Scientific Search specializes in Philadelphia Pharmaceutical Recruiting and staffing for a broad spectrum of technical and scientific positions within the Pharmaceutical, Biotechnology and Medical Device industries. We have a dedicated Philadelphia Pharmaceutical Recruiting team that focuses exclusively on this segment. Positions include technical, management and executive levels (including Directors and Vice Presidents) and many segments such as discovery research, clinical research, regulatory affairs, medical education, quality control, engineering, operations and marketing. Call or email us today and let us show you what our Philadelphia Pharmaceutical Recruiting team can do!
Some typical positions that we have placed are:
Continuing Medical Education (CME)
Medical Device Manufacturing
Medical Science Liaison (MSL)
Our internal database contains thousands of qualified pharmaceutical, biotech and medical device professionals that our Philadelphia Pharmaceutical Recruiting team has established relationships with. We are typically able to provide you with outstanding candidates within days of a request if not sooner. Here are some candidates our staff has identified as exceptional in what they do, and potentially high impact hires at their new organizations:
Featured Pharmaceutical Candidates
208,142 – Senior Director, Global Clinical Operations – Over 22 years oncology, and multiple other therapeutic areas and general clinical development experience. Led functional areas of multiple groups and over 140 internal employees. Oversight and Governance of multiple CROs and external relationships across Therapeutic areas and programs within Clinical Operations. Analyze and improve processes of clinical development and clinical operations. Lead a co-development partnership to deliver a clinical development program from phase I through phase III and submission preparation. Established the Clinical Operations strategy for all compound programs. Deliver on all operational and financial aspects of a ~370 M USD annual clinical development portfolio across all TAs. BS – Biology. For additional information on this exceptional candidate please contact Kim Laipple, firstname.lastname@example.org.
208, 037 – Director, Regulatory Affairs – *Will consider consulting or temporary opportunities* Over thirty years experience in consumer products-based companies. Actively supporting numerous US and international drug product applications, including initial phase of Rx to OTC switch IND. Design, review and approve labeling, advertising, promotional materials for marketed products, in accordance with FDA regulation, CHPA and FTC requirements. In addition, provided for the development, testing, and manufacture of OTC and prescription consumer products. Responsible for strategic market of new and existing over-the-counter monograph and application driven drug products. Author, advise on submissions/reports, insuring that all regulations of governing authorities are addressed. For additional information on this exceptional candidate please contact Kim Laipple, email@example.com.
196,059 – Scientific Director – *Will consider consulting or temporary opportunities* 18 years experience. Publication planning and development of strategy for oncology publications focused on solid and soft tissue tumors including leadership of publications committee. Provide professional expert advice based on current guidelines and apply best practices relating to development of medical publications. Writing and development of clinical publications based on company-sponsored preclinical and clinical studies for publication in peer-reviewed medical/scientific literature. Development of clinical study protocols, investigator brochures, clinical study reports and other clinical and regulatory documents. PhD – Pharmaceutical Sciences. For additional information on this exceptional candidate please contact Kim Laipple, firstname.lastname@example.org.
35,264 – Clinical Research Manager – *Will consider consulting or temporary opportunities* Overall Responsibilities include planning and conduct of a Global Pediatric Hematology Study. Additional Responsibilities include Feasibility as well as Country and Site Selection for 3 Hematology Studies. Direct responsibilities include management of CRO and multiple vendors. Manage project timelines, critical path milestones, clinical supply tracking, project budgets and vendors. Utilize project management analytical methods to assess progress and risks for assigned studies. Manage vendor quality control, delivery according to specifications, and overall performance assessment. Responsibilities for all operational aspects of study management including site management and monitoring, document management and management of clinical supplies globally. MS – Nursing. For additional information on this exceptional candidate please contact Kim Laipple, email@example.com.
202,198 – Controlled Substance Compliance Specialist – Extensive experience managing all DEA, OSHA, EPA and Safety items, maintaining all necessary paperwork to ensure compliance like DEA 222 forms, DEA registrations, DEA Procurement Quota, reporting, Import/Export permits, background checks, licenses, SOPs, OSHA forms. Designated site supervisor on company’s New York State Board of Pharmacy License for the R&D Laboratories/Office. Responsible for vault monitoring as well as overseeing other vault monitors and technicians, routinely handling controlled substances, hazardous waste, and medical waste. BS in Biology, Chemistry Minor; MBA in General Management. OSHA Certification. For additional information on this exceptional candidate please contact Kim Laipple, firstname.lastname@example.org.
190,535 – Biochemist / Manager – *Will consider consulting or temporary opportunities* 10+ years of Biopharmaceutical Industry experience and four years of Biotechnical industry experience. 10+ years of experience in the Analytical Development of PEG conjugated/ non-PEGylated protein therapeutics. Experienced in contributing to CMC sections of NDA and BLA submissions as well as authoring reports for regulatory submission. Participated in all phases of PEG-Protein drug development process for several potential drug candidates. These team activities resulted in the FDA approval of two anti-cancer protein drug products, and a third one in BLA submission. Excellent understanding of the drug development process, laboratory quality systems and applicable regulatory requirements. PhD – Biochemistry. For additional information on this exceptional candidate please contact Kim Laipple, email@example.com.