Labcorp Hiring Freshers as Investigator Support Assistant – Start Your Clinical Research Career!

Overview

If you’re a fresher looking to break into the clinical research industry, here’s your chance! Labcorp, a global leader in drug development and diagnostics, is hiring Investigator Support Assistants to strengthen its clinical research operations. This is an excellent opportunity to kickstart your career with one of the most reputed organizations in the healthcare sector.

Job Position & Details

Investigator Support Assistant

πŸ“Œ Department: Clinical Research
πŸ“Œ Qualification: Bachelor’s degree in Life Sciences, Pharmacy, or a related field
πŸ“Œ Experience: Freshers can apply!


πŸ“Œ Key Responsibilities:
βœ” Supporting investigators and study coordinators in clinical trials
βœ” Managing trial documentation and regulatory submissions
βœ” Ensuring compliance with study protocols and timelines
βœ” Coordinating site activities and communication with stakeholders
πŸ“Œ Salary: Competitive entry-level package
πŸ“Œ Location: Bangalore

Why Join Labcorp?

βœ… Work with a globally recognized CRO in clinical research
βœ… Hands-on experience in drug development processes
βœ… Learning & career growth opportunities in clinical trials
βœ… Competitive salary and supportive work culture

How to Apply?

Interested candidates can apply online through Labcorp’s official career portal. Ensure you have an updated resume and cover letter highlighting your interest in clinical research.

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RegDesk Hiring – Exciting Opportunity in Regulatory Intelligence!

Overview

πŸš€ Last Bench Pharmacist brings you an excellent opportunity at RegDesk, a leading provider of AI-powered regulatory solutions. The company is hiring Regulatory Intelligence Associates to support its global operations. If you have expertise in regulatory affairs and compliance, this is your chance to work with a cutting-edge organization!

Available Position

Regulatory Intelligence Associate

πŸ“Œ Department: Regulatory Affairs & Compliance
πŸ“Œ Qualification:
βœ” Bachelor’s/Master’s degree in Life Sciences, Pharmacy, Regulatory Affairs, or a related field
βœ” Candidates with certifications in regulatory affairs will have an advantage

πŸ“Œ Experience: 0-3 years in regulatory intelligence, compliance, or medical device/pharmaceutical regulations

πŸ“Œ Skills Required:
βœ” Strong knowledge of global regulatory guidelines (FDA, EMA, MHRA, TGA, etc.)
βœ” Experience in regulatory data analysis and documentation
βœ” Excellent research skills to track regulatory changes and requirements
βœ” Proficiency in regulatory submission processes

Job Responsibilities

πŸ”Ή Monitor global regulatory updates and changes in compliance requirements
πŸ”Ή Research and interpret regulatory laws, standards, and industry trends
πŸ”Ή Support the preparation and submission of regulatory documentation
πŸ”Ή Collaborate with cross-functional teams to ensure compliance with international regulations

Application Process

πŸ“© How to Apply: Interested candidates can send their resumes to careers@regdesk.com with the subject β€œApplication for Regulatory Intelligence Associate”

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Macleods Pharmaceuticals Hiring – Walk-in Interviews for Multiple Roles!

Overview

πŸš€ Last Bench Pharmacist brings you an excellent opportunity at Macleods Pharmaceuticals, one of India’s leading pharmaceutical companies. Macleods is conducting walk-in interviews for various roles in Production, Engineering, Quality Assurance (QA), and Quality Control (QC). If you are looking for a career in a reputed pharma company, this is your chance!

