6710 Clinical Research Jobs - Page 46

Develop and implement effective aggregate reporting strategies to meet business objectives.Analyze complex data sets to identify trends,patterns, providing insights to stakeholders.Create comprehensive reports using various tools and technologies Required Candidate profile Minimum 2 years of experience in aggregate reporting or a related field.Strong understanding of employment firms and recruitment services.Excellent analytical and problem-solving skills.

Manage and oversee clinical study data management activities, ensuring compliance with regulatory requirements.Develop and implement effective data management plans to ensure data quality and integrity. Required Candidate profile Strong knowledge of clinical trial conduct, including GCP guidelines and regulatory requirements.Experience with data management systems, such as electronic data capture and database management.

Conduct thorough medical device safety assessments and evaluations.Develop and implement effective safety protocols and procedures.Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Strong knowledge of medical devices and their safety regulations.Excellent analytical and problem-solving skills.Ability to work effectively in a team environment.

Manage and maintain accurate clinical data records, ensuring compliance with regulatory requirements.Perform data reconciliation tasks to identify and resolve discrepancies in clinical trial data. Required Candidate profile Strong understanding of clinical data management principles and practices.Proficiency in data analysis and problem-solving skills with attention to detail.Excellent communication and collaboration

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Collaborate with cross-functional teams to ensure accurate /timely delivery of clinical data.Develop and implement data quality control process Required Candidate profile Strong knowledge of Veeva EDC and clinical data management principles.Excellent analytical and problem-solving skills with attention to detail.Ability to work effectively in a team environment

Conduct clinical trials to ensure compliance with regulatory requirements and company protocols.Collaborate with cross-functional teams to design, implement, and monitor study procedures.Develop and maintain relationships with investigators Required Candidate profile Strong knowledge of Good Clinical Practice (GCP) principles and regulations.Experience in conducting clinical trials from initiation to closeout.Excellent communication and interpersonal skills.

Analyze and interpret complex clinical trial data using SAS.Develop and maintain databases, spreadsheets, and reports using Veeva.Collaborate with cross-functional teams to ensure accurate and timely delivery of results. Required Candidate profile Strong proficiency in SAS programming language.Experience with Veeva database management system.Excellent analytical and problem-solving skills.Ability to work independently and as part of a team.

8 years experiences for RA role in medical device and or pharmaceutical industry.Good understanding for regulations and policies issued by India, US FDA and EU, and ability to interpret international regulatory requirements. Required Candidate profile Desired Skills:RA role in medical device, US FDA and EU. Bachelor degree in Medical, Mechanical, Electric Life Science or other healthcare related majors.

Supervisor, Coding Overview The Supervisor, Coding plays a crucial role in ensuring the accuracy and compliance of medical coding processes within a healthcare organization. This position involves overseeing and leading a team of medical coders, conducting quality assurance audits, providing feedback, and implementing improvement strategies to enhance coding accuracy and efficiency. Responsibilities Team Leadership: Lead and manage a team of medical coders. Provide guidance, support, and mentorship to coding staff. Foster a collaborative and positive work environment. Conduct regular team meetings to discuss updates, challenges, and training opportunities. Quality Assurance: Develop and impl...

Job Summary Coding Denial Supervisor to provide direction to a team of Coding Denial Specialists, who are responsible for working on assigned claim edits and rejection work queues. The Coding Denial Supervisor will ensure timely investigation and resolution of health plan denials. Additionally, the Coding Denial Supervisor will assist in determining appropriate actions and providing resolutions for health plan denials. Essential Functions and Tasks Ensuring the timely investigation and resolution of health plan denials Assist in Implementing and maintaining policies and procedures for denial management Providing training and support to the team members to enhance their skills and knowledge E...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 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 li...

Job Profile Quality Assurance, Quality Control, Clinical Research , Regulatory Affairs, Medical Record Summarization , Medical Claims , Medical Officer, Medical Billing , Pharmacist, ADL, ARD, FRD, CDM, Production, R&D , Lab Technician

We are looking for a skilled F&B and Event Service Expert with 2 to 6 years of experience to join our team at Le Mridien. The ideal candidate will have a strong background in the hospitality industry, particularly in hotels and restaurants. Roles and Responsibility Coordinate and manage food and beverage services for events and meetings. Develop and implement effective event service strategies to ensure high-quality service delivery. Collaborate with cross-functional teams to plan and execute successful events. Conduct site visits and inspections to ensure compliance with company standards. Train and mentor staff members on food safety protocols and customer service skills. Analyze event fee...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: BCom Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving customer id...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with AML and Fraud mgmt experience.Understand & implement laws, and regulations designed to stop the practice of generating income through illegal actions during transfer of funds. Anti Money Laundering law covers limited number of transactions and criminal behaviors to prevent terrorist financing an...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with AML and Fraud mgmt experience.Understand & implement laws, and regulations designed to stop the practice of generating income through illegal actions during transfer of funds. Anti Money Laundering law covers limited number of transactions and criminal behaviors to prevent terrorist financing an...

Conduct thorough medical reviews of patient records, including diagnoses,treatments, and test results.Analyze medical data to identify trends,areas for improvement.Collaborate with healthcare professionals to develop effective treatment plans. Required Candidate profile Strong knowledge of medical terminology, anatomy, and physiology. Ability to work effectively in a fast-paced environment with multiple priorities. Effective communication and interpersonal skills.

Accurately code medical records using relevant codes and guidelines.Ensure compliance with regulatory requirements and industry standards.Collaborate with healthcare professionals to clarify coding discrepancies. Required Candidate profile Strong knowledge of medical terminology and coding principles. Experience with electronic health records (EHR) systems. Familiarity with coding software and tools.

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 3 to 5 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...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services 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 l...

Publish regulatory submissions to relevant authorities, ensuring compliance with required standards.Coordinate with cross-functional teams to ensure timely submission of regulatory documents. Required Candidate profile Strong understanding of regulatory requirements and guidelines governing submissions. Excellent publishing skills, including attention to detail and ability to meet deadlines.

Conduct thorough medical reviews of device-related documents to ensure compliance with regulatory requirements.Collaborate with cross-functional teams to identify and resolve issues related to medical documentation. Required Candidate profile Familiarity with electronic health records (EHRs) and other healthcare software systems. Strong organizational skills with the ability to prioritize tasks and manage multiple projects simultaneously.

Collaborate with internal stakeholders to resolve issues related to regulatory submissions.Stay updated with changes in regulatory requirements and implement necessary updates to publishing processes. Required Candidate profile Experience in regulatory submissions publishing, preferably in the employment or recruitment industry. Strong understanding of regulatory requirements and guidelines governing submissions.

Conduct thorough medical reviews of device-related documents to ensure compliance with regulatory requirements.Collaborate with cross-functional teams to identify and resolve issues related to device safety and efficacy. Required Candidate profile Strong understanding of medical devices and equipment,including their design,development, and testing. Excellent analytical and problem-solving skills,with the ability to interpret complex data sets.

Conduct quality control checks on data accuracy and completeness.Provide training and support to staff on data management best practices.Ensure timely delivery of high-quality data products to stakeholders. Required Candidate profile Strong understanding of clinical trial operations and regulations. Experience with data management systems and software applications. Excellent analytical and problem-solving skills