About the job About Us: MS Clinical Research Pvt Ltd (MSCR) is a pioneering clinical research organization committed to advancing healthcare and life sciences through innovative research and collaborations. We are expanding our team and are seeking motivated individuals to help us grow our business footprint. Job Summary: We are seeking a proactive and organized Front Office Associate to support the management of clinical study volunteers and ensure smooth front desk and administrative operations. The ideal candidate will have strong communication skills, attention to detail, and a customer-centric approach. This role involves active interaction with volunteers, including recruitment, coordination, and engagement. Experience with CRM systems is a plus. Key Responsibilities: Recruit and onboard new volunteers for clinical trials as per study requirements. Maintain and update the subject/volunteer database with accuracy and confidentiality. Interact with volunteers throughout the study cycle to ensure a positive experience. Handle phone calls, emails, and queries related to clinical tests. Coordinate with internal teams to manage appointment schedules and study timelines. Ensure proper documentation, data entry, and record-keeping for all volunteers. Manage front desk operations, including visitor handling and basic administrative tasks. Assist in preparing reports and maintain the confidentiality of volunteer data. Operate, handle, and maintain instruments as per SOPs and user manuals. Document instrument usage and ensure timely calibration with appropriate records. Support floor coordination for ongoing study activities. Schedule volunteer visits and follow up to ensure compliance and attendance. Promptly report any anomalies or concerns to the line manager and follow up until resolution or escalation. Key Requirements: Bachelor’s degree or equivalent experience in administration, life sciences, or front office roles. Strong proficiency in MS Office (Excel, Word, Outlook, PowerPoint) and general computer skills. Excellent communication, interpersonal, and coordination skills.
About the job About Us: MS Clinical Research Pvt Ltd (MSCR) is a pioneering clinical research organization committed to advancing healthcare and life sciences through innovative research and collaborations. We are expanding our team and are seeking motivated individuals to help us grow our business footprint. Job Summary: We are seeking a proactive and organized Front Office Associate to support the management of clinical study volunteers and ensure smooth front desk and administrative operations. The ideal candidate will have strong communication skills, attention to detail, and a customer-centric approach. This role involves active interaction with volunteers, including recruitment, coordination, and engagement. Experience with CRM systems is a plus. Key Responsibilities: Recruit and onboard new volunteers for clinical trials as per study requirements. Maintain and update the subject/volunteer database with accuracy and confidentiality. Interact with volunteers throughout the study cycle to ensure a positive experience. Handle phone calls, emails, and queries related to clinical tests. Coordinate with internal teams to manage appointment schedules and study timelines. Ensure proper documentation, data entry, and record-keeping for all volunteers. Manage front desk operations, including visitor handling and basic administrative tasks. Assist in preparing reports and maintain the confidentiality of volunteer data. Operate, handle, and maintain instruments as per SOPs and user manuals. Document instrument usage and ensure timely calibration with appropriate records. Support floor coordination for ongoing study activities. Schedule volunteer visits and follow up to ensure compliance and attendance. Promptly report any anomalies or concerns to the line manager and follow up until resolution or escalation. Key Requirements: Bachelor’s degree or equivalent experience in administration, life sciences, or front office roles. Strong proficiency in MS Office (Excel, Word, Outlook, PowerPoint) and general computer skills. Excellent communication, interpersonal, and coordination skills.
About the job Position Title: MBBS Doctor Department: Medical Experience: 0-1 year Location: Bengaluru Job Summary: We are seeking a dedicated and professional MBBS Doctor to join our team. The primary responsibility of this role is to assist in medical examinations, sign and verify medical reports, and ensure accurate documentation of patient information. The ideal candidate should have excellent clinical skills, a compassionate approach to patient care, and a keen eye for detail. Key Responsibilities: 1. Patient Care: Conduct thorough physical examinations and take detailed patient histories. Diagnose and treat common medical conditions. Prescribe medications and treatments as necessary. Provide patient education and counseling on health maintenance and disease prevention. 2. Medical Reports: Review, check, and sign off on medical reports, lab results, and diagnostic tests. Ensure all reports are accurate, complete, and properly documented. Communicate effectively with other healthcare professionals regarding patient care and reports. 3. Clinical Procedures: Assist in minor surgical procedures and emergency care as needed. Perform routine medical procedures such as injections, dressings, and suturing. 4. Documentation: Maintain detailed and accurate patient records. Ensure compliance with all regulatory and hospital policies regarding medical documentation. Participate in audits and reviews of patient records and medical reports. 5. Collaboration: Work collaboratively with other doctors, nurses, and healthcare staff. Participate in multidisciplinary team meetings and case discussions. Refer patients to specialists when necessary. 6. Continuing Education: Stay updated with the latest medical research, treatments, and technologies. Participate in ongoing training and professional development activities. 7. Ethical and Professional Conduct: Adhere to all ethical standards and guidelines set by the medical profession. Maintain patient confidentiality and uphold patient rights. Demonstrate professionalism in all interactions with patients and staff. Qualifications: MBBS degree from a recognized medical school. Valid medical license to practice. Experience: Previous experience or internship in a clinical setting is preferred but not mandatory. Fresh graduates are encouraged to apply. Skills: Strong clinical and diagnostic skills. Excellent communication and interpersonal skills. Attention to detail and strong organizational skills. Ability to work under pressure and handle multiple tasks simultaneously.