Available Positions & Details

1️⃣ Production – Manufacturing & Packing

πŸ“Œ Department: Tablet / Capsule / Injectable Manufacturing
πŸ“Œ Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc
πŸ“Œ Experience: 1-6 years in solid oral dosage / injectable manufacturing
πŸ“Œ Skills Required:
βœ” Expertise in Granulation, Compression, Coating, and Capsule Filling
βœ” Experience in Batch Manufacturing & Packing Operations
βœ” Knowledge of cGMP guidelines and SOPs

2️⃣ Quality Control (QC)

πŸ“Œ Department: Analytical Testing & Quality Control
πŸ“Œ Qualification: M.Sc / B.Pharm / M.Pharm
πŸ“Œ Experience: 1-5 years in pharma QC
πŸ“Œ Skills Required:
βœ” Hands-on experience in HPLC, GC, Dissolution, and Wet Analysis
βœ” Familiarity with pharmacopoeial standards (IP, BP, USP, EP)
βœ” Understanding of data integrity and regulatory guidelines

3️⃣ Quality Assurance (QA)

πŸ“Œ Department: Compliance & Documentation
πŸ“Œ Qualification: B.Pharm / M.Pharm / M.Sc
πŸ“Œ Experience: 1-6 years in QA Documentation & Validation
πŸ“Œ Skills Required:
βœ” Handling of Change Controls, Deviations, CAPA, and Risk Assessments
βœ” Experience in IPQA, Validation, and cGMP Compliance
βœ” Understanding of regulatory audits and documentation

4️⃣ Engineering

πŸ“Œ Department: Maintenance & Utility
πŸ“Œ Qualification: B.Tech / Diploma in Mechanical / Electrical / Instrumentation
πŸ“Œ Experience: 2-7 years in pharma plant engineering & maintenance
πŸ“Œ Skills Required:
βœ” Maintenance of HVAC, Water Systems, and Utilities
βœ” Experience with Plant Machinery & Equipment
βœ” Knowledge of calibration, validation, and safety protocols

Walk-in Interview Details

πŸ“… Date: 23rd & 24th February 2025
⏰ Time: 9:30 AM – 5:30 PM
πŸ“ Venue: Macleods Pharmaceuticals, [Exact Location Details]

Documents to Carry:

πŸ“Œ Updated Resume
πŸ“Œ Educational & Experience Certificates (Original & Photocopies)
πŸ“Œ Valid ID Proof
πŸ“Œ Passport-sized Photos

Can’t Attend the Walk-in?

πŸ“© Send Your Resume to: careers@macleodspharma.com with the subject β€œApplication for [Job Title]”

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RDTL Hiring Scientific Officers – Apply Now!

Overview

πŸš€ Last Bench Pharmacist brings you an exciting job opportunity at Regional Drug Testing Laboratory (RDTL). RDTL is hiring Scientific Officers for multiple positions, providing a great opportunity for professionals in pharmaceutical analysis and drug testing. If you’re looking to advance your career in a government-certified drug testing laboratory, this is your chance!

Available Positions & Details

1️⃣ Scientific Officer – Chemical Testing

πŸ“Œ Department: Drug Testing & Quality Control
πŸ“Œ Qualification: M.Sc in Chemistry / Pharmaceutical Chemistry / Analytical Chemistry
πŸ“Œ Experience: 2-5 years in pharma analysis / QC laboratories
πŸ“Œ Skills Required:
βœ” Expertise in HPLC, GC, UV-Vis Spectroscopy, and FTIR
βœ” Hands-on experience with analytical method development & validation
βœ” Knowledge of pharmacopoeial standards (IP, BP, USP, EP)
πŸ“Œ Salary: Competitive, based on experience
πŸ“Œ Location: Regional Drug Testing Laboratory (RDTL)

2️⃣ Scientific Officer – Microbiology

πŸ“Œ Department: Microbial Testing & Quality Control
πŸ“Œ Qualification: M.Sc in Microbiology / Biotechnology
πŸ“Œ Experience: 1-3 years in pharmaceutical microbiology testing
πŸ“Œ Skills Required:
βœ” Expertise in sterility testing, microbial identification, and endotoxin testing
βœ” Knowledge of pharmacopoeial microbiological standards
βœ” Experience in media preparation, culture maintenance, and validation
πŸ“Œ Salary: Competitive, based on experience
πŸ“Œ Location: Regional Drug Testing Laboratory (RDTL)

How to Apply?

βœ… Walk-in Interview Date: πŸ“… 26th & 27th February 2025
βœ… Time: ⏰ 9:30 AM – 5:30 PM
βœ… Venue: πŸ“ Regional Drug Testing Laboratory (RDTL),

Documents to Carry:

πŸ“Œ Updated Resume
πŸ“Œ Educational & Experience Certificates (Original & Photocopies)
πŸ“Œ Valid ID Proof
πŸ“Œ Passport-sized Photos

Can’t Attend the Walk-in?

πŸ“© Send Your Resume to: careers@rdtl.gov.in with the subject β€œApplication for [Job Title]”

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Cadila Pharmaceuticals Hiring Freshers & Experienced for Biotech & Vaccine Upstream –

Overview

πŸš€ Last Bench Pharmacist brings you another exciting pharma job opportunity! Cadila Pharmaceuticals is hiring both freshers and experienced professionals for multiple roles in Biotech & Vaccine Upstream Processing. If you’re looking to start or advance your career in biotechnology and vaccine manufacturing, this is the perfect opportunity to join a leading pharmaceutical company.

Available Positions & Details

1️⃣ Executive / Sr. Executive – Upstream Processing

πŸ“Œ Department: Biotechnology / Vaccine Manufacturing
πŸ“Œ Qualification: M.Sc / B.Tech / M.Tech in Biotechnology / Microbiology / Biochemistry
πŸ“Œ Experience: 2-6 years
πŸ“Œ Skills Required:
βœ” Hands-on experience in bioreactors (single-use & stainless steel)
βœ” Expertise in cell culture, microbial fermentation, and media preparation
βœ” Understanding of GMP compliance and regulatory guidelines
πŸ“Œ Location: Dholka, Gujarat

2️⃣ Officer / Executive – Vaccine Production (Freshers & Experienced)

πŸ“Œ Department: Vaccine Upstream Processing
πŸ“Œ Qualification: B.Sc / M.Sc / B.Tech / M.Tech in Biotechnology, Microbiology, or Biochemistry
πŸ“Œ Experience: 0-3 years (Freshers can apply)
πŸ“Œ Skills Required:
βœ” Exposure to cell culture, fermentation, and media preparation
βœ” Basic knowledge of bioprocess engineering and aseptic techniques
βœ” Willingness to work in a cGMP-compliant environment
πŸ“Œ Location: Dholka, Gujarat

How to Apply?

βœ… Walk-in Interview Date: πŸ“… 24th & 25th February 2025
βœ… Time: ⏰ 9:30 AM – 5:30 PM
βœ… Venue: πŸ“ Cadila Pharmaceuticals, Dholka, Gujarat

Documents to Carry:

πŸ“Œ Updated Resume
πŸ“Œ Educational & Experience Certificates (Original & Photocopies)
πŸ“Œ Valid ID Proof
πŸ“Œ Passport-sized Photos

Can’t Attend the Walk-in?

πŸ“© Send Your Resume to: careers@cadilapharma.com with the subject β€œApplication for [Job Title]”

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Exciting Career Openings at Novotech – Join the Pharmacovigilance & DSA Team!

Overview

Last Bench Pharmacist brings another excellent opportunity for professionals looking to advance their careers in clinical research! Novotech, a leading global contract research organization (CRO), is hiring for Pharmacovigilance and DSA (Drug Safety Associate) roles. If you have a passion for ensuring drug safety and regulatory compliance, this could be your next big career move.

Open Positions & Details

1. Drug Safety Associate (DSA)

πŸ“Œ Department: Pharmacovigilance
πŸ“Œ Qualification: Bachelor’s or Master’s in Life Sciences, Pharmacy, or a related field
πŸ“Œ Experience: 1-3 years in pharmacovigilance or drug safety
πŸ“Œ Key Skills:
βœ” Case processing and medical coding
βœ” Signal detection and safety reporting
βœ” Adverse event management and regulatory compliance
πŸ“Œ Salary: Competitive package based on experience
πŸ“Œ Location: Multiple locations

