Welcome to Scintillant Life Sciences Recruitment

Careers in Life Sciences

Top 10 Candidates

  • Biotechnology Business Development Professional
    21
    Feb
    Commercial Biotechnology Business Development Professional with over 15 years’ experience in Sales, Marketing, Business Development and R&D across several Life Science sectors.
  • Business Development & Portfolio Planning Professional
    21
    Feb
    An experienced Business Development, Licensing and Portfolio Planning Professional, currently Head of Department, with a strong mix of scientific, strategic planning and marketing expertise.
  • Applied Statistician
    21
    Feb
    An applied statistician with a strong scientific and technical background and extensive experience of manufacturing and R&D
  • Business Operations Manager
    16
    Nov
    Business Operations Manager with a mix of Engineering, Pharmaceutical and Medicinal Chemistry degrees and 12 years’ in-depth industry experience.
  • Professor Department of Molecular and Applied Biology
    07
    Oct
    PhD BEng(hons) BA CEng FIMechE FRSB, based in Kent, currently a professor of Molecular and Applied Biology
  • Clinical Contracts Manager
    03
    May
    Clinical Contracts Manager with Masters Degree in Intellectual Property
  • Microbiologist (Ref: 132215)
    12
    Feb
    Microbiologist, PhD Molecular Microbiology, with 6 years post-doc experience working within the Biotechnology industry. Primary focus, Virology.
  • Biomedical Scientist (Ref: 132218)
    12
    Feb
    Biomedical Scientist, State Registered, FIBMS with speciality in Haematology and Blood Transfusion. 5 years experience, post Fellowship, in routine Haematology laboratory of a major Regional Hospital ...
  • Molecular Biologist (Ref: 132221)
    11
    Feb
    Molecular Biologist, PhD in Cell and Molecular Biology with 3 years Post Doc experience in Academia and a further 3 years within the Pharmaceutical industry. Primary focus Genetics and Genomics.

Clinical and Regulatory Documentation Manager

Reference:
MI-Clin 2545212
Sector(s):
ADMET and DMPK, ADMET and DMPK, ADMET and DMPK, ADMET and DMPK, Analytical Chemistry, Analytical Chemistry, Analytical Chemistry, Biochemistry, Biochemistry, Biochemistry, Biochemistry, Biochemistry, Biochemistry, Bioengineering, Bioengineering, Bioengineering, Bioengineering, Bioinformatics, Bioinformatics, Bioinformatics, Bioinformatics, Bioinformatics, Bioinformatics, Biomedical, Biomedical Sciences, Biomedical Sciences, Biomedical Sciences, Biomedical Sciences, Biophysics, Biophysics, Biophysics, Biophysics, Biotechnology, Cell Biology, Cell Biology, Cell Biology, Cell Biology, Cell Biology, Cell Biology, Cell Signalling, Cell Signalling, Cell Signalling, Cell Signalling, Chemistry, Chemistry, Chemistry, Chemistry, Chemistry, Chemistry, Clinical Research, Clinical Research, Clinical Research, Clinical Research, Clinical Research, Diagnostics (in vitro), Diagnostics (in vitro), Diagnostics (in vitro), Diagnostics (in vitro), Diagnostics (in vitro), Diagnostics (in vitro), Drug Development, Drug Development, Drug Development, Drug Development, Drug Discovery, Drug Discovery, Drug Discovery, Drug Discovery, Genetics and Genomics, Genetics and Genomics, Genetics and Genomics, Genetics and Genomics, Genetics and Genomics, Genetics and Genomics, Genetics and Genomics, Immunology, Immunology, Immunology, Immunology, Immunology, Immunology, Immunology, In vitro Diagnostics, Manufacturing, Manufacturing, Manufacturing, Manufacturing, Manufacturing, Medical Communication, Medical Devices, Medical Education, Medical Writing, Metabolomics, Metabolomics, Metabolomics, Metabolomics, Metabolomics, Metabolomics, Microbiology, Microbiology, Microbiology, Microbiology, Microbiology, Microbiology, Microbiology, Molecular Biology, Molecular Biology, Molecular Biology, Molecular Biology, Molecular Biology, Molecular Biology, Nanotechnology, Nanotechnology, Nanotechnology, Nanotechnology, Nanotechnology, Nanotechnology, Neurosciences, Neurosciences, Neurosciences, Neurosciences, Neurosciences, Neurosciences, Pharmaceutical, Pharmacology, Pharmacology, Pharmacology, Pharmacology, Pharmacovigilance, Pharmacovigilance, Pharmacovigilance, Pre-Clinical, Pre-Clinical, Pre-Clinical, Proteomics, Proteomics, Proteomics, Proteomics, Proteomics, Quality Control and Assurance, Quality Control and Assurance, Quality Control and Assurance, Quality Control and Assurance, Quality Control and Assurance, Quality Control and Assurance, Regulatory, Regulatory, Regulatory, Regulatory, Research and Development, Research and Development, Research and Development, Research and Development, Research and Development, Research and Development, Stem Cells, Stem Cells, Stem Cells, Stem Cells, Structure Activity Relationship, Structure Activity Relationship, Structure Activity Relationship, Toxicology, Toxicology, Toxicology, Toxicology, Toxicology, Toxicology, Toxicology, Vaccines, Vaccines, Vaccines, Vaccines, Vaccines, Vaccines, Virology, Virology, Virology, Virology, Virology, Virology
Salary:
£37,200 Per Annum
Benefits:
+ bens
Town/City:
Cambridge
Contract Type:
Permanent

Description

We specialise in the recruitment of high quality candidates with expertise in Clinical and Regulatory Documentation. We have an excellent opportunity for an Administrator to join a global biotechnology / pharma company based in Cambridge.

Core Duties

The provision of administrative support for the company’s regulatory documentation management and for internal and external staff and company contracted clinical research organisations.

Key skills and knowledge

  • Understanding of global regulatory requirements and guidelines for conducting clinical trial and clinical research.
  • Knowledge of relevant GCP, external and internal regulatory requirements/guidelines
  • Project Management/planning experience
  • Ability to collaborate and build relationships to maximize organizational function and capabilities

Qualifications Required

  • Masters Degree OR
  • Bachelor’s Degree & 2 years directly related experience
  • Associates Degree & 5 years of directly related experience
  • High School diploma / GED & 8 years of directly related experience

Desirable Qualifications:

  • BS/BA/BSe in the sciences or RN
  • 2 years Clinical Documentation Management and industry experience (e.g. CTA/CRA/Study Manager) in order to have a thorough understanding of the processes associated with the conduct of clinical trials and document management operations.

Are you enthusiastic about this job? Send us your CV in word format today