Job Role: Histology Cryo-toming Technician Location: Indiranagar, Bangalore Experience: 2-5 years Role Overview: We are seeking an experienced Histology Cryo-toming Technician who will be actively performing cryo-sectioning and histology procedures while also assisting in the setup, organization, and operationalization of a new histology laboratory. This is an exciting opportunity to contribute to building a state-of-the-art facility from the ground up. Key Responsibilities: Support in planning and setting up the histology laboratory , including equipment installation, workflow layout, and process optimization. Recommend necessary equipment, consumables, and reagents for cryo-sectioning and histology procedures. Establish and document standard operating procedures (SOPs) for frozen tissue processing, cryotomy, staining, and slide preparation. Perform cryotomy (sectioning frozen tissue samples) with precision and consistency. Embed tissue specimens in optimal cutting temperature (OCT) compound for cryo-sectioning. Perform routine and special staining as required for research or diagnostic use. Maintain cryostat and other lab equipment, ensuring calibration, cleanliness, and functionality. Label, organize, and archive tissue samples and slides accurately. Ensure compliance with GLP, biosafety standards, and laboratory quality protocols. Maintain proper records of specimens processed, slides prepared, and lab activities. Assist researchers and pathologists in preparing high-quality tissue sections for studies and analysis. Qualifications & Requirements: Diploma/Bachelor’s degree in Medical Laboratory Technology, Biomedical Sciences, Histotechnology, or related field. 2–5 years of experience in histology laboratory work, including cryo-sectioning (cryotomy) and staining. Prior exposure to setting up or organizing laboratory workflows is highly desirable. Knowledge of tissue processing, embedding (frozen and paraffin), microtomy, and staining techniques. Familiarity with cryostat operation and basic troubleshooting/maintenance. Strong understanding of laboratory safety and quality management systems. Excellent organizational skills, attention to detail, and ability to work independently. Key Skills: Proficiency in cryostat operation and frozen sectioning techniques Knowledge of histology workflow setup and optimization Strong documentation and SOP preparation skills Attention to detail and precision in handling delicate tissue specimens Ability to manage multiple responsibilities in a new lab environment
Role Overview We are seeking a Skin and Hair Sampling Technician to perform accurate sample collection, labeling, and storage from various test sites while ensuring strict adherence to SOPs, safety, and GLP standards. The role involves operating and maintaining lab instruments, documenting findings, assisting in report generation, and coordinating with the microbiology team for timely sample processing. Key Responsibilities: Perform sampling from various test sites (e.g., human skin and hair) following SOPs and safety guidelines. Handle sampling and related microbiological techniques. Record, label, and store samples accurately to maintain traceability. Operate and maintain lab instruments such as incubators, laminar flow hoods, and colony counters. Follow GLP (Good Laboratory Practice) and ensure aseptic procedures are strictly observed. Document findings clearly and maintain accurate laboratory records and logbooks. Support the team in report generation, including observation summaries and microbial count data. Assist in periodic calibration and cleaning of instruments used in sampling and testing. Coordinate with the microbiology team to ensure timely processing of samples. Qualifications: Diploma / Bachelor's degree in Medical Laboratory Technology (DMLT / BMLT) or relevant field. 1–2 years of lab experience, preferably in clinical research or microbiology. Familiarity with surface microbiological sampling is an added advantage. Good communication and team collaboration skills. Willingness to learn and adhere to protocols and documentation standards.