2. Pharmacovigilance Specialist

πŸ“Œ Department: Drug Safety & Risk Management
πŸ“Œ Qualification: PharmD, MSc, or relevant degree in Life Sciences
πŸ“Œ Experience: 3+ years in pharmacovigilance and clinical research


πŸ“Œ Key Skills:
βœ” Risk assessment and benefit-risk evaluation
βœ” Literature screening and aggregate report writing
βœ” Hands-on experience with PV databases
πŸ“Œ Salary: β‚Ή6-10 LPA (Based on skills & experience)
πŸ“Œ Location: Bangalore / Hyderabad

Why Join Novotech?

βœ… Work with a globally recognized CRO
βœ… Opportunity to collaborate with international clients
βœ… Cutting-edge technology and research exposure
βœ… Competitive salary and career growth opportunities

Walk-in Interview Details

πŸ“ Venue: Novotech India Pvt. Ltd., Bangalore
πŸ“… Date: 1st & 2nd March 2025
⏰ Time: 9:30 AM – 4:30 PM

Documents to Carry

βœ” Updated Resume
βœ” Educational & Experience Certificates (Original & Photocopies)
βœ” Government ID Proof
βœ” Passport-sized Photos

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For more job openings, visit Last Bench Pharmacist regularly. πŸš€

THSTI Hiring for Multiple Research Positions – Walk-in Interviews

Overview

Last Bench Pharmacist brings you an exciting opportunity at Translational Health Science and Technology Institute (THSTI), a premier institute under the Department of Biotechnology, Government of India. THSTI is actively hiring for multiple research positions in Life Sciences, Virology, and Clinical Research. If you are looking to build a career in translational research, this is your chance to join a leading research institute.

Available Positions & Details

1. Research Associate-I

πŸ“Œ Project: Development of highly infectious BSL4 viral agent’s pseudo viruses and its applicability to facilitate research of highly pathogenic and emerging zoonotic viruses.
πŸ“Œ Principal Investigator: Dr. Sweety Samal
πŸ“Œ Qualification: PhD in Life Sciences from a recognized university.
πŸ“Œ Desirable: First-author publication in a reputed journal.
πŸ“Œ Experience & Skills:
βœ” Virology, cell culture, and immunological assays.
βœ” Handling live viruses & performing neutralization assays.
βœ” Molecular biology techniques & animal handling.
βœ” Protein purification (FPLC/HPLC), flow cytometry, and confocal microscopy.


πŸ“Œ Salary: β‚Ή58,000 + HRA
πŸ“Œ Age Limit: 35 years
πŸ“Œ Walk-in Interview Date: 3rd March 2025

2. Project Associate-II

πŸ“Œ Project: Targeting Two Component Signaling Systems (TCSs) in M. Tuberculosis to counteract adaptation of tubercle bacilli.
πŸ“Œ Principal Investigator: Dr. Ramandeep Singh
πŸ“Œ Qualification: Master’s degree in Life Sciences with 2+ years of research experience.
πŸ“Œ Experience & Skills:
βœ” DNA cloning, protein purification, and western blotting.
βœ” Flow cytometry (FACS) and microbiology techniques.
βœ” Animal handling experience.
πŸ“Œ Salary:

  • β‚Ή35,000 + HRA (With NET/GATE)
  • β‚Ή28,000 + HRA (Without NET/GATE)
    πŸ“Œ Age Limit: 35 years
    πŸ“Œ Walk-in Interview Date: 25th February 2025

3. Senior Project Associate

πŸ“Œ Project: Inter-Institutional Program for Maternal, Neonatal, and Infant Sciences – GARBHINI Phase-II
πŸ“Œ Principal Investigators: Dr. Shinjini Bhatnagar & Dr. Nitya Wadhwa
πŸ“Œ Qualification:
βœ” Master’s in Life Sciences/Agriculture/Veterinary Sciences with 4+ years of research experience.
βœ” OR PhD in Science/Engineering/Pharma.


