Research Senior Associate Jobs

Experience working on Clinical Trial Research and Clinical Research Trial Documentation

Previous experience within the Medical Device or Pharma industry

5+ years’ experience in Clinical Research

Comfortable working with a lot of documentation

Bachelor’s Degree – Any life sciences related degree

Advanced Project Management Skills is essential

4+ years experience working as a Senior Research Analyst/Research Manager/Project Manager

Experience in Animal Health/Pet Services is required for this role

Fantastic communication skills and a client-centric approach

We are actively seeking a Senior Research Manager to join our Animal Health team.

Day-to-day project lead of medium to high complexity projects for Animal Health

Bachelor’s degree required and/or significant equivalent work experience.

3-5 years of relevant professional experience, with experience working across public, private, and nonprofit sectors.

Excellent writing skills, with a proven track record of developing content that achieves desired results.

Demonstrated project administration skills, ability to multitask.

Excellent interpersonal, communication, presentation, and networking skills.

Experience working in – and able to travel periodically to -- emerging economies and sensitive to cultural and regional norms.

Education: Master’s Degree in a relevant field, including economics, public policy, environmental science, and engineering.

Strong working knowledge of economics for policy analysis

Excellent written and verbal communication skills

$60-$78,000 a year or potentially higher depending on experience

Commuter benefit plans (pre-tax metro and parking) 

Participate in engagement with decisionmakers and stakeholders

Proven experience with assays, such as PCR, ELISA, and /or mammalian cell culture.

Positive, professional self-starter with a passion for science, innovative technical and analytical skills required to perform at the highest level

Excellent clear and concise writing skills for technical reports and documents along with strong verbal communication skills

Experience in analytical method development and assay transfer

Be BOLD (Find a Way)

Care Deeply – for our patients, each other and our work

Hands-on experience with in vitro cell-based assays and ELISA assays is needed.

Screening assays for inhibition of cell proliferation and other general bioassays, including ELISA assays and PCR-based assays.

Preparation of necessary buffers and solutions will be needed if not purchased.

Keeping accurate records of experimental data and writing reports in a timely manner.

Present results to scientific team and management.

Experience in gene editing techniques, and/or small- to mid-scale suspension bioreactor processes, is highly preferred.

Excellent communication and presentation skills, capable of conveying complex biological data to non-experts

Plan and execute experiments, independently and collaboratively in cross-functional teams, to drive bioprocess development for immune cell therapies.

Master process development activities, including cell culture, cell engineering and gene editing; cell expansion; and cryopreservation.

Perform in-depth analyses of cell biology and functions using a variety of cell-based assays including flow cytometry.

A minimum of one (1) year experience in site oversight and management.

Expertise in oversight and managementvendors.

Company offers a great benefit package and competitive salary.

Assist the Study Lead carry out the responsibilities necessary to meet the constraints for the study.

Support clinical finance and the study's lead in evaluating, tracking, and directing study-specific budgets.

Three (3) or more years of experience in Clinical Research.

5+ years of experience in investment management or manager research

Proven experience and success in conducting open architecture manager research

Bachelors degree in business or related field, preferably with a major in finance or economics

Experience with Morningstar Direct, FactSet, eVestment, or similar tools

Experience covering offshore UCITS vehicles a plus

Must have excellent analytical, written, oral and interpersonal communication skills

3+ years of lab research experience on digital health technologies

Proven experience in scientific computing, data science and machine-learning especially Python

Excellent written and verbal communication and interpersonal skills

Experience conducting clinical studies as well as processing DHT and clinical study data.

*****COMPENSATION IS COMMSIERATE WITH EXPERIENCE*****

Responsible for acquiring and processing data collected using digital health technologies (DHT).

The ability to stay organized and manage multiple ongoing cultures/projects while keeping detailed notes.

Support scientists/senior scientists in implementing platform development studies and performing data analysis.

Participate in study design and platform development brainstorming sessions.

Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods.

Record all data and results with accuracy and responsibility.

Ensure that all safety guidelines are always followed strictly and maintain a clean and orderly environment.

Use good oral and written communication skills to relay scientific data

Maintain awareness of cutting-edge technical developments and scientific knowledge and apply these where possible to improve process efficiency

Hands-on experience in purification techniques including affinity, ion exchange, size exclusion, hydrophobic interaction chromatography using Akta Avant/Pure or BioRad NGC

Must be team-oriented, professional, hard-working, and interested in learning new skills.

Experience with other protein characterization technologies (DLS, SEC-MALS, LC/MS, IEX/HIC-HPLC) would be a strong plus

Experience in protein formulation, automated liquid handling systems (Hamilton, Bravo) would be a plus

Bachelor's degree with 3+ years of industry experience

Must have experience with mammalian cell culturing experience

Experience with cell transfection is a big plus

Some molecular biology knowledge is a plus

BS/MS degree in chemistry, pharmaceutical science, or related scientific discipline with 3+ years of relevant experience

Hands-on experience in method development and quantitative analysis of small molecule using LC-MS/MS instruments is highly desirable

Experience with in vitro ADME assays

Working knowledge of Phoenix WinNonLin software for PK analysis is a plus

Excellent communication and writing skills

Conduct LC-MS/MS method development to support drug/metabolites and biomarker analysis

Managing equipment induction activities including selection, procurement, qualification, and CSV

Reviewing and approving vendor-supplied qualification documentation

Maintaining current and accurate inventories of all equipment and software versions, including qualification status

Minimum of 2 years of experience in managing equipment commissioning, including CSV

Experience in assay method validations

Minimum of 5 years of experience in a quality role, preferably in a GLP environment

Highly motivated with excellent attention to detail. Good communication (oral and written) and collaboration skills.

Experience in cell culture and tissue preparation techniques.

Experience in troubleshooting and optimization of molecular biology assays including reagent formulation and workflow optimization.

Experience in product development including product release.

Advanced fluorescence imaging techniques. Experience in microscopy image analysis.

Additional Desirable Skills To Have

Oversee and manage clinical research projects and studies from initiation to completion

Manage and oversee data collection and analysis

Ensure compliance with regulatory requirements and guidelines

Prepares and maintains all IRB and regulatory paperwork to comply with institutional regulatory requirements

Bachelor's degree in a healthcare-related field or equivalent experience required

At least 3 years of experience in clinical research, including experience with clinical trials, required

Education, Experience And Skills Requirements

Any suitable combination of education, training, or experience is acceptable.

Evaluate new technologies and methodologies to support and advance analytical capabilities on the therapeutic products.

Handle and troubleshoot instrument issues such as on DNA sequencers and qPCR instruments.

Represent as subject matter expert on analytical molecular assays to support Chemistry, Manufacturing and Controls (CMC) team on new pharmaceutical products.

Supervise 2 Research Associate Contractors.

• Great career progression opportunities into management roles.

• Must be detail-oriented and efficient in time management;

This organisation will offer you the following and much more:

• Limitless training and development programs to benefit career advancement

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol

• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement