Job Summary: We are seeking a highly skilled and detail-oriented Medical Writer to join our dynamic team. The ideal candidate will have expertise in writing, editing, and reviewing scientific and medical content. The Medical Writer will be responsible for transforming complex medical data and research findings into clear, accurate, and engaging documents for various audiences, including healthcare professionals, regulatory bodies, and the general public. Key Responsibilities: Scientific and Medical Writing: Develop, write, and edit a wide range of documents including clinical study reports, regulatory submission documents (e.g., IND, NDA), peer-reviewed publications, and educational materials. Content Creation: Generate high-quality manuscripts, abstracts, posters, and presentations for scientific conferences, journals, and other outlets. Collaboration: Work closely with researchers, clinicians, regulatory affairs, and other stakeholders to ensure that all content meets regulatory standards, scientific accuracy, and corporate goals. Regulatory Submissions: Prepare and revise documents required for regulatory submissions, ensuring compliance with relevant guidelines (FDA, EMA, ICH). Literature Review & Research: Conduct literature searches and review existing medical research to support content development, ensuring accurate and up-to-date information. Quality Assurance: Edit and proofread content for clarity, consistency, accuracy, grammar, and adherence to style guides. Project Management: Manage timelines for multiple projects, ensuring timely and efficient completion of tasks. Compliance: Ensure all written materials are in compliance with medical, ethical, and regulatory standards. Qualifications: Education: Bachelor’s degree in Life Sciences, Medicine, Pharmacy, or a related field. A Master’s degree or PhD is a plus. Experience: Minimum of 2 years of experience in medical writing, clinical research, or a related field. Experience with regulatory documents is highly preferred. Knowledge: Strong understanding of clinical research, medical terminology, and regulatory guidelines. Technical Skills: Proficiency with Microsoft Office Suite, reference management software (e.g., EndNote, RefWorks), and familiarity with medical writing software (e.g., Manuscript Manager, LaTeX). Communication Skills: Excellent written and verbal communication skills, with the ability to convey complex information clearly and concisely. Attention to Detail: Strong attention to detail with a focus on accuracy and quality. Collaboration: Ability to work independently and as part of a team in a fast-paced environment. Language Proficiency: Exceptional command of the English language. Knowledge of additional languages is a plus. Desirable Skills: Experience with writing for regulatory agencies (FDA, EMA, etc.). Familiarity with scientific publishing and journal submission processes. Knowledge of Good Clinical Practice (GCP) and other relevant regulations. Experience with statistical analysis and interpretation of clinical data. Job Types: Full-time, Permanent Pay: From ₹25,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Fixed shift Work Location: In person
Job Summary: We are looking for an experienced and proactive Project Coordinator to join our Clinical Research Department. The ideal candidate will have 5–6 years of relevant experience in coordinating clinical research projects, ensuring they are executed efficiently, within timelines, and in compliance with regulatory and organizational standards Key Responsibilities: 1. Study Coordination: Manage daily activities of clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements. 2. Site Management: Develop and maintain relationships with study sites, investigators, and staff. 3. Regulatory Compliance: Ensure compliance with regulatory requirements, including IRB/IEC submissions and approvals. 4. Data Management: Oversee data collection, management, and quality control. 5. Communication: Facilitate communication among study sites, sponsors, and other stakeholders. 6. Problem-Solving: Identify and resolve issues that arise during the study. 7. Documentation: Maintain accurate and complete study documentation. Requirements: 1. Education: Bachelor's degree in a life science, nursing, or related field. 2. Experience: 5 to 6 experience in clinical research coordination. 3. Skills: Strong organizational, communication, and problem-solving skills. 4. Knowledge: Familiarity with GCP, regulatory requirements, and clinical trial operations. Desirable Skills: 1. Certification: Certification in clinical research coordination (e.g., CCRA or CCRC). 2. Experience with Clinical Trial Management Systems (CTMS): Familiarity with CTMS and electronic data capture (EDC) systems. Job Types: Full-time, Permanent Pay: ₹45,000.00 - ₹50,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Fixed shift Work Location: In person Application Deadline: 20/07/2025