πŸ“Œ Experience & Skills:
βœ” Overseeing clinical trials and ensuring compliance with GCP & regulatory requirements.
βœ” Conducting site monitoring, quality assurance, and training activities.
βœ” Managing trial documentation and ensuring data integrity.
πŸ“Œ Salary: β‚Ή42,000 + HRA
πŸ“Œ Age Limit: 40 years
πŸ“Œ Walk-in Interview Date: 28th February 2025

How to Apply?

βœ… Attend the walk-in interviews on the specified dates.
βœ… Documents to Carry:
πŸ“Œ Updated Resume
πŸ“Œ Educational & Experience Certificates (Original & Photocopies)
πŸ“Œ Valid ID Proof
πŸ“Œ Passport-sized Photos

πŸ“ Venue:
THSTI, NCR Biotech Science Cluster,
3rd Milestone, Faridabad-Gurugram Expressway, Faridabad

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Join our WhatsApp Channel to get daily pharma job updates. πŸ“²Click Here to Join

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Clinspire Hiring Clinical Research Coordinators

Overview

Last Bench Pharmacist brings you an exciting job opportunity at Clinspire, a leading clinical research organization. They are hiring Clinical Research Coordinators in Patna, Varanasi, and Prayagraj. If you have a background in Life Sciences or Pharmacy and are eager to start your career in clinical research, this is your chance!

Job Details

πŸ“Œ Role: Clinical Research Coordinator
πŸ“Œ Job Locations & Vacancies:

  • Patna: 2 Vacancies
  • Varanasi: 3 Vacancies
  • Prayagraj: 1 Vacancy

πŸ“Œ Qualifications Required:
βœ” B.Sc. (Life Sciences)
βœ” M.Sc. (Life Sciences)
βœ” B. Pharm

πŸ“Œ Experience: 0-1 year (Freshers are encouraged to apply!)
πŸ“Œ Preferred Candidates: Local or nearby applicants for easy commuting.

Key Responsibilities

πŸ”Ή Assist in planning and executing clinical trials.
πŸ”Ή Coordinate with regulatory authorities, investigators, and participants.
πŸ”Ή Ensure compliance with study protocols and regulatory guidelines.
πŸ”Ή Maintain accurate and timely documentation.
πŸ”Ή Support data management and integrity in clinical research studies.

Why Join Clinspire?

βœ… Career Growth: Gain hands-on experience and advance in clinical research.
βœ… Innovative Work Culture: Work in a dynamic and collaborative team.
βœ… Impactful Research: Contribute to studies that improve healthcare.

How to Apply?

πŸ“§ Interested candidates should send their CVs to contact@clinspire.in.

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BioRadius Therapeutic Research Hiring – Walk-In for Multiple Clinical Research Roles

Overview
Last Bench Pharmacist brings you an exciting job opportunity at BioRadius Therapeutic Research, a leading Contract Research Organization (CRO) based in Pune, India. With a strong track record of successful USFDA regulatory audits and UK MHRA product approvals, BioRadius is expanding its team and looking for talented professionals to join them. If you are looking for a rewarding career in clinical research, this is your chance!

Job Openings at BioRadius Therapeutic Research
1. Clinical Research Associates (0-2 Years Experience)
πŸ“Œ Experience Level: Freshers or candidates with up to 2 years of experience
πŸ“Œ Qualification: B. Pharma or Life Sciences graduates
πŸ“Œ Role Overview: Responsible for managing clinical trials, ensuring compliance with protocols, and collecting essential data for groundbreaking research.
πŸ“Œ Who Should Apply? Freshers and experienced candidates eager to start their career in clinical research.

2. Clinical QA Executives (4-6 Years Experience)
πŸ“Œ Experience Level: 4-6 years in quality assurance or related fields
πŸ“Œ Role Overview: Ensure compliance with stringent regulatory standards and maintain the integrity of research activities.
πŸ“Œ Who Should Apply? Experienced professionals looking for a leadership role in a fast-paced clinical research environment.

