Manager -Biospecimen
Bristol-Myers Squibb
Manager -Biospecimen
Job Description
Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision. Clinical Team member responsible for providing shipping/sample movement and management including requests, query and inventory reports, follow up active issues with vendors, prepare sample management related reports, review/prepare tracking activities (such as vendor manifests/inventories, tissue/blood match pairing, depleted/non-viable samples, loading documents to Shared Drive folders, etc.). Independently reviews clinical study protocol providing comparison of vendor statement of work and biospecimen relevant sections and feedback with support as needed. Performs routine vendor management responsibilities. Able to request and/or access necessary vendor/system inventory files to perform specimen tracking. Able, under direction, to create biospecimen tracker using various tracking tools (MS Excel, Spotfire, Tableau or internal systems (if applicable)). Exercises judgment within policy and procedure boundaries. Troubleshoots routine problems and understands when appropriate to ask for guidance. Minimum of 3-4 years academic, biotech, healthcare or pharmaceutical industry experience or equivalent. Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues. Demonstrated clinical trial experience, healthcare/medical/laboratory or equivalent. Vendor experience preferred (e.g., Central Labs, Bioanalytical, Biomarker, CROs, Biospecimen Storage Vendors, etc.). Biospecimen management experience preferred but not mandatory. Ability to effectively communicate, create and deliver presentation/information/data to knowledgeable audiences, with limited supervision. Ability to adopt a biopharma enterprise-wide and entrepreneurial mindset, to act with a sense of urgency, accountability and integrity, and to have fun along the way. Travel requirement is minimal, 0%- 5% of time, when organization requests
Key Responsibilities
- Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision
- Provide shipping/sample movement and management including requests, query and inventory reports
- Follow up active issues with vendors
- Prepare sample management related reports
- Review/prepare tracking activities such as vendor manifests/inventories, tissue/blood match pairing, depleted/non-viable samples, loading documents to Shared Drive folders
- Independently review clinical study protocol and provide comparison of vendor statement of work and biospecimen relevant sections with feedback
- Perform routine vendor management responsibilities
- Request and/or access necessary vendor/system inventory files to perform specimen tracking
- Create biospecimen tracker using various tracking tools (MS Excel, Spotfire, Tableau or internal systems)
- Exercise judgment within policy and procedure boundaries
- Troubleshoot routine problems and understand when to ask for guidance
Required Qualifications
- Minimum of 3-4 years academic, biotech, healthcare or pharmaceutical industry experience or equivalent
- Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues
- Demonstrated clinical trial experience, healthcare/medical/laboratory or equivalent
Preferred Qualifications
- Vendor experience (e.g., Central Labs, Bioanalytical, Biomarker, CROs, Biospecimen Storage Vendors, etc.)
- Biospecimen management experience
Skills Required
- Ability to effectively communicate, create and deliver presentation/information/data to knowledgeable audiences with limited supervision
- Ability to adopt a biopharma enterprise-wide and entrepreneurial mindset
- Ability to act with a sense of urgency, accountability and integrity
- Ability to have fun along the way
Additional Requirements
- Travel requirement is minimal, 0%-5% of time, when organization requests
Locations
- Hyderabad TS, India
Salary
Estimated Salary Rangemedium confidence
1,200,000 - 2,400,000 INR / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to effectively communicate, create and deliver presentation/information/data to knowledgeable audiences with limited supervisionintermediate
- Ability to adopt a biopharma enterprise-wide and entrepreneurial mindsetintermediate
- Ability to act with a sense of urgency, accountability and integrityintermediate
- Ability to have fun along the wayintermediate
Required Qualifications
- Minimum of 3-4 years academic, biotech, healthcare or pharmaceutical industry experience or equivalent (experience)
- Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues (experience)
- Demonstrated clinical trial experience, healthcare/medical/laboratory or equivalent (experience)
Preferred Qualifications
- Vendor experience (e.g., Central Labs, Bioanalytical, Biomarker, CROs, Biospecimen Storage Vendors, etc.) (experience)
- Biospecimen management experience (experience)
Responsibilities
- Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision
- Provide shipping/sample movement and management including requests, query and inventory reports
- Follow up active issues with vendors
- Prepare sample management related reports
- Review/prepare tracking activities such as vendor manifests/inventories, tissue/blood match pairing, depleted/non-viable samples, loading documents to Shared Drive folders
- Independently review clinical study protocol and provide comparison of vendor statement of work and biospecimen relevant sections with feedback
- Perform routine vendor management responsibilities
- Request and/or access necessary vendor/system inventory files to perform specimen tracking
- Create biospecimen tracker using various tracking tools (MS Excel, Spotfire, Tableau or internal systems)
- Exercise judgment within policy and procedure boundaries
- Troubleshoot routine problems and understand when to ask for guidance
Travel Requirements
5%
Tags & Categories
Answer 10 quick questions to check your fit for Manager -Biospecimen @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs
Manager -Biospecimen
