monitoring and assessing the safety of marketed drugs by collecting, analyzing, and reporting adverse drug reactions (ADRs) from patients and healt...
clinical researchpharmacologydrug monitoringdrug safetyclinical monitoringadverse event reportingtrialsclinical pharmacology

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

A Pharmacovigilance Officer is responsible for monitoring and assessing the safety of marketed drugs by collecting, analyzing, and reporting adverse drug reactions (ADRs) from patients and healt...
clinical researchpharmacologydrug monitoringdrug safetyclinical monitoringadverse event reportingtrialsclinical pharmacology

A clinical database programmer is responsible for designing, developing, and maintaining databases used to store and manage clinical trial data, including patient information, study outcomes, and ...
clinical researchdata collectiondata analysiselectronic data captureclinical trials

A Pharmacovigilance Officer is responsible for monitoring and assessing the safety of marketed drugs by collecting, analyzing, and reporting adverse drug reactions (ADRs) from patients and healt...
clinical researchpharmacologydrug monitoringdrug safetyclinical monitoringadverse event reportingtrialsclinical pharmacology

Regulatory Affairs Officer: A regulatory specialist is responsible for ensuring a company adheres to all applicable laws, regulations, and standards within their industry by re...
clinical researchclinical research associatesclinical monitoringtrialsclinical pharmacologyclinical data management

As a clinical research associate (CRA), youll run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use. Youll work on new a...
pharmacypharmabiotechnology

As a clinical research associate (CRA), youll run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use. Youll work on new a...
pharmacypharmabiotechnology

As a clinical research associate (CRA), youll run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use. Youll work on new a...
pharmacypharmabiotechnology

Company:Intas Pharma Job Description-Medical Advisor- Ahmedabad The Medical Advisor will provide scientific and clinical experti...
communicationdevelopmentstrategykolclinicalengagementmedicaladvisor

Roles and Responsibilities

• Developing growth strategies and plans
• Managing and retaining relationships with existing clients and increasing client ...
  market penetration zoho sales sales executive business proposals sales management negotiation business development executive industry knowledgebusiness management marketing activities marketing

A clinical data quality manager is primarily responsible for ensuring the accuracy, completeness, and integrity of clinical trial data by overseeing data collection processes, reviewing case repor...
clinical researchelectronic data captureclinical trials

A Regulatory Affairs Manager is primarily responsible for ensuring a companys products comply with all relevant local and international regulations by developing and implementing strategies to n...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

A clinical data quality manager is primarily responsible for ensuring the accuracy, completeness, and integrity of clinical trial data by overseeing data collection processes, reviewing case repor...
clinical researchelectronic data captureclinical trials

A drug safety manager, also known as a pharmacovigilance manager, is primarily responsible for overseeing all aspects of drug safety within a pharmaceutical company, including monitoring adverse...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

A clinical data quality manager is primarily responsible for ensuring the accuracy, completeness, and integrity of clinical trial data by overseeing data collection processes, reviewing case repor...
clinical researchelectronic data captureclinical trials

A Regulatory Affairs Manager is primarily responsible for ensuring a companys products comply with all relevant local and international regulations by developing and implementing strategies to n...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

A Drug Safety Physician or Medical Reviewer is a medical professional who is responsible for evaluating and assessing the safety and efficacy of drugs, both before and after they are approved for...
safetyargusclinical trial management systemclinicalculturetrialshealthsafety administrationdatadrug

Job Title: Clinical SAS Programmer / Developer with Power BI Location: Mumbai, Chennai, Pune, Hyderabad Experience: 5 to 10 Years Notice Period: Immediate to 15 Days We are looking for an exp...
sdtmpower bistatistical programmingadamcdisc standardstlf

A clinical data quality manager is primarily responsible for ensuring the accuracy, completeness, and integrity of clinical trial data by overseeing data collection processes, reviewing case repor...
clinical researchelectronic data captureclinical trials