Job Role: Microbiologist Location: Indiranagar, Bangalore Experience: Fresher Job Overview: We are seeking a detail-oriented and enthusiastic Microbiologist (Fresher) to join our laboratory team. The role involves assisting in microbiological studies, performing experiments, and ensuring accurate documentation while adhering to safety and quality standards. This is an excellent opportunity for a recent graduate looking to build a strong foundation in microbiology within a professional research and testing environment. Key Responsibilities: Prepare study protocols in line with applicable SOPs and relevant guidelines. Conduct microbiological experiments as per established protocols and safety norms. Receive, handle, and process materials according to defined procedures. Isolate, maintain, and test microbial cultures with precision. Perform microbial sampling from various test sites (e.g., human skin and hair), ensuring adherence to SOPs and biosafety standards. Handle and execute microbiological techniques, including plating, swabbing, and dilutions. Record, label, and store samples accurately to ensure traceability and data integrity. Operate and maintain laboratory equipment such as incubators, laminar flow hoods, and colony counters. Follow Good Laboratory Practice (GLP) and ensure aseptic techniques are consistently observed. Maintain clean, well-organized lab spaces and participate in routine disinfection procedures. Document observations clearly and maintain up-to-date logbooks and laboratory records. Conduct internal quality control tests and escalate deviations to the Laboratory Director. Assist in the preparation of reports, including microbial count data and study summaries. Ensure periodic calibration and maintenance of instruments used in sampling and testing. Coordinate with internal teams to ensure timely processing of samples and project deliverables. Engage professionally with colleagues, clients, and external stakeholders. Undertake any additional duties assigned by the Laboratory Director. Qualifications & Requirements: Fresher MSc Biotechnology/Microbiology/ Biochemistry Strong documentation and SOP preparation skills Attention to detail and precision in handling delicate tissue specimens Ability to manage multiple responsibilities in a new lab environment
About the job Job Title: Medical Writer Company: MS Clinical Research Pvt Ltd Location: Indiranagar, Bangalore Job Type: Full-time Experience: 2-4 years About MS Clinical : MS Clinical is a dynamic and innovative company dedicated to advancing medical research and improving patient outcomes. We specialize in conducting clinical trials and providing comprehensive medical writing services to pharmaceutical, biotechnology, and healthcare organizations worldwide. Job Description : We are seeking an experienced Medical Writer to join our vibrant team. The successful candidate will be responsible for creating high-quality, scientifically accurate medical documents in support of our clinical trial activities and regulatory submissions. The ideal candidate will have a strong background in medical writing, excellent communication skills, and the ability to work both independently and collaboratively in a fast-paced environment. Responsibilities : Prepare and review clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and other clinical trial documents in accordance with regulatory guidelines and industry standards. Collaborate with cross-functional teams, including clinical operations, regulatory affairs, and biostatistics, to ensure the accuracy and completeness of medical writing deliverables. Interpret and summarize clinical trial data from various sources, including study reports, statistical analyses, and scientific literature. Assist in the preparation of regulatory submissions, including INDs, NDAs, BLAs, and MAAs, by providing high-quality medical writing support. Participate in project meetings, provide updates on the status of medical writing activities, and contribute to project planning and timelines. Stay current with developments in the field of medical writing, regulatory requirements, and therapeutic areas relevant to our projects. Mentor junior medical writers and provide guidance on best practices for medical writing and document preparation. Qualifications : Bachelor's degree in life sciences, pharmacy, or related field; advanced degree (e.g., MD, PhD, PharmD) preferred. Minimum of 3 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry. Proficiency in interpreting and summarizing clinical trial data, including statistical analyses and safety reports. Strong understanding of regulatory guidelines (e.g., ICH, FDA, EMA) governing the preparation of clinical trial documents and regulatory submissions. Excellent written and verbal communication skills, with the ability to communicate complex scientific concepts clearly and effectively. Detail-oriented with exceptional organizational and time management skills. Ability to work independently and collaboratively in a multidisciplinary team environment. Proficiency in Microsoft Office Suite and familiarity with document management systems (e.g., SharePoint). Benefits : MS Clinical offers a competitive salary and benefits package, including health insurance, retirement plans, and opportunities for professional development and advancement.