3. Bioanalytical Team Lead (LCMS/MS) (5-8 Years Experience)
πŸ“Œ Experience Level: 5-8 years with expertise in LCMS/MS (Liquid Chromatography-Mass Spectrometry)
πŸ“Œ Role Overview: Oversee bioanalytical studies, manage research teams, and contribute to pharmaceutical advancements using LCMS/MS technology.
πŸ“Œ Who Should Apply? Seasoned professionals with a strong background in bioanalytical studies.

Walk-In Interview Details
πŸ“… Date: February 24–28, 2025
⏰ Time: 11:00 AM to 1:00 PM
πŸ“ Venue: BioRadius Therapeutic Research, Plot No. 8, Indialand Global Industrial Park, Hinjawadi Phase-I, Pune 411057
πŸ“ž Contact: Text 8080104848 (No calls, only messages)

Documents to Carry
βœ” Updated Resume
βœ” Educational Certificates (Degree & Mark Sheets)
βœ” Latest Increment Letter (if applicable)
βœ” Last 3 months’ pay slips
βœ” Last 6 months’ bank statements
βœ” 2 Passport-sized photos
βœ” Aadhar Card Copy

Why Join BioRadius Therapeutic Research?
🌟 Work with an Industry Leader: BioRadius has received multiple USFDA and UK MHRA approvals, ensuring global recognition.
πŸ“ˆ Career Growth: Be part of a company that is expanding and aiming to lead the CRO industry.
πŸ”¬ Cutting-Edge Research: Work on innovative pharmaceutical and biopharmaceutical research projects.
πŸ‘¨β€πŸ”¬ Expert Team: Collaborate with experienced professionals in the clinical research industry.

Who Can Apply?
βœ… Freshers and experienced candidates with clinical research or bioanalytical backgrounds.
βœ… Professionals with expertise in QA, LCMS/MS, and clinical trial management.
βœ… Those looking for a challenging and rewarding career in a globally recognized CRO.

πŸ“’ Stay Updated!
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AIIMS New Delhi – Hiring Clinical Research Coordinator


Overview
Last Bench Pharmacist brings you an exciting job opportunity at the All India Institute of Medical Sciences (AIIMS), New Delhi. The Department of Pulmonary, Critical Care, and Sleep Medicine is recruiting for the position of Clinical Research Coordinator for a prestigious project focusing on chronic obstructive pulmonary disease (COPD) research.
This is a golden opportunity for candidates passionate about clinical research to work in a world-class medical institution.

Job Details
πŸ“Œ Post: Clinical Research Coordinator
πŸ“Œ Number of Positions: 1
πŸ“Œ Duration: 3 years
πŸ“Œ Salary: β‚Ή30,000 per month
πŸ“Œ Age Limit: 35 years (Age relaxation: 5 years for SC/ST, 3 years for OBC candidates)
πŸ“Œ Project Name: THARROS – A Phase III Study on Cardiopulmonary Outcomes in COPD

Eligibility Criteria
βœ” Bachelor’s Degree in a relevant subject with 2 years of experience in a related field.
βœ” Master’s Degree in a relevant field (preferred but not mandatory).
βœ” Experience in clinical research, particularly in pulmonary or critical care studies, will be an added advantage.

Key Responsibilities
πŸ”Ή Assist in coordinating clinical research activities.
πŸ”Ή Ensure compliance with regulatory guidelines.
πŸ”Ή Collect and analyze clinical data.
πŸ”Ή Support the research team in patient monitoring and documentation.

How to Apply?
πŸ“§ Interested candidates must email their resume to pulmonaryproject2021@gmail.com by 25th February 2024, 5 PM.
πŸ“ Important Note: Mention β€œApplication for Clinical Research Coordinator” in the email subject line. Applications without the correct subject line will NOT be considered.

Why Join AIIMS New Delhi?
βœ… Prestigious Institution – Work with one of India’s top medical research institutes.
βœ… Cutting-Edge Research – Be part of a significant clinical trial on COPD treatment.
βœ… Career Growth – Gain valuable experience in the field of clinical research.

updates.
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