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.,