We Are CRO Based Company Helping in Clinical Trials

Company OverviewPharmabharat is a Clinical Research Organization (CRO) dedicated to advancing clinical trials in the Hospitals and Health Care industry. With its headquarters in Maharashtra, our team of 11-50 employees is committed to supporting cutting-edge healthcare solutions. For more information, visit our website at <a href="https://pharmabharat.com/" rel="noopener noreferrer" target="_blank">Pharmabharat.com</a>. Job OverviewWe are looking for a Regulatory Affairs Trainee to join our team. This is a full-time position suitable for freshers with 0 to 1 year of experience. The job will be based in major cities, including Pune, Mumbai, Hyderabad, and Bangalore Urban. The trainee will be responsible for supporting regulatory compliance and submission activities in line with industry standards. Qualifications and Skills<ul><li>Regulatory Compliance (Mandatory skill): Profound understanding of regulatory frameworks within the pharmaceutical industry essential.</li><li>FDA Regulations (Mandatory skill): Familiarity with FDA guidelines and processes for new drug approvals is critical.</li><li>Pharmaceutical Regulations (Mandatory skill): Must adhere to comprehensive pharmaceutical laws and regulations at all times.</li><li>Documentation Management: Aptitude for maintaining and managing regulatory documentation accurately and methodically.</li><li>Quality Assurance: Skills to ensure that all regulatory activities comply with quality assurance standards and practices.</li><li>Medical Device Regulations: Understanding of regulations concerning medical devices and the ability to apply them to internal processes.</li><li>Regulatory Submissions: Ability to support the preparation and submission of regulatory filings to local health authorities.</li><li>Regulatory Reporting: Capable of assisting with regulatory reporting tasks, ensuring timely and accurate submissions.</li></ul> Roles and Responsibilities<ul><li>Assist in preparing and compiling necessary documents for regulatory submissions.</li><li>Ensure compliance with regulatory policies and guidelines for all operations.</li><li>Maintain up-to-date knowledge of global regulatory requirements and industry standards.</li><li>Coordinate with internal teams to gather necessary information for submission processes.</li><li>Participate in regulatory audits and implement corrective action plans as needed.</li><li>Contribute to the development and maintenance of regulatory databases and systems.</li><li>Support the development of strategies to streamline regulatory processes.</li><li>Communicate effectively with cross-functional teams to ensure alignment on regulatory affairs objectives.</li></ul>

Company OverviewPharmabharat is a CRO based company specializing in aiding clinical trials. With a dedicated team of 11-50 employees, we are headquartered in Maharashtra and belong to the Hospitals and Health Care industry. Our mission is to advance health research by providing expert clinical trial management. For more information, visit our website at <a href="https://pharmabharat.com/" rel="noopener noreferrer" target="_blank">pharmabharat.com</a>. Job OverviewWe are seeking a Clinical Data Management Lead to join our team at Pharmabharat. This full-time, mid-level position is based in Pune Division, Kolkata, or Mumbai. The successful candidate will have 4 to 6 years of experience, with expertise in clinical trials and data management. The role involves leading data management projects and ensuring compliance with industry standards. Qualifications and Skills<ul><li>Proficiency in clinical trials, ensuring data integrity and accuracy throughout the trial phases (Mandatory skill).</li><li>Strong command over data management practices to effectively collect, process, and manage trial data (Mandatory skill).</li><li>Experienced in project management to coordinate cross-functional team efforts and meet project milestones on time (Mandatory skill).</li><li>In-depth knowledge of CDISC standards to ensure structured and standardized data reporting.</li><li>Ability to implement rigorous quality control measures to maintain high data quality and compliance.</li><li>Expertise in database programming, facilitating the design and maintenance of effective data management systems.</li><li>Proven leadership abilities to mentor and guide a team of data management professionals.</li><li>Understanding of regulatory compliance to ensure all data processes adhere to industry standards and laws.</li></ul> Roles and Responsibilities<ul><li>Lead and manage clinical data management projects from initiation to completion, ensuring all project objectives are met.</li><li>Collaborate with cross-functional teams to design and implement data management plans that comply with required standards.</li><li>Ensure the integrity, accuracy, and confidentiality of clinical trial data throughout all project phases.</li><li>Oversee database design, development, testing, and implementation for clinical studies.</li><li>Perform regular quality checks and audits to ensure adherence to data management processes and regulatory standards.</li><li>Mentor and guide junior data management staff, fostering a collaborative and learning-oriented environment.</li><li>Work closely with project managers and stakeholders to ensure timely delivery of data-related project milestones.</li><li>Communicate effectively with internal and external stakeholders to address any data management issues or requirements.</li></ul>

