Nukasani Group Inc
Only on w2 need submission details for Senior Manager, Clinical
Nukasani Group Inc, Marlborough, Massachusetts, United States, 01752
Dear Partner,
Good Morning ,Greetings from Nukasani group Inc !, We have below urgent long term contract project immediately available forSenior Manager, Clinical Supply Chain, Onsite
Marlborough, MA need submissions you please review the below role, if you are available, could you please send me updated word resume, and below candidate submission format details, immediately. If you are not available, any referrals would be greatly appreciated.
Interviews are in progress, urgent response is appreciated. Looking forward for your immediate response and working with you.
Candidate Submission Format - needed from youFull Legal NamePersonal Cell No ( Not google phone number)Email IdSkype IdInterview AvailabilityAvailability to start, if selectedCurrent LocationOpen to RelocateWork AuthorizationTotal Relevant ExperienceEducation./ Year of graduationUniversity Name, LocationLast 4 digits of SSNCountry of BirthContractor Type
: mm/dd
Home Zip Code
Assigned Job Details
Job Title : Senior Manager, Clinical Supply Chain
Location: Onsite
Marlborough, MARate : Best competitive rate
Position Overview
We are seeking an experienced Senior Manager, Clinical Supply Chain to oversee the planning, execution, and delivery of clinical supplies across multiple global programs. This individual will ensure Investigational Product (IP) availability and compliance while partnering cross-functionally with internal teams and external vendors to support end-to-end supply chain processes for early and late-phase clinical trials.
Key Responsibilities
Lead all clinical supply chain activities, including forecasting, packaging and labeling, distribution, inventory management, and returns/destruction for assigned studies.
Develop and manage supply chain plans and timelines in coordination with Clinical Operations and CMC teams.
Oversee IP inventory levels at manufacturing sites, depots, and clinical sites; ensure timely and accurate distribution of materials.
Design and review clinical label text to ensure regulatory compliance (U.S. and international
Ensure all supply chain activities meet applicable guidelines and regulations (GMP, GCP, ICH, FDA, international
Resolve logistical issues, including shipment delays, temperature excursions, and customs/import/export concerns in collaboration with Trade Compliance & Logistics teams.
Collaborate cross-functionally with Regulatory Affairs, Quality Assurance, Clinical Operations, and external CDMOs/CMOs.
Support clinical trial teams as the supply chain lead; provide updates on plans, timelines, and risks.
Manage clinical supply vendors, including contracts, purchase orders, invoices, and budgets.
Contribute to clinical supply chain budget forecasting and planning processes.
Demonstrate understanding of various clinical trial designs (e.g., randomized, blinded, open-label) and implications for supply planning.
Required Qualifications
Education:
Bachelors degree in Life Sciences, Business, or related discipline required
Masters degree preferred
Experience:
715 years of experience in the life sciences industry
Minimum 3 years specifically in clinical supply chain management
Background in project management, pharmaceutical development, or clinical trials coordination is highly desirable
Technical Skills:
Proficiency in Microsoft Excel, PowerPoint, and Microsoft Project
Strong understanding of clinical supply chain systems and global regulatory requirements
Certifications (Preferred):
APICS certification (CPIM, CLTD, or CSCP)
Soft Skills & Competencies
Excellent cross-functional communication and interpersonal skills
Strong organizational and problem-solving abilities
Ability to manage multiple projects and priorities in a fast-paced environment
Strategic mindset with strong attention to detail
Good Morning ,Greetings from Nukasani group Inc !, We have below urgent long term contract project immediately available forSenior Manager, Clinical Supply Chain, Onsite
Marlborough, MA need submissions you please review the below role, if you are available, could you please send me updated word resume, and below candidate submission format details, immediately. If you are not available, any referrals would be greatly appreciated.
Interviews are in progress, urgent response is appreciated. Looking forward for your immediate response and working with you.
Candidate Submission Format - needed from youFull Legal NamePersonal Cell No ( Not google phone number)Email IdSkype IdInterview AvailabilityAvailability to start, if selectedCurrent LocationOpen to RelocateWork AuthorizationTotal Relevant ExperienceEducation./ Year of graduationUniversity Name, LocationLast 4 digits of SSNCountry of BirthContractor Type
: mm/dd
Home Zip Code
Assigned Job Details
Job Title : Senior Manager, Clinical Supply Chain
Location: Onsite
Marlborough, MARate : Best competitive rate
Position Overview
We are seeking an experienced Senior Manager, Clinical Supply Chain to oversee the planning, execution, and delivery of clinical supplies across multiple global programs. This individual will ensure Investigational Product (IP) availability and compliance while partnering cross-functionally with internal teams and external vendors to support end-to-end supply chain processes for early and late-phase clinical trials.
Key Responsibilities
Lead all clinical supply chain activities, including forecasting, packaging and labeling, distribution, inventory management, and returns/destruction for assigned studies.
Develop and manage supply chain plans and timelines in coordination with Clinical Operations and CMC teams.
Oversee IP inventory levels at manufacturing sites, depots, and clinical sites; ensure timely and accurate distribution of materials.
Design and review clinical label text to ensure regulatory compliance (U.S. and international
Ensure all supply chain activities meet applicable guidelines and regulations (GMP, GCP, ICH, FDA, international
Resolve logistical issues, including shipment delays, temperature excursions, and customs/import/export concerns in collaboration with Trade Compliance & Logistics teams.
Collaborate cross-functionally with Regulatory Affairs, Quality Assurance, Clinical Operations, and external CDMOs/CMOs.
Support clinical trial teams as the supply chain lead; provide updates on plans, timelines, and risks.
Manage clinical supply vendors, including contracts, purchase orders, invoices, and budgets.
Contribute to clinical supply chain budget forecasting and planning processes.
Demonstrate understanding of various clinical trial designs (e.g., randomized, blinded, open-label) and implications for supply planning.
Required Qualifications
Education:
Bachelors degree in Life Sciences, Business, or related discipline required
Masters degree preferred
Experience:
715 years of experience in the life sciences industry
Minimum 3 years specifically in clinical supply chain management
Background in project management, pharmaceutical development, or clinical trials coordination is highly desirable
Technical Skills:
Proficiency in Microsoft Excel, PowerPoint, and Microsoft Project
Strong understanding of clinical supply chain systems and global regulatory requirements
Certifications (Preferred):
APICS certification (CPIM, CLTD, or CSCP)
Soft Skills & Competencies
Excellent cross-functional communication and interpersonal skills
Strong organizational and problem-solving abilities
Ability to manage multiple projects and priorities in a fast-paced environment
Strategic mindset with strong attention to detail