Bevov

Bevov Bevov is an AI-enabled recruiting solution that connects BioPharma companies to qualified, interview

08/16/2021

Job scope:
Bevov is expanding and looking for a strong Pharmaceutical/ Healthcare Recruiter to join our Talent Community. The Recruiter(s) is responsible for Service Excellence throughout the recruitment cycle and acts as a brand ambassador and partners with the hiring managers in a consultative capacity.

Job description
Responsible for the full life cycle recruitment process of all levels.
Complete a detailed job scope conversation with the hiring leader to determine position specifications.
Timely review of applicants who have applied via the Platform.
Coordinate with the Hiring Managers for the interview process.
Ensure all candidates are provided with timely updates concerning the status of their applications and interviews.
Throughout the process, keep a strong pulse on the top candidates' interest levels and/or concerns.
Proven expertise in volume hiring for generic skills & recruitment for niche & strategic positions.

Qualifications:
Bachelor’s/Master’s degree in Pharma, Sciences, Business, management, human resources, or related field preferred.
Minimum 3+ years of in-house, RPO, or agency recruiting experience.
Pharmaceutical/Biotech industry experience is highly preferred.
Demonstrated ability to handle difficult and demanding customers.
Ability to possess a high sense of urgency while working in a constantly changing environment.
Experience being a part of a new launch/expansion is strongly preferred
Adhere to documentation and processes for compliance.

08/16/2021

Job Overview
Bevov hires people to connect BioPharma companies of all sizes with the most qualified industry professionals. We built the first AI matching technology specifically for the BioPharma industry to deliver qualified interview-ready candidates. Your talents, ideas, and passion are essential to our mission. And to continue with our mission, we are looking for a Sourcer who can deliver interview-ready candidates in the BioPharma industry.

Job Responsibilities
Writing and implementing effective research strategies to source diverse candidates on each requisition.
Using all possible means to engage those candidates quickly and ensuring up-to-date CVs are received from potential candidates.
Provide strategic input on best sourcing channels.
Assist with building short-and long-term pipelines according to hiring priorities
Uncover top talent using a wide variety of tools such as LinkedIn Recruiter, Boolean searches, targeted name generation, social networking, professional associations, and mining databases or job boards.

Job Requirements
Bachelor's Degree or equivalent experience
Minimum 2+ years of sourcing experience, the biopharma industry is a huge plus
Excellent interpersonal communication and customer service skills, resourceful
Highly collaborative and strong team player in a fast-paced and changing environment
Proactive, ability to multitask, and execute tasks with limited supervision
Excellent organizational skills, ability to adapt quickly and be flexible

Benefits
Enjoy working remotely from the comfort of your home.
Be part of the fun and collaborative team.
Bevov is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, s*xual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.

08/16/2021

Who We Are:
Bevov is the world’s first AI-enabled candidate sourcing platform catered specifically to the BioPharma industry. Our technology delivers higher-quality candidates faster, and more cost-efficiently than any other solution in the BioPharma industry. Our HQ is located in Silicon Valley and development team in Hyderabad

Roles and Responsibilities:
Good understanding with hands-on experience on core PHP and ensuring all code that goes to production is of top quality.
Ensure existing applications are scaled to meet expected demand.
Identify and fix gaps in system reliability, such as production monitoring.
Continuously improve the software infrastructure, such as the deployment process
Investigate and fix production issues and ability to do Unit testing
Ability to work independently, manage tasks, and report/present efforts to the management team.
Ability to take lead and work in a fast-paced working environment.

Mandatory Skills:
Excellent knowledge of the core PHP 5/7 or web server exploits along with their solutions and experience building or maintaining custom MVC frameworks.
A detailed understanding of database design, administration, and performance tuning, with a preference for those with MySQL experience.
Excellent hands-on experience of working with modern standards-based HTML, CSS (SASS/LESS), Javascript, JQuery & AJAX
Proficiency when it comes to code versioning tools.

