Help us bring cutting-edge medical treatments to life! Become a key player in clinical research and accelerate advancements in healthcare.OpportunitiesWe offer two paths into the exciting world of clinical research:Internship: Get a hands-on introduction to clinical trials through a time-bound internship program. Ideal for students or recent graduates eager to experience the field.Fresher-Level Position: Launch your career as a Clinical Research Coordinator! This position offers ongoing employment for those committed to this exciting field.Regardless of path, you'll get to:Manage the flow of clinical trials: Oversee study logistics, participant documentation, and ensure the study progresses smoothly.Be a meticulous record-keeper: Collect and safeguard essential research data with the highest industry standards.Champion safety and ethics: Protect patient rights and ensure all research practices are ethical and compliant.Work within a team of like-minded professionals: Collaborate with investigators, healthcare providers, and fellow research enthusiasts.QualificationsInternship: Enrolled in or a recent graduate of a degree program in life sciences, health sciences, nursing, or a related field.Fresher-Level Position: Recent graduate with a degree in life sciences, health sciences, nursing, or a related field.For both: Passion for research, detail-orientation, strong organizational skills, clear communication, and willingness to learn.What We OfferHands-on experience: Jumpstart your career or get real-world training.Training and mentorship: Get guidance from experienced researchers in the field.Professional development: Access resources or company-sponsored coursework to enhance your potential.Competitive compensation: Interns receive a stipend; fresher-level position offers salary and benefits.A role at the forefront of medical innovation: Shape the future of healthcare.

We are seeking a highly motivated and detail-oriented recent graduate to join our Pharmacovigilance team as an Entry-Level Pharmacovigilance Associate. This is a fantastic opportunity to begin your career in the pharmaceutical industry and contribute to the safety monitoring of our products. You will gain hands-on experience in various aspects of pharmacovigilance, including adverse event reporting, data entry, and case processing. This role is ideal for individuals with a strong interest in drug safety and a desire to learn and grow in a dynamic environment.Responsibilities:Adverse Event Case Processing: Receive, triage, and accurately enter adverse event reports into the pharmacovigilance database.Ensure timely and accurate data entry according to company Standard Operating Procedures (SOPs) and regulatory guidelines.Assist in the follow-up of adverse event reports to obtain complete information.Perform quality checks on case data to ensure accuracy and consistency.Data Management and Reporting: Assist in the preparation of safety reports and data summaries.Maintain accurate and organized pharmacovigilance records.Assist in the tracking and monitoring of adverse event trends.Regulatory Compliance: Gain a basic understanding of global pharmacovigilance regulations and guidelines.Adhere to company SOPs and regulatory requirements.Assist in the preparation of regulatory submissions.General Support: Assist in the maintenance of pharmacovigilance databases and systems.Participate in team meetings and training sessions.Support senior pharmacovigilance staff as needed.Any other duties as assigned.Qualifications:Bachelor's degree in Pharmacy, Pharmacology, Life Sciences, Nursing, or a related healthcare field.Strong interest in drug safety and pharmacovigilance.Excellent attention to detail and accuracy.Strong organizational and time-management skills.Ability to work independently and as part of a team. Good communication and interpersonal skills.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Must be a recent graduate.

We are seeking a highly motivated and detail-oriented recent graduate to join our Drug Safety team as an Entry-Level Drug Safety Associate. This is an excellent opportunity to launch your career in the pharmaceutical industry and contribute to the safety surveillance of our products. You will gain practical experience in various aspects of drug safety, including adverse event processing, data entry, and safety reporting. This role is perfect for individuals with a strong interest in drug safety and a desire to learn and grow in a fast-paced environment.Responsibilities:Adverse Event Case Processing: Receive, triage, and accurately enter adverse event reports into the drug safety database.Ensure timely and accurate data entry in compliance with company Standard Operating Procedures (SOPs) and regulatory guidelines.Assist in the follow-up of adverse event reports to obtain complete and accurate information.Perform quality control checks on case data to ensure accuracy and consistency.Data Management and Safety Reporting: Assist in the preparation of safety reports and data summaries.Maintain accurate and organized drug safety records.Assist in the tracking and monitoring of adverse event trends.Learn to identify and escalate potential safety signals.Regulatory Compliance: Develop a basic understanding of global drug safety regulations and guidelines (e.g., ICH guidelines).Adhere to company SOPs and regulatory requirements.Assist in the preparation of regulatory submissions.General Support: Assist in the maintenance of drug safety databases and systems.Participate in team meetings and training sessions.Support senior drug safety staff as needed.Perform other duties as assigned.Qualifications:Bachelor's degree in Pharmacy, Pharmacology, Life Sciences, Nursing, or a related healthcare field.Strong interest in drug safety and pharmacovigilance.Excellent attention to detail and accuracy.Strong organizational and time-management skills.Ability to work independently and collaboratively within a team. Good communication and interpersonal skills. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).Must be a recent graduate.Preferred Qualifications (but not required):Basic understanding of medical terminology.Familiarity with drug safety databases or systems.Coursework related to pharmacology or drug safety.

