52 Medical Monitoring Jobs - Page 2

Roles and Responsibility Monitor medical enquiries and respond to customer inquiries professionally. Provide excellent customer service and ensure high customer satisfaction. Collaborate with internal teams to resolve medical queries and concerns. Develop and maintain knowledge of medical products and services. Analyze customer feedback and suggest improvements. Maintain accurate records of customer interactions and transactions. Job Requirements Strong communication and interpersonal skills are essential. Ability to work in a fast-paced environment and meet deadlines. Excellent problem-solving and analytical skills are required. Strong attention to detail and organizational skills are neces...

Roles and Responsibility Develop and implement effective monitoring strategies to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and mitigate potential risks and issues. Conduct thorough reviews of clinical trial data to ensure accuracy and completeness. Provide expert guidance on medical aspects of clinical development projects. Ensure timely and effective communication with stakeholders regarding project progress and updates. Identify areas for process improvement and implement changes to increase efficiency. Job Requirements Strong understanding of clinical development principles and regulations. Excellent analytical and problem-solving...

Eligibility Criteria: • MBBS graduates only from Indian institutes • Must hold a valid Medical Registration Certificate • Freshers & Experienced candidates are welcome Location: Miyapur, Hyderabad Hyderabad Role: Medical Monitor Work Mode: WFO (Full Time) Responsibilities: Provide protocol and therapeutic area training to study teams (both internal and external). Provide response to PI/site/EC queries. Prepare medical monitoring plan Review of Protocol deviation and Categorization of the same. CSR/SMP/SAP review Review study enrolled subject reports for eligibility in coordination with Project Manager/Designee, if required. SAE management if any, follow up with sites/ investigator for SAE up...

We are seeking a Clinical Business Analyst to support the enhancement and expansion of Clinical Data Review (CDR) dashboards . This role requires strong collaboration with client stakeholders, development teams, and analytics experts to drive the design and implementation of advanced dashboards for medical monitoring, protocol compliance, trial safety analytics, and regulatory reporting . The successful candidate will lead requirement gathering, user story creation, testing, and implementation support , ensuring alignment with clinical operations, biometrics, and regulatory expectations . Key Responsibilities: Client Collaboration Engage with client stakeholders (data managers, medical monit...

Role & responsibilities : Provide medical oversight and support for clinical trials, including the review of study protocols and medical documents. Act as a subject matter expert for clinical trial design, execution, and interpretation of clinical data. Evaluate and manage adverse event reporting, ensuring compliance with regulatory requirements. Conduct medical assessments and offer guidance on patient safety, recruitment strategies, and eligibility criteria. Collaborate with clinical operations, regulatory affairs, and data management teams to ensure smooth trial progression. Develop protocol, informed consent documents, Diary Card, Source Documents, Case Report form, Study Logs, Clinical ...

Key Responsibilities: Manage general medicine OPD and inpatient cases Conduct daily patient rounds and assist in treatment planning Ha ndle medical emergencies and coordinate with ICU teams Maintain accurate patient records and documentation Participate in academic and clinical discussions. Consultation with the patients and about his medical history. Examining the patient medical record histories. Fresher candidates preffered.

Working with Us Challenging. Meaningful. Life-changing. Those aren&apost words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You&aposll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We o...

As a Medical Monitor, you will be responsible for overseeing the medical aspects of in-house clinical trials and managing the CRO's medical monitoring for outsourced projects. Your duties will include developing and reviewing various clinical documents such as protocols, investigator's brochures, case record forms, product rationales, prescribing information, and drug interactions. You will also be tasked with organizing materials for Subject Expert Committee (SEC) meetings and actively participating in these meetings to support clinical trials and marketing approvals. In addition to the primary responsibilities, you will be involved in the medical review of Individual Case Safety Reports (I...

About The Role Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcom...

As a Clinical Data Services - Clinical Data Management professional at Accenture, you will be designated as a Clinical Data Svs Sr Analyst. With a Bachelor of Pharmacy or Master of Pharmacy qualification and 5 to 8 years of experience, you will play a crucial role in the Life Sciences R&D vertical. This vertical covers a wide range of services in the life sciences sector, including research laboratories, clinical trials support, regulatory services, pharmacovigilance, and patient services solutions. Your primary focus will be on Clinical Data Management, where you will be responsible for the collection, integration, and availability of data at appropriate quality and cost. This involves acti...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by convergin...