Job Summary: We are looking for an experienced and proactive Project Coordinator to join our Clinical Research Department. The ideal candidate will have 5–6 years of relevant experience in coordinating clinical research projects, ensuring they are executed efficiently, within timelines, and in compliance with regulatory and organizational standards Key Responsibilities: 1. Study Coordination: Manage daily activities of clinical trials, ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements. 2. Site Management: Develop and maintain relationships with study sites, investigators, and staff. 3. Regulatory Compliance: Ensure compliance with regulatory requirements, including IRB/IEC submissions and approvals. 4. Data Management: Oversee data collection, management, and quality control. 5. Communication: Facilitate communication among study sites, sponsors, and other stakeholders. 6. Problem-Solving: Identify and resolve issues that arise during the study. 7. Documentation: Maintain accurate and complete study documentation. Requirements: 1. Education: Bachelor's degree in a life science, nursing, or related field. 2. Experience: 5 to 6 experience in clinical research coordination. 3. Skills: Strong organizational, communication, and problem-solving skills. 4. Knowledge: Familiarity with GCP, regulatory requirements, and clinical trial operations. Desirable Skills: 1. Certification: Certification in clinical research coordination (e.g., CCRA or CCRC). 2. Experience with Clinical Trial Management Systems (CTMS): Familiarity with CTMS and electronic data capture (EDC) systems. Job Types: Full-time, Permanent Pay: ₹45,000.00 - ₹50,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Fixed shift Work Location: In person Application Deadline: 20/07/2025
Job Summary: We are seeking a proactive male Clinical Research Coordinator with 1–2 years of experience in clinical trial coordination. The ideal candidate will assist in the smooth conduct of clinical trials at the site level, ensuring adherence to protocol, GCP, and applicable regulatory standards. Key Responsibilities: Assist in planning and execution of clinical trials under the supervision of the Principal Investigator. Coordinate participant screening, recruitment, informed consent, and enrollment. Conduct subject visits and ensure protocol procedures, data collection, and documentation are performed accurately and on time. Maintain all study-related records, including source documents, CRFs, logs, and investigator files. Manage study supplies and investigational product (IP) as per protocol and SOPs. Liaise with sponsors, CRAs, and vendors during monitoring visits or audits. Ensure safety reporting (AE/SAE) is timely and accurate. Coordinate logistics of subject follow-ups and sample shipment, including occasional off-site or late-hour coordination when necessary. Support regulatory documentation, submissions, and communications with the Ethics Committee. Maintain confidentiality and ethical conduct throughout the study duration. Required Qualifications: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or equivalent. 1–2 years of experience working as a CRC or Clinical Trial Assistant. Basic understanding of GCP, clinical trial conduct, and ethics guidelines. Good verbal and written communication skills. Ability to multitask, maintain accuracy, and work independently. Willingness to travel locally and work flexible hours when required. Desirable Skills: Experience in managing Phase II/III clinical trials. Familiarity with electronic data capture (EDC) systems. Previous interaction with sponsors, CROs, and Ethics Committees. Job Type: Full-time Pay: From ₹20,000.00 per month Benefits: Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Ability to commute/relocate: Peenya, Bengaluru, Karnataka: Reliably commute or planning to relocate before starting work (Preferred) Education: Master's (Preferred) Experience: Clinical research: 1 year (Required) Language: English (Required) Work Location: In person Application Deadline: 31/07/2025 Expected Start Date: 23/07/2025
As a Medical Writer with our dynamic team, you will utilize your expertise in writing, editing, and reviewing scientific and medical content. Your primary responsibility will involve transforming intricate medical data and research findings into clear, accurate, and engaging documents suitable for various audiences, including healthcare professionals, regulatory bodies, and the general public. You will be expected to develop, write, and edit a diverse range of documents such as clinical study reports, regulatory submission documents, peer-reviewed publications, and educational materials. Your role will also involve generating high-quality manuscripts, abstracts, posters, and presentations for scientific conferences, journals, and other platforms. Collaboration is