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator (Fresher) to join our dynamic clinical research team. In this role, you will play a crucial part in ensuring the successful execution of our clinical trials from start to finish. You will collaborate with a multidisciplinary team of researchers, investigators, and study personnel to coordinate all aspects of clinical trial operations.Key Responsibilities:Study Coordination: Coordinate the day-to-day activities of assigned clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements.Site Management: Assist in site selection, initiation, monitoring, and close-out activities.Documentation: Maintain accurate and complete study records, including case report forms, source documents, and regulatory binders.Communication: Facilitate effective communication between study sites, sponsors, investigators, and internal team members.Data Management: Ensure timely and accurate data collection, entry, and query resolution.Regulatory Compliance: Ensure compliance with all applicable regulations, guidelines, and standard operating procedures.Patient Recruitment: Support patient recruitment and retention efforts.Training: Provide training and support to study staff on study protocols and procedures.Quality Assurance: Participate in quality control activities and internal audits.Qualifications and Skills:Education: Bachelor's degree in life sciences, nursing, or a related field.Experience: Fresher or recent graduate with a strong interest in clinical research.Knowledge: Basic understanding of clinical research principles and Good Clinical Practice (GCP).Skills: Excellent organizational, communication, and interpersonal skills.

Job Type- Fresher or Internship levelClinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe.Responsibilities:1. Assist in Protocol Development:Collaborate with the clinical research team to contribute to the development and review of clinical trial protocols.2. Site Identification and Selection:Participate in the process of identifying and selecting clinical trial sites by conducting feasibility assessments.3. Regulatory Compliance:Support the team in ensuring regulatory compliance throughout the clinical trial process.Assist in the preparation and submission of regulatory documents to appropriate health authorities.4. Site Initiation:Assist in the initiation of clinical trial sites by coordinating site training activities and ensuring that all necessary documentation is in place.5. Monitoring and Data Collection:Work closely with clinical research associates and investigators to monitor and collect data during the clinical trial.Assist in ensuring data accuracy, completeness, and adherence to protocol.6. Adverse Event Reporting:Contribute to the process of monitoring and reporting adverse events, ensuring compliance with regulatory requirements.7. Study Close-Out:Participate in the close-out activities of clinical trials, including the collection of essential documents and finalizing study reports.8. Collaboration and Communication:Work collaboratively with cross-functional teams, including clinical operations, data management, and regulatory affairs.Communicate effectively with investigators, site staff, and study sponsors.9. Documentation and Record Keeping:Maintain accurate and up-to-date documentation of all activities performed during the internship.Contribute to the development and organization of the trial master file.10. Learning and Development:Actively engage in learning opportunities provided during the internship to enhance knowledge of clinical research processes and industry regulations.Qualifications:Currently enrolled in a Bachelor's or Master's degree program in a related field (e.g., Life Sciences, Pharmacy, Nursing, etc.).Excellent communication and interpersonal skills.Detail-oriented with strong organizational and time management abilities.Ability to work independently and as part of a team.

We are seeking a highly motivated and compassionate recent graduate to join our clinical team as an Entry-Level Clinical Assistant/Clinical Associate. This is an excellent opportunity to gain hands-on experience in a clinical setting and contribute to patient care or clinical research. You will work closely with physicians, nurses, and other clinical staff, assisting with various tasks related to patient care, data collection, and administrative support. This role is ideal for individuals with a strong interest in healthcare and a desire to learn and grow in a dynamic environment.Responsibilities:Patient Care Support: Assist with patient intake and vital sign measurements.Prepare examination rooms and ensure they are clean and stocked with supplies.Provide basic patient support and comfort.Assist with the administration of basic medical procedures under supervision.Clinical Data Management: Accurately collect and record patient data in electronic health records (EHR) or clinical research databases.Assist in the preparation of clinical reports and data summaries.Maintain accurate and organized clinical records.Ensure data integrity and confidentiality.Administrative Support: Schedule patient appointments and manage patient flow.Answer phone calls and respond to patient inquiries.Assist with filing, photocopying, and other administrative tasks.Maintain inventory of clinical supplies.Clinical Research Support (if applicable): Assist with the recruitment and screening of clinical trial participants.Assist in the administration of study procedures and data collection.Maintain study documentation and regulatory files.Ensure adherence to study protocols and ethical guidelines.General Support: Assist clinical staff as needed.Participate in team meetings and training sessions.Maintain a clean and organized work environment.Any other duties as assigned.Qualifications:Bachelor's degree in a Life Science, Healthcare, or related field (e.g., Biology, Nursing, Psychology, Public Health).Strong interest in patient care or clinical research.Excellent communication and interpersonal skills.Strong attention to detail and accuracy.Ability to work independently and as part of a team. Strong organizational and time-management skills.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Must be a recent graduate.