Responsibilities: Prepare clinical study reports, protocols & newsletters Design medical affairs strategies Conduct literature reviews & ICH compliance checks Write scientific documents with CRF & KOL input Protocols, abstracts, posters, manuscripts Provident fund

Novo Nordisk Global Business Services (GBS), India Department- Centralised Monitoring Unit (CMU)- Bangalore Does your motivation come from challenges and working in a dynamic environmentDo you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essentialDo you have a can-do attitude with continuous improvement as one of your career objectivesThen we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Global Trial Portfolio area. It is a perfect blend of skilled medical profession...

Novo Nordisk Global Business Services (GBS), India Department- Centralised Monitoring Unit (CMU)- Bangalore Does your motivation come from challenges and working in a dynamic environmentDo you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essentialDo you have a can-do attitude with continuous improvement as one of your career objectivesThen we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Global Trial Portfolio area. It is a perfect blend of skilled medical profession...

The Associate Medical Reviewer position at Novo Nordisk Global Business Solutions (GBS) India, specifically in the Centralised Monitoring Unit (CMU) department in Bangalore, Karnataka, IN, offers a challenging and dynamic environment for individuals who are motivated by working closely with key stakeholders and strive for continuous improvement in their career objectives. As an Associate Medical Reviewer, you will play a crucial role in conducting comprehensive medical reviews of clinical trial data across various therapy areas within the drug development portfolio. Your responsibilities will include ensuring the highest quality and consistency of medical data, with a strong emphasis on pati...

Registered Nurse Responsibilities: Maintaining accurate, complete health care records and reports. Administering medications to patients and monitoring them for side effects and reactions. Prescribing assistive medical devices and related treatments. Recording patient vital signs and medical information. Ordering medical diagnostic and clinical tests. Monitoring, reporting, and recording symptoms or changes in patient conditions. Administering non-intravenous medications. Assessing, implementing, planning, or evaluating patient nursing care plans by working with healthcare team members. Modifying patient health treatment plans as indicated by patient conditions and responses To apply submit ...

*Greetings From You & I Consulting ! You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. *Hurry Do Not Miss This Opportunity To Work For Global Giant MNC. We are hiring for the below locations under Medical Reviewer Role!! *Open Locations :- * Gandhinagar / Mumbai *Mode Of Interview - Virtual *Mode Of Work :- Work From Office * CTC Upto - 10 To 24Lpa *Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app) or email your CV to puja@careersuni.com PFB Job Insights for Medical Reviewer Role!! Author a CCC for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directl...

Novo Nordisk Global Business Solutions (GBS) India Department – Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environmentDo you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essentialDo you have a can-do attitude with continuous improvement as one of your career objectivesThen we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Me...

Novo Nordisk Global Business Solutions (GBS) India Department – Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environmentDo you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essentialDo you have a can-do attitude with continuous improvement as one of your career objectivesThen we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Me...

Novo Nordisk Global Business Solutions (GBS) India Department – Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environmentDo you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essentialDo you have a can-do attitude with continuous improvement as one of your career objectivesThen we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Me...

*Greetings From You & I Consulting ! You & I Consulting has always been in the spotlight for getting placed in 64+ MNC's PAN India. *Hurry Do Not Miss This Opportunity To Work For Global Giant MNC. We are hiring for the below locations under Medical Reviewer Role!! *Open Locations :- * Pune/ / Chennai / Mumbai *Mode Of Interview - Virtual *Mode Of Work :- Work From Office * CTC Upto - 10 To 24Lpa *Call Now our HR Specialist:- @ puja - 8250242229 (call or whts app) or email your CV to puja@careersuni.com PFB Job Insights for Medical Reviewer Role!! Author a CCC for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, dir...

Minimum 1 year experience in respective field Share the cv to recruitment@meditrinahospital.com 7736485552

Job description Remote & Full-time Opportunity for professionals with direct experience of min 2 years in disclosures. Job Description Summary The Clinical Trials Disclosure Specialist II position is responsible for the overall coordination and development of multiple disclosures deliverables, including but not limited to compliant registry authoring and maintenance of information on public registries, document redaction, and/or plain language authoring, ensuring adherence to relevant industry guidelines and client styles and formatting in accordance with all agreed upon timelines. Job Description Essential Functions: Independently performs/coordinates all activities for registration, mainte...

Department-Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Fun...

Position Overview: We are seeking a highly experienced and visionary Medical Director to lead and oversee all medical and clinical initiatives within the organization. This role is pivotal in ensuring the medical and scientific integrity of our programs, providing strategic direction, and driving excellence across research, clinical operations, and stakeholder engagement. The ideal candidate will bring deep clinical expertise, strong leadership capabilities, and a passion for advancing healthcare outcomes through evidence-based practices and innovative solutions. Key Responsibilities: Provide strategic medical leadership across all research, clinical, and operational activities. Oversee the ...