Job Title : Clinical Research Associate (CRA) Experience: Minimum 3 years Company : MS Clinical Research Pvt Ltd About Us: MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical solutions. Job Summary : We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory requirements, and excellent communication and organizational skills. Key Responsibilities : Site Management: Conduct site initiation, routine monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory requirements. Build and maintain strong relationships with investigative sites, investigators, and study coordinators. Clinical Trial Monitoring: Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance. Ensure timely resolution of data queries and issues identified during monitoring visits. Protocol Compliance: Ensure that all study activities are conducted in accordance with the approved protocol, SOPs, and applicable regulatory guidelines. Collaborate with investigators to address and resolve protocol-related queries. Regulatory Compliance: Assist in the preparation and submission of regulatory documents to ethics committees and regulatory authorities. Stay informed about changes in regulatory requirements and update study teams accordingly. Data Management: Collaborate with data management teams to ensure accurate and timely data collection and entry. Perform source data verification and data validation activities. Safety Reporting: Monitor and report adverse events in compliance with regulatory requirements and safety reporting procedures. Ensure that safety reports are submitted to relevant authorities and stakeholders. Training and Support: Provide training and support to site staff on study protocols, data collection, and regulatory compliance. Act as a resource for investigators and site staff throughout the duration of the study. Requirements : Education: Bachelor's degree in a relevant life sciences field. Experience : Minimum of 3 years of experience as a Clinical Research Associate. Proven track record of successful site management and monitoring in clinical trials. Regulatory Knowledge: Familiarity with regulatory requirements and guidelines governing clinical trials. Communication Skills: Excellent verbal and written communication skills. Organizational Skills: Strong organizational and time management skills with attention to detail. Team Collaboration: Ability to work effectively in cross-functional teams and independently. Travel: Willingness to travel to investigative sites as needed. Benefits: Competitive salary and benefits package. Opportunities for professional development and advancement. Collaborative and dynamic work environment. Join our team at MS Clinical Research and contribute to the advancement of clinical research and the development of innovative healthcare solutions.
About the job Job Title: Molecular Biologist – qPCR Consultant (Preclinical – In Vitro) Location: MS Clinical Research Pvt Ltd (MSCR) Department: Preclinical – In Vitro Employment Type: Consultant/Part-time Experience: Minimum 10 years in Molecular Biology with hands-on expertise in qPCR Role Overview: MSCR is seeking an accomplished Molecular Biologist – qPCR Consultant to support our preclinical (in-vitro) research team. The ideal candidate will bring deep technical expertise in qPCR assay development, optimization, and data analysis, specifically aligned with preclinical drug screening and mechanistic in-vitro studies. This is a strategic consulting role aimed at enhancing our molecular biology capabilities in gene expression, target validation, and biomarker discovery. Key Responsibilities: Provide technical leadership in the design, development, and validation of qPCR assays for in-vitro studies including cytotoxicity, gene expression profiling, and pathway analysis. Advise on sample preparation, RNA/DNA extraction, and quality control specific to in-vitro systems. Guide the team in primer/probe design, assay optimization, and standard curve generation. Troubleshoot experimental issues and recommend improvements to protocols and workflows. Ensure robust data integrity, statistical soundness, and scientific documentation of qPCR results. Review experimental designs to align with regulatory and scientific requirements for GLP-compliant preclinical studies. Train lab scientists on best practices for qPCR technique and data interpretation. Collaborate with research scientists and study directors to integrate molecular endpoints in preclinical study design. Stay updated with emerging trends, technologies, and best practices in molecular biology and qPCR. Qualifications: Ph.D. or Master’s in Molecular Biology, Cell Biology, Biotechnology, or a related field. Minimum 10 years of hands-on experience in molecular biology techniques, with a strong focus on qPCR in preclinical models. Excellent analytical, documentation, and communication skills. Desirable Skills: Knowledge of cell-based assay systems, molecular endpoints, and biomarker quantification. Exposure to RT-qPCR, miRNA analysis, or multiplex PCR. Engagement Type & Compensation: Consulting basis – Part-time, Remote, Hybrid Remuneration commensurate with experience and scope of involvement.
