Delivering top talent and senior leaders in the life sciences industry.
Whether you need to find a regulatory affairs director, medical device engineer, clinical research manager or life science professional, Scientific Search is here to help find and hire the best candidates.
Our internal database contains thousands of qualified pharmaceutical, biotech, clinical research, cell and gene therapy, and medical device professionals that we have established relationships with. We are typically able to provide you with outstanding candidates within days of a request if not sooner.
We’ve all been there — burning through time and resources trying to fill a critical hiring need while managing a host of other obligations. Scientific Search’s sole focus is to place thoroughly vetted, qualified individuals with verifiable excellent backgrounds and solid interest in the opportunity you offer at your fingertips. Within 5 business days of starting a new search for any of our Pharmaceutical and Biotechnology clients, we’ve already spoken with over 70% of our client’s targeted high performers and presented the 5 best transformational leaders to them.
Pharma Positions We Typically Fill
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Biostatistics
Brand Management
Business Development
Chemists/Scientists
Clinical Operations
Clinical Research
CMC
Commercial Manufacturing
Compliance
DMPK
Documentation Control
Drug Safety
EH&S
Engineering
Facilities Management
Formulations
Health Economics
Information Technology
Laboratory Professionals
LIMS
Market Access
Marketing
Medical Affairs
Medical Directors
Medical Science Liason
Operations
Packaging
Pharmacovigilance
Physicians
Product Development
Project Management
Quality Assurance
R&D
Regulatory Affairs
Sales Management
Statisticians
Supply Chain
Technology Transfer
Toxicology
Validation
Positions include technical, management and executive levels (including Vice Presidents and Directors) and many segments from pre-clinical research, clinical studies, commercialization, and manufacturing support.
Scientific Search specializes in Pharmaceutical Recruiting and Staffing for a broad spectrum of technical, management, and executive positions within the Life Sciences industry. Business segments include Pharmaceutical, Biotech, Clinical Research, Real World Evidence (RWE), Cell & Gene Therapy and Medical Devices.
Biostatistics
Brand Management
Business Development
Chemists/Scientists
Clinical Operations
Clinical Research
CMC
Commercial Manufacturing
Compliance
DMPK
Documentation Control
Drug Safety
EH&S
Engineering
Facilities Management
Formulations
Health Economics
Information Technology
Laboratory Professionals
LIMS
Market Access
Marketing
Medical Affairs
Medical Directors
Medical Science Liason
Operations
Packaging
Pharmacovigilance
Physicians
Product Development
Project Management
Quality Assurance
R&D
Regulatory Affairs
Sales Management
Statisticians
Supply Chain
Technology Transfer
Toxicology
Validation
Positions include technical, management and executive levels (including Vice Presidents and Directors) and many segments from product design and development to capital projects and manufacturing support.
Scientific Search specializes in Pharmaceutical Recruiting and Staffing for a broad spectrum of technical, management, and executive positions within the Life Sciences industry. Business segments include Pharmaceutical, Biotech, Clinical Research, Cell & Gene Therapy and Medical Devices.
Our Featured Candidates
Chief Medical Officer
(CN#554443)
20 years' experience
- Has led two oncology drugs to approval
- Building a preclinical research strategy
- Setting up clinical budget with human resource allocation
- Responsible for leading the clinical effort and responsibility for overseeing pharmacovigilance /safety
- Medical Doctor; MS - Clinical and Pharmacological Research; Clinical Oncology Specialist
Director, Diagnostic Assay
(CN#552819)
15+ years' experience
*Will consider consulting or temporary opportunities*
- Director Level Leadership; Diagnostics, R&D
- R&D leader in developing 4 FDA-cleared Solana products: Trichomonas, HSV 1+2-VZV, GBS, and Bordetella Complete.
- R&D leader in developing 4 FDA-cleared AmpliVue products: C diff, GBS, Bordetella, and Trichomonas assays.
- Principal contributor in developing lateral flow detection of the helicase-dependent amplification product using DNA test strip.
- BS & MS Biology, Ph.D. Biochemistry
Associate Director, Biostatistics
(CN#152083)
20+ years' experience
- Serves as statistical lead on oncology drug
- Experience designing phase 1 through 3 studies with Clinical Development
- Wrote SAS programs to verify statistical analyses, including topline results; prepared topline reports
- Develop statistical submission package to regulatory agency including FDA and EMA; write ISS, ISE SAPs; assist in RMP development
- M.S. Applied Mathematics and Statistics, Stony Brook University; B.S. Microbiology
Senior Manager, Regulatory Affairs CMC
(CN#521398)
20 years' experience
*Will consider consulting or temporary opportunities*
- Technical Writing, Deviation investigations, root cause analysis, CAPA and contributions to CMC regulatory submissions.
- Authored CMC sections for IND, BLA, NDA, eCTD (Lorenz Docubridge) etc.
- Lead process development programs for non-virally modified cellular therapeutics encapsulated in alginate spheres.
- Lead CMC/Regulatory Affairs activities, managed stability programs for cell therapy drug substances and drug products.
- Ph.D.- Biochemistry/Immunology/Glycobiology
Global Regulatory Lead
(CN#345128)
20+ years' experience
- Primary author of all regulatory submissions including meeting packages, briefing books, amendments, supplements
- Serves as lead for all IND, NDA, and MAA submissions both strategically and operationally
- Served as Point person for regulatory agency interactions
- Experience in various therapeutic areas
- Master of Science; Molecular and Developmental Biology
Manager, Quality Systems Programmer
(CN#557054)
32 years' experience
*Will consider consulting and temporary opportunities*
- Experienced in FDA remediation from warning letters, 483 observations and internal/external audits.
- Proficient in requirements of the USP, JP, EP, BP and AOAC.
- Expert in Good Manufacturing Practices, Good Documentation Practices and all areas of Data Integrity (ALCOA-PLUS). Excelled in FDA audits for both cGMP inspections and pre-approval inspections, never receiving any “observations” by the FDA
- Experienced in all Quality Control Chemistry Laboratory, and R&D Laboratory instruments including HPLC, UPLC, GC, FTIR, KF, UV, automation titrators, MasterSizer, as well as most forms of bench chemistry.
- BS - Biology
I want to say thanks for your help on this, you have been very responsive and have been sending quality candidates. I have worked with a lot of agencies since I’ve been here and you all have done a very good job with quality candidates and speed of response, which are both super important, so thanks again!
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