5955 Pharmaceutical Jobs - Page 50

Develop and implement project plans, resource allocation, and timelines for pharmaceutical projects.Collaborate with cross-functional teams to ensure successful project execution and delivery. Required Candidate profile Strong understanding of pharmaceutical project management principles and practices. Ability to work effectively in a fast-paced environment with multiple priorities and deadlines.

Develop high-quality medical content for various platforms, including reports and presentations.Conduct research and analyze data to create accurate and informative medical documents. Required Candidate profile Strong understanding of medical terminology and concepts. Excellent communication skills. Ability to work independently and as part of a team. Proficient in using computer software applications

Conduct thorough medical device safety assessments and evaluationsDevelop and implement effective safety protocols and proceduresCollaborate 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 fast-paced environment.

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Collaborate with cross-functional teams to ensure accurate and timely delivery of clinical data. Required Candidate profile Strong knowledge of Veeva EDC system and its applications in clinical trials. Experience in managing clinical data in a fast-paced environment. Excellent analytical and problem-solving

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations.Collaborate with cross-functional teams to ensure compliance with regulatory requirements Required Candidate profile Minimum 2 years of experience in regulatory writing, preferably in the pharmaceutical or healthcare industry. Strong understanding of regulatory requirements, including FDA, EMA, and ICH guidelines.

Collaborate with cross-functional teams to develop and implement clinical research studies.Provide medical expertise and guidance on study design, methodology, and statistical analysis. Required Candidate profile Strong understanding of clinical research principles, regulations, and guidelines. Excellent communication and interpersonal skills. Ability to work effectively in a team environment.

Identifying potential vendors in India and overseas, skilled negotiator, vendor evaluation, on-boarding procedures, setting technical specs for raw materials , equipment, civil items, handle and execute indents from the Plants, tendering process etc Required Candidate profile Products: Gums, Gum derivatives Hydrocolloids, Stabilisers, Gum blends for food, pet food, pharma, nutrition, personal care, Oil & Gas, Paper, Textiles, Explosives, Mining etc. BE/B.TEC/MBA MECH/CHEMI

Manage and maintain accurate clinical data records.Perform data reconciliation tasks to ensure accuracy and completeness.Collaborate with cross-functional teams to resolve data discrepancies Required Candidate profile Strong understanding of clinical data management principles. Proficient in data analysis and reporting tools. Excellent communication and problem-solving skills.

Manage and maintain accurate clinical data records, ensuring compliance with regulatory requirements.Perform data reconciliation tasks to ensure accuracy and consistency across systems.Collaborate with cross-functional teams 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 skills

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations.Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Minimum 2 years of experience in regulatory writing, preferably in the pharmaceutical or biotechnology industry. Strong knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines.

Manage and maintain accurate clinical data records, ensuring compliance with regulatory requirements.Perform data reconciliation tasks to ensure accuracy and consistency across systems.Collaborate with cross-functional teams Required Candidate profile Strong understanding of clinical data management principles and practices. Proficiency in data analysis and problem-solving skills with attention to detail.

Work Flexibility: Onsite Who we want: Hard-working winners. Confident, competitive and results-oriented professionals who create a track record of success. Dedicated achievers. People who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations. Effective communicators. People who can interpret information clearly and accurately to concisely communicate results and recommendations to stakeholders. Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices. What you will do: Relationship management ...

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Minimum 2 years of experience in regulatory writing, preferably in the pharmaceutical or biotechnology industry. Strong understanding of regulatory requirements,

Collaborate with cross-functional teams to develop and implement clinical research studies.Provide medical expertise and guidance on study design, methodology, and statistical analysis.Develop and maintain relationships Required Candidate profile Strong understanding of clinical research principles, regulations, and guidelines. Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders

Manage and oversee clinical 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 data management principles and practices. Experience with data management systems and technologies. Excellent communication and interpersonal skills.

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 fast-paced environment.

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 coding software and systems, such as Epic or Cerner. Familiarity with ICD-10-CM/PCS, CPT, and HCPCS Level II codes.

Manage and maintain accurate medical data records and databases. Ensure compliance with regulatory requirements and industry standards. Collaborate with cross-functional teams to achieve business objectives. Required Candidate profile Strong understanding of medical terminology and concepts. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment.

Conduct complex data analysis and interpretation to inform business decisions. Develop and implement innovative methods to measure and improve patient outcomes. Collaborate with cross-functional teams to design and execute studies. Required Candidate profile Strong understanding of health economics and outcomes research principles and practices. Proficiency in statistical analysis software such as SAS or R.

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 regulations and guidelines, including GCP and ICH. Experience with data management systems, such as Oracle or SQL.

Develop high-quality medical content for various platforms, including reports and presentations. Conduct thorough research on medical topics and stay updated with the latest developments. Required Candidate profile Collaborate with cross-functional teams to ensure accurate and consistent messaging. Create engaging and informative content that meets the needs of diverse audiences.

Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies to identify and resolve discrepancies. Required Candidate profile Strong understanding of clinical data management principles and practices. Proficiency in data analysis and interpretation software. Excellent problem-solving and communication skills.

Monitor medical enquiries and respond to queries from clients and stakeholders. Provide excellent customer service and ensure client satisfaction. Collaborate with internal teams to resolve medical enquiry issues. Required Candidate profile Strong communication and interpersonal skills are essential. Ability to work effectively in a fast-paced environment and prioritize tasks.

Develop and implement project plans, resource allocation, and timelines to ensure successful project execution. Collaborate with cross-functional teams to identify and mitigate risks. Required Candidate profile Excellent planning, organizational, and problem-solving skills, with the ability to prioritize tasks and manage multiple projects simultaneously.

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 case report forms.