Clinical Coordinator Jobs

We are looking for a Clinical Research Coordinator to join our team in Nagpur. The ideal candidate will have 1 to 3 years of experience in clinical research and hold a degree in B.Pharma, B.Sc, or an Advanced/Higher Diploma.**Key Responsibilities:**- **Facilitate Clinical Trials:** Coordinate all aspects of clinical studies, including patient recruitment, scheduling appointments, and managing trial documentation to ensure smooth operations.- **Data Collection and Management:** Gather and maintain accurate data throughout the study, ensuring compliance with regulatory standards and protocols.- **Collaboration with Investigators:** Work closely with physicians and investigators to support trial conduct, provide updates, and address any issues that arise during the study.- **Monitoring Adherence to Protocols:** Regularly review study procedures to ensure that all activities comply with protocol and regulatory requirements.- **Patient Interaction:** Communicate effectively with study participants, helping them understand the study processes and addressing any concerns they may have.**Required Skills and Expectations:**- Strong understanding of clinical research processes and regulatory guidelines is essential.- Excellent organizational skills and attention to detail to manage multiple tasks efficiently.- Ability to communicate clearly and effectively, both verbally and in writing, with team members and participants.- Proficiency in using data management software and tools related to clinical research.- A committed attitude towards enhancing patient safety and welfare throughout the research process. The ideal candidate will be proactive, dedicated, and passionate about contributing to medical advancements through clinical research.

Company: Venture SmarterLocation: RemoteSalary: $3,500 - $4,500 per month (based on experience)Job DescriptionVenture Smarter is looking for a detail-oriented and organized Data Coordinator to join our team. This remote position will involve managing and organizing large sets of data, ensuring accuracy, and helping streamline data processes across multiple projects. You'll play a key role in supporting our data-driven initiatives by maintaining databases and ensuring data quality.To Apply:Head on over to search on Google for Venture Smarter then go to our Career page from the homepage if you dare to aspire for better in your career!**** Given the high number of applications we receive, we will only respond to those who meet the qualifications for the positions applied for.Please note that we will not reply to job application inquiries sent to our social media accounts. All communication from us will be conducted via email.If you do not receive a response, you are welcome to re-apply after six months for another suitable position within our company. ****Venture Smarter has been featured in media outlets such as CBS News, Digital Journal, and Go Banking Rates. Check us out youll know were the place to be.Key ResponsibilitiesManage and update company databases to ensure accuracy and completeness.Analyze data for trends, inconsistencies, and actionable insights.Coordinate with different teams to collect, organize, and report data as needed.Assist in data entry, data cleansing, and the preparation of reports.Support the development and implementation of data collection procedures and systems.Collaborate with IT and other departments to improve data workflows and storage solutions.RequirementsProven experience in data coordination, data entry, or similar administrative roles.Strong attention to detail and the ability to identify data discrepancies.Proficiency in Microsoft Excel, Google Sheets, and data management software.Excellent communication skills to work with different teams and stakeholders.Ability to manage multiple tasks and meet deadlines in a remote work environment.BenefitsCompetitive monthly salary.Flexible work-from-home setup.Health and wellness benefits.Opportunities for career advancement.

Role OverviewThe Clinical Coordinator is responsible for guiding patients through their treatment journeyfrom initial consultation to conversion and follow-up. The role requires excellent communication, patient handling, and sales counselling skills to ensure a seamless experience and achieve clinic targets.Key Roles & Responsibilities1. Patient Consultation & Counselling Welcome clients warmly and conduct initial counselling sessions. Understand patient concerns, expectations, and medical history. Clearly explain available treatments (lasers, skin, hair, anti-aging, slimming, dental, etc.). Recommend treatment packages as per clinic protocols and patient needs. Ensure patients are well-informed about procedures, benefits, risks, and post-care.2. Sales & Conversion Achieve monthly counselling and sales targets. Follow up with leads and convert inquiries into bookings and registrations. Maintain a high conversion ratio through professional counselling and rapport-building. Promote ongoing offers, packages, and membership plans.3. Patient Experience Management Coordinate with doctors, therapists, and front desk for smooth patient flow. Ensure high standards of hospitality and patient satisfaction. Address queries and concerns promptly and professionally. Ensure proper consent forms are signed before procedures.4. Documentation & Reporting Update CRM/records with patient details, consultations, and follow-ups. Maintain accurate logs of conversions, revenue, and daily activity. Submit counselling and sales reports to management.5. Clinic Coordination Assist in managing appointments and treatment room readiness. Maintain strong communication with the medical team for smooth operations. Support camps, workshops, open houses, and promotional events.6. Professional Conduct & Grooming Maintain excellent grooming, body language, and communication. Follow clinic SOPs, confidentiality, and ethical standards. Represent the brand with professionalism and positivity.