We are seeking a highly motivated and enthusiastic recent graduate to join our team as a Life Science/Research Assistant. This is an excellent entry-level opportunity for individuals looking to gain hands-on experience in a dynamic research environment. You will work closely with senior researchers and contribute to ongoing projects by performing various laboratory tasks and data analysis. This role is perfect for someone passionate about life sciences and eager to learn and grow.Responsibilities:Laboratory Support: Prepare and maintain laboratory equipment and supplies.Assist in the preparation of reagents and solutions.Perform basic laboratory techniques such as pipetting, centrifugation, and gel electrophoresis.Maintain accurate and detailed laboratory records.Adhere to all safety protocols and laboratory procedures.Data Management: Assist in the collection and organization of research data.Perform basic data entry and analysis using software such as Microsoft Excel.Maintain data integrity and confidentiality.Research Assistance: Assist senior researchers in conducting experiments and studies.Follow established protocols and procedures.Observe and document experimental results.Assist in literature searches and data compilation.General Support: Maintain a clean and organized laboratory workspace.Assist with inventory management.Participate in team meetings and discussions.Any other duties as assigned.Qualifications:Bachelor's degree in Biology, Biochemistry, Biotechnology, or a related Life Science field.Strong interest in scientific research and laboratory work.Basic understanding of laboratory techniques and procedures.Excellent organizational and time-management skills.Ability to follow instructions and work independently as well as part of a team.Strong attention to detail and accuracy.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). Good communication skills.Must be a recent graduate.

Role & responsibilities:Outline the day-to-day responsibilities for this role.Preferred candidate profile:Specify required role expertise, previous job experience, or relevant certifications.Perks and benefits:Mention available facilities and benefits the company is offering with this job.

LLRI is seeking a motivated and detail-oriented Medical Records Coordinator to join our team. This entry-level position is ideal for recent graduates or individuals looking to begin a career in the healthcare administration field. The Medical Records Coordinator will be responsible for managing and organizing patient medical records, ensuring accuracy, confidentiality, and compliance withall relevant regulations. This role provides an excellent opportunity to gain hands-on experience in a fast-paced healthcare environment. Responsibilities:Record Management: Organize and maintain patient medical records, both electronic and physical, in accordance with established policies and procedures.Ensure accurate and timely filing, retrieval, and storage of medical records.Maintain confidentiality of patient information in compliance with HIPAA and other applicable regulations.Data Entry and Processing: Accurately input patient data into electronic health record (EHR) systems.Process requests for medical records from authorized personnel, including healthcare providers, insurance companies, and patients.Scan, index, and archive medical documents.Record Auditing and Quality Control: Review medical records for completeness and accuracy.Identify and resolve discrepancies or missing information in patient records.Assist in audits of medical records to ensure compliance with regulatory standards.Communication and Collaboration: Respond to inquiries from healthcare providers, staff, and patients regarding medical records.Collaborate with other departments to ensure smooth flow of information.Maintain professional and courteous communication with all stakeholders.Administrative Support: Assist with general administrative tasks, such as answering phones, scheduling appointments, and managing correspondence.Maintain and order office supplies related to record keeping.Perform other duties as assigned.Qualifications:Bachelor's degree or associates degree in healthcare administration, life sciences, or a related field (preferred).Basic understanding of medical terminology (a plus).Proficiency in computer applications, including Microsoft Office Suite and EHR systems.Excellent organizational and time-management skills.Strong attention to detail and accuracy.Ability to maintain confidentiality and handle sensitive information. Effective communication and interpersonal skills.Ability to learn quickly, and adapt to a fast paced environment.

Seeking a detail-oriented and enthusiastic Medical Billing Assistant to join our team. This entry-level position is perfect for recent graduates or individuals looking to start a career in healthcare billing. The Medical Billing Assistant will support the billing department by accurately processing claims, verifying patient insurance information, and assisting with various billing-related tasks. This role provides an excellent opportunity to learn the fundamentals of medical billing in a supportive environment.Responsibilities:Claim Processing: Prepare and submit electronic and paper insurance claims accurately and efficiently.Review claims for completeness and accuracy before submission.Follow up on submitted claims to ensure timely payment.Identify and resolve claim rejections and denials.Insurance Verification: Verify patient insurance coverage and eligibility.Contact insurance companies to obtain necessary information.Update patient insurance information in billing systems.Data Entry and Record Keeping: Accurately enter patient demographic and billing information into billing software.Maintain organized and up-to-date billing records.Scan and index billing documents.Payment Posting: Post payments from insurance companies and patients accurately.Reconcile payments with billing records.Identify and resolve payment discrepancies.Customer Service: Respond to patient inquiries regarding billing statements and insurance claims.Provide clear and accurate information to patients.Maintain professional and courteous communication with patients and insurance representatives.Administrative Support: Assist with general administrative tasks, such as filing, photocopying, and answering phones.Assist the billing department with special projects as needed.Qualifications:Associates or Bachelor’s degree in healthcare administration, business administration, or a related field (preferred).Basic understanding of medical billing terminology (a plus).Proficiency in computer applications, including Microsoft Office Suite.Strong attention to detail and accuracy.Excellent organizational and time-management skills.Ability to maintain confidentiality and handle sensitive information. Effective communication and interpersonal skills. Ability to learn quickly and adapt to changing environments.Preferred Skills:Knowledge of medical billing software and electronic health record (EHR) systems.Familiarity with HIPAA regulations.Any experience in a medical office or billing environment.