key in this role as you will work closely with researchers, clinicians, regulatory affairs professionals, and other stakeholders to ensure that all content aligns with regulatory standards, maintains scientific accuracy, and supports corporate objectives. Additionally, you will be responsible for preparing and revising documents for regulatory submissions, ensuring compliance with guidelines from regulatory bodies such as FDA, EMA, and ICH. Your tasks will also include conducting literature searches, reviewing existing medical research, and ensuring the accuracy and relevance of information to support content development. Quality assurance is crucial as you will be editing and proofreading content for clarity, consistency, accuracy, grammar, and adherence to style guides. Project management skills are essential as you will be managing timelines for multiple projects to ensure timely and efficient completion of tasks. Compliance with medical, ethical, and regulatory standards is a core requirement for this role. To qualify for this position, you should hold a degree in BAMS, BDS, MBBS, or Pharm D, along with a minimum of 2 years of experience in medical writing, medical coding, or a related field. Experience with regulatory documents is highly preferred. A strong understanding of clinical research, medical terminology, and regulatory guidelines is essential. Proficiency in Microsoft Office Suite, reference management software, and medical writing software is required. Excellent written and verbal communication skills are essential, with the ability to convey complex information clearly and concisely. Strong attention to detail, collaboration skills, and the capability to work independently and as part of a team in a fast-paced environment are also necessary. Exceptional command of the English language is required, and knowledge of additional languages is a plus. Desirable skills for this role include experience with writing for regulatory agencies, familiarity with scientific publishing and journal submission processes, knowledge of Good Clinical Practice (GCP), and experience with statistical analysis and interpretation of clinical data. This is a full-time, permanent position with benefits including provided food, health insurance, and Provident Fund. The work schedule is a day shift with a fixed location in person. The application deadline is 31/07/2025.,
As a Junior Accountant, you will play a crucial role in supporting the Finance Department by managing day-to-day accounting tasks. Your responsibilities will include recording financial transactions accurately, assisting in bank reconciliations and expense tracking, and contributing to the monthly and year-end closing processes. You will be pivotal in preparing financial reports, ensuring compliance with accounting standards and company policies, and liaising with internal departments and external vendors for invoice processing. To excel in this role, you should hold a Bachelor's degree in Commerce, Accounting, or Finance, coupled with at least 2 years of relevant experience in accounting or finance. Proficiency in accounting principles, financial regulations, and working with accounting software such as Tally is essential. Strong organizational skills, attention to detail, and familiarity with MS Excel and other MS Office tools are qualities that will aid in your success. Your ability to communicate effectively, collaborate within a team, and meet deadlines will be critical. Preferred skills include knowledge of GST, TDS, and ERP systems. The role requires full-time availability and is suited for male candidates. In return, we offer benefits such as provided meals, health insurance, and Provident Fund. The work schedule is during day shifts with fixed timings. The job location is in Bangalore, Karnataka, requiring in-person attendance. If you are dedicated to advancing your career in accounting and finance, we welcome your application before the deadline of 21/07/2025.,
Job Summary: We are seeking a motivated and tech-savvy IT Support Intern to join our IT team. The intern will assist in providing technical support, troubleshooting hardware and software issues, and helping maintain the organization’s IT infrastructure. This is a great opportunity to gain hands-on experience in a real-world IT environment. Key Responsibilities: Assist in providing first-level technical support to end-users via phone, email, or in person. Troubleshoot hardware, software, and network-related issues. Help with the setup, configuration, and maintenance of computer systems and peripherals. Install and update software applications and operating systems. Support IT team in maintaining inventory of hardware and software assets. Assist in managing user accounts, passwords, and access rights. Document technical issues and resolutions in the IT ticketing system. Participate in IT projects as