Suraj Shaw
Sr. Manager, Proposals & Contracts- Clinical Research Services
- Role
- Sr Manager Proposals & Contracts at Parexel
- Location
- Hyderabad, TG, IN
- LinkedIn followers
- 500 followers
About Suraj Shaw
Over 19 years of working experience in serving Pharma, IT, CROs, SMO in role of Proposal Development (RFI, RFP, RFQ), Pre-Sales, Clinical Operations, Product Development Support and Business Development.• Over 16 years’ experience Business Analysis/Proposal Development (RFP/RFI/RFQs), Effort, resource and cost estimation for Clinical Operations, Clinical Data Management (CDM), Medidata Rave, Other EDC Systems, Biostatistics, Medical Writing, Pharmacovigilance, CDISC SDTM and Regulatory Submission Services in a reputed CRO environment• 2 years of experience in Business Development of Clinical Research Services, Clinical Research Central Lab Services and Clinical Research Training (ICH GCP, QA, Pharmacovigilance)• 1 year experience in Clinical Research Product Development (eDiary/ePRO), Risk Based Monitoring (RBM)• Core competencies include Proposal Development, Effort, Resource and Cost Estimation, Pricing & Budgeting, Business Analysis, Contract Management, Sourcing & Procurement, Vendor Management, Negotiation, Clinical Operations, Risk Based Monitoring (RBM), Product Development Support, Market Research and Competitive Analysis.
Experience
Sr Manager Proposals & Contracts
Jul 2025 — Present · Hyderabad, IN
Education
University of Calcutta
BSc, Biological Sciences
1999 — 2002
High Technologies Solutions
Certificate, SAS Base 9.1.3
2010 — 2010
North Orissa University
MSc, Biotechnology
2003 — 2005
Best Biotek Research Labs
Diploma, Clinical Research
2006 — 2007
Skills
- Standard Operating Procedure (Sop)
- Meddra
- Quality Assurance
- Vaccines
- Life Sciences
- Ich-Gcp
- Patient Recruitment
- Pharmaceutical Industry
- Sop
- Fda
- Pharmacovigilance
- Regulatory Submissions
- Clinical Study Design
- Crf Design
- Oncology
- Protocol
- Glp
- Clinical Data Management
- Oracle Clinical
- Drug Development
- Pharmaceutics
- Drug Discovery
- Gcp
- Biopharmaceuticals
- Data Management
- Edc
- Therapeutic Areas
- Ctms
- Clinical Development
- CRO Management
- Regulatory Affairs
- Lifesciences
- CRO
- Medical Writing
- Validation
- Medical Devices
- Clinical Research
- Clinical Monitoring
- Clinical Trial Management System (Ctms)
- Medical Affairs
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