Bristol-Myers Squibb
Manager -Biospecimen
Job Description
Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision. Clinical Team member responsible for providing shipping/sample movement and management including requests, query and inventory reports, follow up active issues with vendors, prepare sample management related reports, review/prepare tracking activities (such as vendor manifests/inventories, tissue/blood match pairing, depleted/non-viable samples, loading documents to Shared Drive folders, etc.). Independently reviews clinical study protocol providing comparison of vendor statement of work and biospecimen relevant sections and feedback with support as needed. Performs routine vendor management responsibilities. Able to request and/or access necessary vendor/system inventory files to perform specimen tracking. Able, under direction, to create biospecimen tracker using various tracking tools (MS Excel, Spotfire, Tableau or internal systems (if applicable)). Exercises judgment within policy and procedure boundaries. Troubleshoots routine problems and understands when appropriate to ask for guidance. Minimum of 3-4 years academic, biotech, healthcare or pharmaceutical industry experience or equivalent. Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues. Demonstrated clinical trial experience, healthcare/medical/laboratory or equivalent. Vendor experience preferred (e.g., Central Labs, Bioanalytical, Biomarker, CROs, Biospecimen Storage Vendors, etc.). Biospecimen management experience preferred but not mandatory. Ability to effectively communicate, create and deliver presentation/information/data to knowledgeable audiences, with limited supervision. Ability to adopt a biopharma enterprise-wide and entrepreneurial mindset, to act with a sense of urgency, accountability and integrity, and to have fun along the way. Travel requirement is minimal, 0%- 5% of time, when organization requests
Key Responsibilities
- Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision
- Provide shipping/sample movement and management including requests, query and inventory reports
- Follow up active issues with vendors
- Prepare sample management related reports
- Review/prepare tracking activities such as vendor manifests/inventories, tissue/blood match pairing, depleted/non-viable samples, loading documents to Shared Drive folders
- Independently review clinical study protocol and provide comparison of vendor statement of work and biospecimen relevant sections with feedback
- Perform routine vendor management responsibilities
- Request and/or access necessary vendor/system inventory files to perform specimen tracking
- Create biospecimen tracker using various tracking tools (MS Excel, Spotfire, Tableau or internal systems)
- Exercise judgment within policy and procedure boundaries
- Troubleshoot routine problems and understand when to ask for guidance
Required Qualifications
- Minimum of 3-4 years academic, biotech, healthcare or pharmaceutical industry experience or equivalent
- Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues
- Demonstrated clinical trial experience, healthcare/medical/laboratory or equivalent
Preferred Qualifications
- Vendor experience (e.g., Central Labs, Bioanalytical, Biomarker, CROs, Biospecimen Storage Vendors, etc.)
- Biospecimen management experience
Skills Required
- Ability to effectively communicate, create and deliver presentation/information/data to knowledgeable audiences with limited supervision
- Ability to adopt a biopharma enterprise-wide and entrepreneurial mindset
- Ability to act with a sense of urgency, accountability and integrity
- Ability to have fun along the way
Additional Requirements
- Travel requirement is minimal, 0%-5% of time, when organization requests
Locations
- Hyderabad TS, India
Salary
Estimated Salary Rangemedium confidence
1,200,000 - 2,400,000 INR / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Ability to effectively communicate, create and deliver presentation/information/data to knowledgeable audiences with limited supervisionintermediate
- Ability to adopt a biopharma enterprise-wide and entrepreneurial mindsetintermediate
- Ability to act with a sense of urgency, accountability and integrityintermediate
- Ability to have fun along the wayintermediate
Required Qualifications
- Minimum of 3-4 years academic, biotech, healthcare or pharmaceutical industry experience or equivalent (experience)
- Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues (experience)
- Demonstrated clinical trial experience, healthcare/medical/laboratory or equivalent (experience)
Preferred Qualifications
- Vendor experience (e.g., Central Labs, Bioanalytical, Biomarker, CROs, Biospecimen Storage Vendors, etc.) (experience)
- Biospecimen management experience (experience)
Responsibilities
- Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision
- Provide shipping/sample movement and management including requests, query and inventory reports
- Follow up active issues with vendors
- Prepare sample management related reports
- Review/prepare tracking activities such as vendor manifests/inventories, tissue/blood match pairing, depleted/non-viable samples, loading documents to Shared Drive folders
- Independently review clinical study protocol and provide comparison of vendor statement of work and biospecimen relevant sections with feedback
- Perform routine vendor management responsibilities
- Request and/or access necessary vendor/system inventory files to perform specimen tracking
- Create biospecimen tracker using various tracking tools (MS Excel, Spotfire, Tableau or internal systems)
- Exercise judgment within policy and procedure boundaries
- Troubleshoot routine problems and understand when to ask for guidance
Travel Requirements
5%
Tags & Categories
Answer 10 quick questions to check your fit for Manager -Biospecimen @ Bristol-Myers Squibb.
10 Questions
~2 Minutes
Instant Score
Related Books and Jobs