Job Title: Trichologist Location: Indiranagar, Bangalore Employment Type: Part-time/Contract Job Overview We are seeking a qualified and experienced Trichologist to join our team. The ideal candidate will specialize in diagnosing and treating hair and scalp conditions, providing expert consultations, recommending appropriate treatments, and offering preventive care advice to clients. Key Responsibilities Conduct detailed consultations to assess hair and scalp health. Diagnose conditions such as hair thinning, hair loss (alopecia), dandruff, psoriasis, seborrheic dermatitis, and other scalp disorders. Recommend personalized treatment plans, products, and lifestyle modifications. Perform non-invasive treatments like scalp therapies, mesotherapy, PRP (if certified), and other clinical hair restoration procedures. Educate clients about hair care routines, diet, and stress management to improve hair health. Work closely with dermatologists, nutritionists, or other healthcare professionals when necessary. Maintain detailed patient records and treatment histories. Keep up-to-date with the latest advancements in trichology, hair restoration techniques, and scalp care products. Ensure compliance with hygiene, safety, and ethical standards in all procedures. Required Qualifications Certification/Diploma in Trichology or related field. Strong knowledge of hair and scalp physiology and pathology. Experience in a clinic, wellness center, or salon specializing in hair care is preferred. Good understanding of nutrition and its impact on hair health. Excellent communication and interpersonal skills. Ability to build trust and long-term relationships with clients. Preferred Skills Knowledge of advanced hair treatment technologies (e.g., laser therapy, PRP). Understanding of cosmetic hair care products and formulations. Ability to work with both medical and non-medical teams.
Job Title: Instrument Operator – Healthcare Department: Biomedical / Clinical Support Services Location: [MS Clinical Research Pvt Ltd, Cambridge layout] Reports To: Department Head Employment Type: Full-Time Job Summary: The Instrument Operator is responsible for the proper handling, operation, maintenance, and basic troubleshooting of medical and diagnostic instruments and equipment. This role ensures equipment is functioning safely, accurately, and efficiently to support high-quality. Key Responsibilities: Conduct trials as per the ICH GCP and Protocol Specified Guidelines. Operating, handling, and maintenance of instruments as per SOP and instrument manual Documenting the instrument data. Calibration of instruments within the timeline and maintaining records. Floor coordination for the study activities. Assisting in scheduling the subjects for the visits. Timely submission of study-related data for the analysis. In case of any concern or any anomaly, report to the line manager immediately and follow up until resolution/ escalation to management if required. Qualifications and Skills: Diploma or Certification in Medical Instrumentation Minimum 1 year of experience operating clinical instruments in a hospital Basic troubleshooting and maintenance knowledge. Good communication skills and attention to detail. Ability to work under pressure and follow strict protocols.
As a Lead Clinical Trial Participant Recruitment, you will be responsible for managing and overseeing all aspects of participant outreach, screening, scheduling, engagement, and follow-ups for ongoing and upcoming clinical studies. Your role will involve supervising the recruitment team, ensuring timely and ethical enrollment of subjects, and maintaining consistent communication throughout the trial journey. You will design and implement effective outreach strategies across digital platforms, local communities, and healthcare networks. Identifying and engaging eligible participants in line with study inclusion/exclusion criteria will be a key responsibility. Additionally, you will supervise the recruitment team to ensure consistent performance and quality in screening and outreach. Coordinating and managing screening appointments, enrollment visits, and follow-up schedules for participants will be part of your duties. Ensuring timely reminders and communication to reduce no-shows and improve retention, as well as maintaining updated participant logs and scheduling systems, will be crucial. You will serve as the primary point of contact for participants, providing clear, compassionate, and timely communication. Educating participants on trial protocols, procedures, timelines, and expectations will also be essential. Developing and implementing engagement strategies to enhance participant experience and retention throughout the study duration is another significant aspect of your role. Managing reimbursements and compensation disbursements in line with trial budgets and regulatory guidelines will also fall under your responsibilities. Leading, training, and mentoring the recruitment team to meet enrollment targets and maintain compliance, collaborating closely with clinical and operations teams, and monitoring recruitment performance to prepare regular reports for internal stakeholders are key components of your role. To qualify for this position, you should have a Bachelor's or Master's degree in Life Sciences, Healthcare, HR, Social Work, or a related field. A minimum of 5 years of experience in clinical trial recruitment or community outreach, with at least 2 years in a leadership or supervisory role, is required. A strong understanding of clinical research processes, ethical recruitment practices, and regulatory guidelines (GCP, ICH) is necessary. You should also have proven ability to recruit participants directly and manage a team effectively, along with basic knowledge of administrative coordination and facility management. Excellent communication, organizational, and interpersonal skills are essential, and experience with digital recruitment tools and social media outreach is preferred. Additionally, you should be able to work under tight timelines, multitask, and adapt to changing priorities.,