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Key Responsibilities:1. Trial Architecture:> Contribute to the development of dynamic trial plans and protocols in tandem with the clinical operations team.> Collaborate on the strategic selection and qualification of investigative sites.2. Site Symphony:> Conduct harmonious site initiation, monitoring, and close-out visits to ensure seamless protocol execution and pristine data collection.> Cultivate collaborative relationships with investigative site teams, providing support and guidance.3. Regulatory Mastery:> Ensure meticulous adherence to regulatory standards, guidelines, and the principles of Good Clinical Practice (GCP).> Spearhead the preparation and submission of regulatory documents to ethics committees and regulatory authorities.4. Data Choreography:> Direct the orchestration of data collection, ensuring the accuracy and completeness of clinical trial data.> Collaborate with data management teams to resolve data discrepancies and maintain a symphony of data quality.5. Risk Ballet:> Proactively identify potential risks to trial success and choreograph mitigation strategies in collaboration with project teams.6. Communication Sonata:> Cultivate clear and resonant communication channels with internal and external stakeholders.> Compose eloquent and timely study progress reports, fostering transparency and accountability.Qualifications:Bachelor's or advanced degree in a relevant field (Life Sciences, Nursing, etc.).Demonstrated experience as a Clinical Research Associate, preferably in the pharmaceutical or biotechnology domain.Profound knowledge of clinical trial processes, regulatory requirements, and GCP.Exceptional interpersonal and communication finesse

Patient Care: Examine and diagnose patients presenting in the emergency department or admitted to the hospital.Develop and implement treatment plans in collaboration with specialists and senior medical staff.Clinical Rounds: Conduct regular clinical rounds to monitor the progress of admitted patients.Provide timely updates to the attending consultants and senior medical staff.Emergency Response: Respond promptly to medical emergencies and provide immediate care.Stabilize patients before transferring them to specialized units or higher levels of care.Medical Records: Maintain accurate and up-to-date medical records for all patients under your care.Document patient history, examination findings, treatment plans, and progress notes.Collaboration: Collaborate with consultants, nurses, and other healthcare professionals to ensure comprehensive patient care.Attend and actively participate in departmental meetings and case discussions.Patient Education: Communicate effectively with patients and their families, providing information about their medical condition, treatment plans, and post-discharge care.Quality Assurance:Adhere to medical and ethical standards, ensuring the delivery of quality healthcare services.Participate in quality improvement initiatives and audits.Quality Assurance ring: Provide guidance and mentorship to junior medical staff, interns, and medical students.Contribute to the training and development of the healthcare team.

Clinical Co-ordinator / Patient Co-ordinator - Female onlyExperience- 2 - 3 yrsJob DescriptionAssist to Doctor in OPDLineup Patient for Procedure, time & data.Coordinate with Patient and Doctor.Coordinate with Embryologist and clinical team.Update Reports to Patient.Conduct Patient CampsMaintain File of Patient (Manual+ Computer).Salary: INR 2,00,000 - 2,50,000 P.A.Industry:Medical / Healthcare / HospitalsFunctional Area:Medical , Healthcare , R&D , Pharmaceuticals , BiotechnologyRole Category:Medical ProfessionalRole:Medical OfficerEmployment Type:Permanent Job, Full TimeQualification :Preferably BHMS/BAMS. Other qualifications can also be considered (eg. Hospital Administration, Any Graduate, Any Post-Graduate)Desired Candidate ProfileGood experience in Patient/ Clinical Coordination.Preferably BHMS/BAMSGood communication skills Experience in Healthcare will be preferred

1. Conducting 4 CBT and ERP Session daily 2. Conduction training for mental health professional 3. Mass Awareness Activity through webinar, talk show, live video, social media creative posting 4. Leading research project 5. Documentation of base practicing6. Developing web content

Need fluency in English,Assessment childTaking session of childManage centreParents counseling

Position: Clinical Research CoordinatorQualification Bio Science (B.Pharm/Bio Tech etc.)Experience Above 1 Year (Clinical Research Experience must) Timing General ShiftSalary 2L 2.5L (Per annum)Location Visakhapatnam/Chennai/BangaloreLanguage Know English/Kannada/TeluguJOB Description Clinical Research Coordinator To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist Senior CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Coordinate between the local/Central laboratory and courier for the shipment. Assist the pharmacist in drug accountability and temperature maintaining logs. Assist the Sr. CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report Sr.DGM daily and take advice for further action.

manage documentation at the trial site and conduct patient visits.

Overseeing the trouble-free running of clinical trialsCollecting data obtained from research, coding and analyzing itManaging budgets set aside for researchCommunicating with participants regarding study objectivesAdministering questionnaires and monitoring participants to ensure they adhere to the studys rulesLiaising with laboratories regarding research findingsMonitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standardsMaintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelinesDirecting the collection, labeling, storage and transport of all specimensMaking sure that all equipment and supplies needed for the study are in-stock and in good working order

Position Clinical Research CoordinatorQualification B.PharmExperience - Above 1YearsTiming - General ShiftSalary Based upon PerformanceLocation ChennaiLicence: Pharmacy Lice(Only B. Pharm is eligible for this Job)Job Description Clinical Research Coordinator: To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist the Site Head in the managing the Site to ensure ethical conduct of research activities. Assist Site Head in evaluates protocols, policies and procedures regarding research projects and studies. Maintains pertinent records and documentation. Provide guidance to CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Oversight of Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Assist the pharmacist in drug accountability and temperature maintaining logs. Monitoring Sr. CRC and CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report to the Site Head daily and take advice for further action. Delegate the work to Senior/Junior/Trainee CRCs as per the requirement.Job Types: Full-time, PermanentSalary: ?10,000.00 - ?15,000.00 per month

We are looking for 100 Clinical SAS Programmer/ Biostatistician/ Clinical data coordinator Posts in Chennai with deep knowledge in Clinical SAS Programmer,Clinical Data Manager,Biostatistics and Required Educational Qualification is : Other Bachelor Degree

We are Hiring on urgent basis Sales Manager Noida Location Good salary and insensitive.