required (e.g., system upgrades, migration, etc.). Maintain confidentiality and security of data and systems. Requirements: Currently pursuing a degree/diploma in Computer Science, Computer Applications, Information Technology, or related field. Basic knowledge of operating systems (Windows/Linux), networking, and common software applications. Strong analytical and problem-solving skills. Good communication skills and a willingness to learn. Ability to work independently and in a team environment. What You Will Gain: Hands-on experience in IT support and system administration. Exposure to enterprise IT tools and practices. Opportunity to work with experienced IT professionals. Certificate of Internship and Letter of Recommendation (based on performance). Job Types: Contractual / Temporary, Internship Contract length: 3 months Pay: From ₹4,500.00 per month Benefits: Food provided Paid sick time Work Location: In person
Job Summary The Research Associate Trainee – Biochemistry will support laboratory research activities in biochemical and life sciences projects. The role involves conducting experiments, maintaining accurate data records, and assisting senior researchers in ongoing studies. This is an entry-level trainee position designed to provide hands-on training and exposure to various biochemical techniques, instrumentation, and laboratory practices. Job Description / Responsibilities Preparation of samples for biochemical analysis. Recording raw data accurately in worksheets, logbooks, and other analytical documentation. Reporting deviations, abnormalities, or non-conformities promptly to the Technical Manager. Operating, maintaining, and performing calibration of laboratory equipment. Monitoring and documenting environmental conditions such as humidity and temperature within the department. Managing samples within the department, including receipt, storage, usage, and documentation. Preparing and labeling samples, standards, and related documents as per SOPs. Recording process conditions used for sample preparation in registers or electronic systems. Maintaining equipment used for sample preparation, ensuring proper functionality and cleanliness. Performing internal calibrations and documenting results as per quality requirements. Archival of samples and maintenance of related records. Ensuring compliance with Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), and management systems. Maintaining high standards of laboratory housekeeping and safety Qualifications & Skills Diploma in Medical Laboratory (DMLT)/ Bachelor of Medical Laboratory Technology (BMLT). Strong understanding of biochemical techniques and laboratory practices. Familiarity with laboratory equipment operation, calibration, and maintenance. Good documentation skills with attention to accuracy and detail. Ability to work independently as well as in a team. Commitment to quality, safety, and compliance standards. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Food provided Health insurance Paid sick time Provident Fund Work Location: In person
Job Summary The Laboratory Technician will be responsible for performing histopathology procedures, hematology, and biochemical analyses of biological samples as per study design and GLP requirements. The role involves accurate data recording, equipment maintenance, and ensuring compliance with SOPs, GLP, and regulatory standards. Key Responsibilities Perform dissection, processing, embedding, sectioning, and staining of tissue specimens as per study protocols. Ensure accuracy and quality at every stage of histopathology procedures. Prepare and forward histology slides to pathologists for review and reporting. Conduct hematology analyses for both preclinical and clinical samples. Perform biochemical analysis of biological samples (urine, blood, saliva, etc.). Operate, calibrate, and maintain laboratory equipment as per defined schedules. Accurately record observations and results in raw data sheets; ensure systematic documentation. Archive samples, reports, and raw data, maintaining compliance with documentation standards. Monitor temperature, humidity, and other environmental conditions in testing areas as per requirements. Prepare and label documents, samples, and standards appropriately. Report equipment malfunctions or abnormalities to the Technical Manager. Follow Good Laboratory Practices (GLP), Standard Operating Procedures (SOPs), and internal management systems. Maintain laboratory cleanliness, safety, and regulatory compliance. Complete assigned tasks within specified deadlines. Qualifications & Skills Diploma in Medical Laboratory (DMLT)/ Bachelor of Medical Laboratory Technology (BMLT). Prior experience in histopathology, hematology, or clinical biochemistry preferred. Knowledge of GLP guidelines, laboratory safety, and regulatory compliance. Hands-on experience with tissue processing, sectioning, staining, and clinical sample analysis. Proficiency in handling and calibrating laboratory instruments. Strong attention to detail and documentation skills. Ability to work independently as well as in a team environment. Experience 3–4 years of experience in a research/diagnostic laboratory setting preferred. Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Food provided Health insurance Paid sick time Provident Fund Work Location: In person
