We are looking for motivated and goal-oriented individuals to join our Admissions Team. The ideal candidate should be enthusiastic about education and career development, and capable of handling the entire sales cycle—from initial contact to final enrollment. Freshers with excellent communication and a passion for sales are welcome to apply. Experienced candidates should have a proven track record of closing deals and meeting targets. Responsibilities Guide prospective students and parents about course offerings, career outcomes, certifications, and institute benefits. Understand candidates’ backgrounds and suggest appropriate courses or training programs. Follow up on inquiries and leads to convert interest into confirmed admissions. Achieve monthly and quarterly admission targets. Prepare daily/weekly reports on performance, lead status, and conversions. Qualifications Any graduate Experience in full sales cycle including deal closing Demonstrated sales success Strong negotiation skills Strong communication and presentation skills Show more Show less

Responsibilities: Collect and process adverse event reports from clinical trials and post-marketing sources Perform case triage, data entry, and quality checks in safety databases Assist in preparation of regulatory reports (e.g., CIOMS, MedWatch) Conduct literature screening for safety data Ensure compliance with global pharmacovigilance regulations and SOPs Job Types: Full-time, Fresher Pay: ₹286,000.00 - ₹970,000.00 per year Benefits: Health insurance Schedule: Day shift Work Location: In person

Tips: Provide a summary of the role, what success in the position looks like, and how this role fits into the organization overall. Responsibilities Guide prospective students and parents about course offerings, career outcomes, certifications, and institute benefits. Understand candidates’ backgrounds and suggest appropriate courses or training programs. Follow up on inquiries and leads to convert interest into confirmed admissions. Achieve monthly and quarterly admission targets. Prepare daily/weekly reports on performance, lead status, and conversions. Qualifications Any Graduate Show more Show less

Key Responsibilities Guide prospective students and parents about course offerings, career outcomes, certifications, and institute benefits. Understand candidates’ backgrounds and suggest appropriate courses or training programs. Follow up on inquiries and leads to convert interest into confirmed admissions. Achieve monthly and quarterly admission targets. Prepare daily/weekly reports on performance, lead status, and conversions. About Company: Fusion Technology Solutions is one of the best skill development training institutes, offering a wide range of courses under one roof. We provide training across various industry sectors, including healthcare/medical with clinical research, medical coding, and pharmacovigilance courses; aviation, offering cabin crew and ground staff courses; IT, featuring PHP, JAVA, Stack Development courses, and more; research, including market research and data science courses; and marketing, with a comprehensive digital marketing course. Show more Show less

Duties: Accurately document patient visits and clinical data Update EHRs with medical history, lab results, and procedures Assist with administrative tasks related to patient records Ensure compliance with confidentiality and privacy regulations Skills Required: Excellent written communication Strong understanding of medical terminology Fast and accurate typing Attention to detail and confidentiality Job Type: Full-time Pay: ₹16,000.00 - ₹23,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Responsibilities: Identify and research potential clients and markets Generate leads and convert them into business opportunities Build and maintain strong client relationships Prepare and present business proposals and sales pitches Collaborate with marketing and product teams to align strategies Meet and exceed sales targets and KPIs

Tips: Provide a summary of the role, what success in the position looks like, and how this role fits into the organization overall. Responsibilities 1 . Conduct in-person and virtual training sessions, workshops, and seminars on clinical research processes, GCP, ethical guidelines, safety reporting, and trial protocols. 2 Create and maintain curriculum, training materials, and e-learning content for clinical research personnel. 3 Conducting sessions on clinical research, clinical data management, pharmacovigilance, medical Coding. Qualifications B.Pharm, M. pharm, pharm D, Any Life Science Graduate. Show more Show less