Company OverviewPharmabharat is a CRO-based company dedicated to assisting in clinical trials, with its headquarters located in Maharashtra. Operating within the hospitals and health care industry, Pharmabharat is a small enterprise employing between 11 to 50 professionals. For more information, please visit our website at <a href="https://pharmabharat.com/" rel="noopener noreferrer" target="_blank">pharmabharat.com</a>. Job OverviewWe are seeking a Clinical Research Associate for our operations based in Pune Division, Hyderabad, and Bangalore Urban. This is a full-time position ideal for freshers, requiring between 0 to 1 year of work experience. The selected candidate will be involved in a range of activities related to clinical trial management, regulatory compliance, and protocol development. Qualifications and Skills<ul><li>Clinical trial management (Mandatory skill) - Ability to plan, execute, and manage clinical trials ensuring adherence to outlined protocols and schedules.</li><li>Regulatory compliance (Mandatory skill) - Ensuring all clinical trial operations and practices comply with local, national, and hospital regulations.</li><li>Protocol development (Mandatory skill) - Expertise in developing protocols for drug trials, ensuring they align with scientific and regulatory standards.</li><li>Data collection and analysis - Skillful in collecting, analyzing, and interpreting data related to clinical trial results and findings.</li><li>Good Clinical Practice (GCP) - Proficient in maintaining the standards for conducting, recording, and reporting clinical trials involving human subjects.</li><li>Medical terminology - Understanding of medical language crucial for accurately interpreting and discussing clinical trial data.</li><li>Patient recruitment - Ability to effectively identify, recruit, and engage potential participants for clinical trials.</li><li>Report writing - Experienced in writing detailed reports to present findings, methodologies, and results of clinical research.</li></ul> Roles and Responsibilities<ul><li>Monitor clinical trials to ensure compliance with regulatory requirements and study protocols.</li><li>Facilitate communication between research sites and the project management team to ensure seamless study coordination.</li><li>Coordinate with medical and statistical staff to prepare study material and presentations.</li><li>Oversee patient recruitment processes, ensuring the recruitment targets are met within deadlines.</li><li>Collect and review clinical data to ensure accuracy and consistency as per the trial's design.</li><li>Participate in study site initial, interim, and close-out visit activities, focusing on protocol adherence and patient safety.</li><li>Prepare and submit detailed reports on trial progress, ensuring transparency and communication among stakeholders.</li><li>Engage in regular training updates to maintain clinical trial management and good clinical practice standards.</li></ul>

Sun Pharma is the&nbsp;fourth largest specialty generic pharmaceutical company in the world&nbsp;and&nbsp;India’s largest pharmaceutical company by market capitalization. We provide high-quality, affordable medicines that are trusted by healthcare professionals and patients in over&nbsp;150 countries. To support our growth, we are looking for young and energetic professionals for&nbsp;multiple locations. Apply Here: <a href="https://pharmabharat.com/sun-pharmaceutical-hiring-for-b-pharm-m-pharm-iti-diploma/" rel="noopener noreferrer" target="_blank">https://pharmabharat.com/sun-pharmaceutical-hiring-for-b-pharm-m-pharm-iti-diploma/</a> <h3>Job Details</h3><h4>Department:</h4>Manufacturing (OSD/Tablet)<h4>Role:</h4>Technician – Executive<h3>Qualifications</h3><ul><li>B.Pharm</li><li>M.Pharm</li><li>ITI</li><li>Diploma</li></ul><h3>Experience</h3><ul><li>2–5+ years&nbsp;of relevant experience in the pharmaceutical manufacturing industry.</li></ul><h3>Key Responsibilities</h3><ul><li>Perform tasks related to the&nbsp;manufacturing of OSD (Oral Solid Dosage)&nbsp;forms such as tablets.</li><li>Ensure compliance with&nbsp;Good Manufacturing Practices (GMP)&nbsp;and company protocols.</li><li>Operate and maintain equipment to ensure efficiency and safety.</li><li>Collaborate with the team for process improvements and troubleshooting.</li></ul>

Company OverviewPharmabharat is a CRO based company that supports clinical trials and is part of the Hospitals and Health Care industry. With a team of 11-50 employees, we are dedicated to advancing healthcare by providing comprehensive clinical trial services. Our headquarters are located in Maharashtra, and you can learn more about us at <a href="https://pharmabharat.com/" rel="noopener noreferrer" target="_blank">pharmabharat.com</a>. Job OverviewWe are seeking a Pharmacovigilance Trainee to join our team. This is a full-time, entry-level position ideal for freshers with 0 to 1 year of work experience. The role will be based in Pune, Nashik, Mumbai, or Bangalore Urban. As a Pharmacovigilance Trainee, you will play a crucial role in ensuring the safety and efficacy of pharmaceuticals by monitoring drug safety and reporting adverse effects. Qualifications and Skills<ul><li>Proficiency in statistical analysis for evaluating clinical trial data (Mandatory skill)</li><li>Experience with predictive modeling techniques to forecast pharmaceutical outcomes (Mandatory skill)</li><li>Knowledge of big data technologies and their application in pharmacovigilance (Mandatory skill)</li><li>Understanding of machine learning algorithms and their use in healthcare data</li><li>Solid foundation in Python programming for data analysis</li><li>Ability to visualize data effectively to support decision-making processes</li><li>Experience with SQL for database management and querying</li><li>Skills in data mining to extract valuable insights from large datasets</li></ul> Roles and Responsibilities<ul><li>Monitor, detect, assess, and report adverse effects of pharmaceutical products</li><li>Assist in the analysis and interpretation of clinical trial data</li><li>Utilize statistical tools to evaluate drug safety and efficacy</li><li>Develop predictive models to anticipate potential adverse reactions</li><li>Manage and analyze large datasets to identify trends and patterns</li><li>Create data visualizations to effectively communicate findings</li><li>Collaborate with cross-functional teams to ensure regulatory compliance</li><li>Maintain accurate and detailed records of all pharmacovigilance activities</li></ul> Click Here &lt;pharmabharat.com&gt; To Apply