Job Summary The Research Associate Trainee – Biochemistry will support laboratory research activities in biochemical and life sciences projects. The role involves conducting experiments, maintaining accurate data records, and assisting senior researchers in ongoing studies. This is an entry-level trainee position designed to provide hands-on training and exposure to various biochemical techniques, instrumentation, and laboratory practices. Job Description / Responsibilities Preparation of samples for biochemical analysis. Recording raw data accurately in worksheets, logbooks, and other analytical documentation. Reporting deviations, abnormalities, or non-conformities promptly to the Technical Manager. Operating, maintaining, and performing calibration of laboratory equipment. Monitoring and documenting environmental conditions such as humidity and temperature within the department. Managing samples within the department, including receipt, storage, usage, and documentation. Preparing and labeling samples, standards, and related documents as per SOPs. Recording process conditions used for sample preparation in registers or electronic systems. Maintaining equipment used for sample preparation, ensuring proper functionality and cleanliness. Performing internal calibrations and documenting results as per quality requirements. Archival of samples and maintenance of related records. Ensuring compliance with Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), and management systems. Maintaining high standards of laboratory housekeeping and safety Qualifications & Skills Diploma in Medical Laboratory (DMLT)/ Bachelor of Medical Laboratory Technology (BMLT). Strong understanding of biochemical techniques and laboratory practices. Familiarity with laboratory equipment operation, calibration, and maintenance. Good documentation skills with attention to accuracy and detail. Ability to work independently as well as in a team. Commitment to quality, safety, and compliance standards. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Food provided Health insurance Paid sick time Provident Fund Work Location: In person
Job Summary The Laboratory Technician will be responsible for performing histopathology procedures, hematology, and biochemical analyses of biological samples as per study design and GLP requirements. The role involves accurate data recording, equipment maintenance, and ensuring compliance with SOPs, GLP, and regulatory standards. Key Responsibilities Perform dissection, processing, embedding, sectioning, and staining of tissue specimens as per study protocols. Ensure accuracy and quality at every stage of histopathology procedures. Prepare and forward histology slides to pathologists for review and reporting. Conduct hematology analyses for both preclinical and clinical samples. Perform biochemical analysis of biological samples (urine, blood, saliva, etc.). Operate, calibrate, and maintain laboratory equipment as per defined schedules. Accurately record observations and results in raw data sheets; ensure systematic documentation. Archive samples, reports, and raw data, maintaining compliance with documentation standards. Monitor temperature, humidity, and other environmental conditions in testing areas as per requirements. Prepare and label documents, samples, and standards appropriately. Report equipment malfunctions or abnormalities to the Technical Manager. Follow Good Laboratory Practices (GLP), Standard Operating Procedures (SOPs), and internal management systems. Maintain laboratory cleanliness, safety, and regulatory compliance. Complete assigned tasks within specified deadlines. Qualifications & Skills Diploma in Medical Laboratory (DMLT)/ Bachelor of Medical Laboratory Technology (BMLT). Prior experience in histopathology, hematology, or clinical biochemistry preferred. Knowledge of GLP guidelines, laboratory safety, and regulatory compliance. Hands-on experience with tissue processing, sectioning, staining, and clinical sample analysis. Proficiency in handling and calibrating laboratory instruments. Strong attention to detail and documentation skills. Ability to work independently as well as in a team environment. Experience 3–4 years of experience in a research/diagnostic laboratory setting preferred. Job Type: Full-time Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Food provided Health insurance Paid sick time Provident Fund Work Location: In person