A drug safety manager, also known as a pharmacovigilance manager, is primarily responsible for overseeing all aspects of drug safety within a pharmaceutical company, including monitoring adverse...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

A Drug Safety Physician or Medical Reviewer is a medical professional who is responsible for evaluating and assessing the safety and efficacy of drugs, both before and after they are approved for...
safetyargusclinical trial management systemclinicalculturetrialshealthsafety administrationdatadrug

Job Title: Clinical SAS Programmer / Developer with Power BI Location: Mumbai, Chennai, Pune, Hyderabad Experience: 5 to 10 Years Notice Period: Immediate to 15 Days We are looking for an exp...
sdtmpower bistatistical programmingadamcdisc standardstlf

A clinical data quality manager is primarily responsible for ensuring the accuracy, completeness, and integrity of clinical trial data by overseeing data collection processes, reviewing case repor...
clinical researchelectronic data captureclinical trials

A Regulatory Affairs Manager is primarily responsible for ensuring a companys products comply with all relevant local and international regulations by developing and implementing strategies to n...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

A drug safety manager, also known as a pharmacovigilance manager, is primarily responsible for overseeing all aspects of drug safety within a pharmaceutical company, including monitoring adverse...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

A clinical data quality manager is primarily responsible for ensuring the accuracy, completeness, and integrity of clinical trial data by overseeing data collection processes, reviewing case repor...
clinical researchelectronic data captureclinical trials

A Regulatory Affairs Manager is primarily responsible for ensuring a companys products comply with all relevant local and international regulations by developing and implementing strategies to n...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

A drug safety manager, also known as a pharmacovigilance manager, is primarily responsible for overseeing all aspects of drug safety within a pharmaceutical company, including monitoring adverse...
clinical monitoringclinical researchclinicaltrialsclinical research associatesclinical data management

As a medical writer, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our organization. You will cover topics in clinical trials, treatments, ...
healthcarebillingpatient assessmentcoding

Job Title: Agriculture Engineer (Food Technology) Agri Dryer Department Location: Kothamangalam Job Type: Full-time Experience Level: Freshers & Experienced Candidates Welcome Salary: 15,000 (neg...
Analytical SkillsCommunication SkillsTeamworkProblemsolving SkillsKnowledge of Industry RegulationsFood Drying TechniquesPostharvest ProcessingFood Preservation MethodsDrying Equipment

Job Title: Technical Marketing Executive Textile Chemicals Location: Surat Position Overview: We are looking for a Technical Marketing Executive with a background in textile processing to driv...
communicationnegotiationtechnical knowledge of textile processingchemicalsexplain technical concepts effectivelytravel extensively for client meetings

You will be required to manage the data collected during trials, oversee trial sites, and conduct regular site visits to monitor the progress. You will also collaborate with the sponsors at trial...
healthcarepatient carecodingbilling

Job Profile: Ayurveda R&D Specialist Jivada Ventures Pvt Ltd Job Overview: The Ayurveda R&D Specialist at Jivada Ventures Pvt Ltd will be responsible for researching, developing, and innovating...
AyurvedaDermatologyNeurologyPhytochemistrySustainabilityRasayana therapyInflammation biologyHerbal formulationNatural preservativesInterpreting scientific researchClinical trial data analysisClean beauty

As a medical writer, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our organization. You will cover topics in clinical trials, treatments, ...
healthcarebillingpatient assessmentcoding

As a medical writer, you will be responsible for writing documents, articles, journals, brochures, and product manuals for our organization. You will cover topics in clinical trials, treatments, ...
healthcarebillingpatient assessmentcoding

Company. Site Management Organization Role Description This is a full-time on-site role for a Clinical Research Coordinator at Pacific Clinical Research Services located in Jodhpur. The CRC will...
Data CollectionDocumentationRegulatory ComplianceClinical Research CoordinationStudy Protocol ManagementAttention to Detail