Job Title : Clinical Research Coordinator (minimum 1 year of experience) Company : MS Clinical Research Pvt Ltd About Us : MS Clinical Research (MSCR) is a dynamic and forward-thinking clinical research organization dedicated to conducting cutting-edge clinical trials. We are committed to advancing medical science and contributing to the development of innovative healthcare solutions. Job Summary: We are looking for enthusiastic and detail-oriented individuals to join our team as Clinical Research Coordinators. Only candidates with a minimum of 1-3 years of experience in BA/BE studies should apply. Key Responsibilities : 1. Study Coordination: Assist in the planning, initiation, and coordination of clinical trials under the supervision of the Principal Investigator and study team. Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. 2. Participant Recruitment and Screening: Identify and screen potential study participants. Coordinate participant recruitment activities and maintain accurate screening logs. 3. Informed Consent Process: Facilitate the informed consent process for study participants. Maintain documentation of informed consent and regulatory compliance. 4. Data Collection and Management: Collect and record study data accurately and in a timely manner. Ensure completeness and quality of data through routine checks and validations. 5. Site Management: Liaise with investigative sites and study teams to facilitate smooth study conduct. Assist in the preparation and submission of regulatory documents. 6. Safety Reporting: Monitor and report adverse events according to regulatory requirements. Collaborate with the study team to ensure the safety of participants. 7. Training and Development: Participate in training programs to develop a strong foundation in clinical research practices. Stay informed about relevant regulations and industry trends. Requirements: Education: Bachelor's degree in a relevant life sciences field. Skills and Qualities: Strong organizational and multitasking skills. Excellent communication and interpersonal skills. Detail-oriented with a commitment to accuracy. Team Collaboration: Ability to work effectively in a collaborative team environment. Commitment to Compliance: Understanding of ethical principles and a commitment to ensuring regulatory compliance. Learning Agility: Demonstrated ability and willingness to learn and adapt in a fast-paced environment. Benefits: Comprehensive training and mentorship program. Opportunities for professional growth and development. Competitive compensation and benefits package. Join our team at MS Clinical Research and embark on a rewarding career in clinical research. This is an excellent opportunity to contribute to the advancement of medical science and make a meaningful impact on healthcare research.
Job Title : Clinical Research Coordinator (minimum 1 year of experience) Company : MS Clinical Research Pvt Ltd About Us : MS Clinical Research (MSCR) is a dynamic and forward-thinking clinical research organization dedicated to conducting cutting-edge clinical trials. We are committed to advancing medical science and contributing to the development of innovative healthcare solutions. Job Summary: We are looking for enthusiastic and detail-oriented individuals to join our team as Clinical Research Coordinators. Only candidates with a minimum of 1-3 years of experience in BA/BE studies should apply. Key Responsibilities : 1. Study Coordination: Assist in the planning, initiation, and coordination of clinical trials under the supervision of the Principal Investigator and study team. Ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. 2. Participant Recruitment and Screening: Identify and screen potential study participants. Coordinate participant recruitment activities and maintain accurate screening logs. 3. Informed Consent Process: Facilitate the informed consent process for study participants. Maintain documentation of informed consent and regulatory compliance. 4. Data Collection and Management: Collect and record study data accurately and in a timely manner. Ensure completeness and quality of data through routine checks and validations. 5. Site Management: Liaise with investigative sites and study teams to facilitate smooth study conduct. Assist in the preparation and submission of regulatory documents. 6. Safety Reporting: Monitor and report adverse events according to regulatory requirements. Collaborate with the study team to ensure the safety of participants. 7. Training and Development: Participate in training programs to develop a strong foundation in clinical research practices. Stay informed about relevant regulations and industry trends. Requirements: Education: Bachelor's degree in a relevant life sciences field. Skills and Qualities: Strong organizational and multitasking skills. Excellent communication and interpersonal skills. Detail-oriented with a commitment to accuracy. Team Collaboration: Ability to work effectively in a collaborative team environment. Commitment to Compliance: Understanding of ethical principles and a commitment to ensuring regulatory compliance. Learning Agility: Demonstrated ability and willingness to learn and adapt in a fast-paced environment. Benefits: Comprehensive training and mentorship program. Opportunities for professional growth and development. Competitive compensation and benefits package. Join our team at MS Clinical Research and embark on a rewarding career in clinical research. This is an excellent opportunity to contribute to the advancement of medical science and make a meaningful impact on healthcare research.