Responsibilities: Monitor and manage clinical trial sites Ensure compliance with protocols and regulations (e.g., GCP, FDA) Verify accuracy of patient data and clinical records Train site staff on trial procedures Prepare reports and assist in audits or inspections Job Type: Full-time Pay: ₹15,000.00 - ₹38,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Responsibilities: Conduct lab tests and experiments on microbes Analyze samples from humans, animals, or the environment Identify microorganisms and monitor their effects Develop antibiotics, vaccines, or biotechnological products Maintain lab equipment and ensure safety standards Job Type: Full-time Pay: ₹18,000.00 - ₹38,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Responsibilities: Maintain and organize Trial Master File (TMF) and essential documents. Track study progress, including patient enrollment and site communications. Assist with the preparation and submission of regulatory documents. Schedule meetings, take minutes, and support trial team coordination. Ensure compliance with Good Clinical Practice (GCP) and applicable regulations. Job Type: Full-time Pay: ₹20,000.00 - ₹45,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Responsibilities: Write and edit clinical study reports, protocols, regulatory submissions, and manuscripts. Translate complex scientific data into understandable content for various audiences. Ensure documents comply with regulatory guidelines (e.g., ICH, FDA, EMA). Collaborate with cross-functional teams, including clinical, regulatory, and marketing. Conduct literature reviews and stay updated on therapeutic areas and medical writing trends. Job Type: Full-time Pay: ₹20,000.00 - ₹45,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Responsibilities: Maintain and organize Trial Master File (TMF) and essential documents. Track study progress, including patient enrollment and site communications. Assist with the preparation and submission of regulatory documents. Schedule meetings, take minutes, and support trial team coordination. Ensure compliance with Good Clinical Practice (GCP) and applicable regulations. Job Type: Full-time Pay: ₹20,000.00 - ₹45,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Responsibilities: Document patient history, symptoms, and physical exam findings during clinical visits Accurately input provider’s assessment and treatment plans into the electronic health record (EHR) Review and update patient charts and follow-up information Assist in maintaining compliance with legal and ethical documentation standards Work closely with physicians and healthcare staff in a fast-paced environment Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Responsibilities: Document patient history, symptoms, and physical exam findings during clinical visits Accurately input provider’s assessment and treatment plans into the electronic health record (EHR) Review and update patient charts and follow-up information Assist in maintaining compliance with legal and ethical documentation standards Work closely with physicians and healthcare staff in a fast-paced environment Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Health insurance Schedule: Day shift Work Location: In person

Key Responsibilities Conduct in-person and virtual training sessions, workshops, and seminars on clinical research processes, GCP, ethical guidelines, safety reporting, and trial protocols. Create and maintain curriculum, training materials, and e-learning content for clinical research personnel. Conduct sessions on clinical research, clinical data management, pharmacovigilance, and medical coding. About Company: Fusion Technology Solutions is one of the best skill development training institutes, offering a wide range of courses under one roof. We provide training across various industry sectors, including healthcare/medical with clinical research, medical coding, and pharmacovigilance courses; aviation, offering cabin crew and ground staff courses; IT, featuring PHP, JAVA, Stack Development courses, and more; research, including market research and data science courses; and marketing, with a comprehensive digital marketing course.

The responsibilities for this role include managing and overseeing the collection, processing, and storage of clinical trial data to ensure data integrity and accuracy. You will be responsible for maintaining databases, performing data entry tasks, and collaborating with clinical research teams to ensure data compliance with regulatory standards. The ideal candidate should possess strong organizational and data management skills, have attention to detail and accuracy, be proficient in data management software, and demonstrate excellent communication and teamwork abilities. This is a full-time position suitable for freshers. The benefits include health insurance. The work schedule is during the day shift, and the work location is in person.,

key duties Monitoring and Reporting : Tracking and documenting adverse drug reactions (ADRs) and ensuring they are reported to regulatory authorities. Data Collection & Analysis : Reviewing clinical trial and post-marketing data to identify trends in drug safety. Compliance : Ensuring adherence to regulatory guidelines and company policies regarding drug safety and pharmacovigilance. Collaboration : Working with medical, regulatory, and clinical teams to ensure comprehensive drug safety reporting. Safety Reviews : Assessing and providing recommendations on risk management strategies for drugs. Job Type: Full-time Pay: ₹350,000.00 - ₹675,000.00 per year Benefits: Health insurance Work Location: In person

Key Responsibilities: Conduct GCP audits (e.g., site, vendor, document, system audits). Ensure clinical trial compliance with FDA, EMA, ICH, and other regulatory bodies. Identify quality issues and collaborate on corrective/preventive actions (CAPAs). Support inspection readiness and regulatory agency audits. Maintain quality documentation and QA metrics. Job Type: Full-time Pay: ₹330,000.00 - ₹650,000.00 per year Benefits: Health insurance Work Location: In person

You will be responsible for collecting and entering clinical trial data from various sources, ensuring that it complies with study protocols and regulatory standards. Additionally, you will review the data for discrepancies, missing values, and inconsistencies, perform data cleaning, and uphold data quality standards. You will also be tasked with identifying, escalating, and resolving data queries in collaboration with clinical teams and study sites. In this role, you will maintain and manage essential study documents such as case report forms (CRFs), data management plans, and databases. Effective collaboration with Clinical Research Associates (CRAs), Clinical Data Managers, and other stakeholders is essential to ensure the timely and accurate collection of data. Furthermore, you will provide support for the maintenance and configuration of data management systems and software to guarantee the smooth flow of data. This position is full-time and requires work to be conducted in person. The benefits offered for this position include health insurance.,

Key Responsibilities: Perform data entry, validation, and cleaning in clinical databases (e.g., Medidata, Oracle Clinical). Identify and resolve data discrepancies by raising and managing queries with study sites. Ensure timely and accurate database updates throughout the study lifecycle. Collaborate with Clinical Data Managers, CRAs, and biostatisticians. Assist in database lock and audit readiness. Job Type: Full-time Pay: ₹18,500.00 - ₹45,000.00 per month Benefits: Health insurance Work Location: In person