Good to have skills :
Experience in Python and Elasticsearch
Experience in Laravel & PHP frameworks such as CI/CakePHP/Yii.
Experience in Angular/React/Vue js
Partner with the required teams and get seamless outputs.
Should be curious to learn more and collaborate whenever needed.
Strong communication skills.

05/12/2021

Our client is seeking highly motivated and creative scientists to help us develop life-changing diagnostics and therapeutics for Alzheimer’s Disease. The Scientist uses deep knowledge of scientific principles and concepts along with technical and analytical proficiency, thoughtful scientific creativity, dogged determination, collaboration with others, and an enthusiastic spirit to tackle a formidable devastating disease. You have experience in neurodegeneration, diagnostic or drug development, and/or developing and engineering new approaches in this area. You have a strong background in data analysis and attention to detail. You are meticulous while being boldly creative. You always remain focused on the human objective: early diagnosis and treatment for patients and a sense of urgency as part of a dynamic, committed team.

You may lead a project or initiative involving other contributors. You may supervise the activities of more junior personnel and be responsible for driving the development of those employees. You will contribute toward peer-reviewed publications, the invention of IP, internal reports, and/or regulatory filings. You are eager to learn new techniques and approaches
Responsibilities
Contribute to preclinical in-house development of therapeutic candidates and pre-IND development activities
Lead significant components of drug development or other related projects
Contribute to diagnostic development, optimization, and testing
Contribute toward regulatory studies and clinical trials of diagnostic test
Independently design, execute and interpret multiple studies. Design experiments to be carried out by self and others.
Motivate and support others, setting clear goals and expectations
Author and review technical reports, manufacturing documents, regulatory submissions, and publications
Present at department, project team, and senior management meetings. May present externally at scientific conferences
Qualifications
Deep knowledge of peptide/protein chemistry, structures, and interactions. Strong in analytical, organic, and physical chemistry techniques.
Good understanding of analytical and conformational protein characterization (including HPLC, MS, CD, functional assays)
Experience with peptide therapeutics and their delivery
Experience with ELISAs, cell culture, handling human samples, chemical modifications, protein structural studies, planning animal experiments, analytical techniques, statistical analysis of results, pharmaceutical formulation, assay optimization
Ph.D. in chemistry, biochemistry, chemical engineering, bioengineering, or related field with 3+ years of industry or postdoctoral experience

Benefits
The client offers a competitive compensation package as well as a benefits program designed to support the well-being of our employees and their families. Benefits include medical, vision, and dental coverage, and group life insurance.

The client is an equal opportunity employer with the desire for diversity of all types. All qualified applications will receive consideration for employment without regard to race, age, gender identity, s*xual orientation, color, religion, s*x, marital status, national origin, disability, or any other status protected by federal, state, or local law.

05/12/2021

Our client is a private aquaculture innovation and research company is seeking a Research Associate to assist in the daily operations of its Genotyping lab in San Diego, CA and will begin with the successful candidate reporting to the Genotyping Lab Manager.

Responsibilities
Assist with laboratory experiments on research projects
Sample processing and genotyping
Sample processing and genotypingPerform Next Generation Sequencing (NGS) library (e.g. amplicon-seq, RNASeq, GBS) preparation/QC for Ion or Illumina Platforms, however previous experience with Illumina-based sequencing platforms will be applicable. Specific experience with Ion NGS platforms (S5) preferred
Develop and deploy appropriate automation to aid processing and improve throughput on the genotyping platforms.
Assist in developing SNP panels and associated assays for various species [varied platforms from PCR to Next Generation Sequencing (NGS)].
Perform sample processing and DNA/RNA extraction using automated nucleic acid platforms (e.g. Kingfisher), and assist in optimization efforts to improve throughput and efficiencies.
Troubleshooting to improve processes and data consistency and quality.
Assist with design and implementation of client and internal R/D research projects.
Coordinate with Research Technicians on training and troubleshooting processes; and participate in laboratory upkeep including equipment maintenance, vendor sourcing and restocking supplies, and maintaining inventories.
Qualifications
Bachelor’s degree in Biology, Biological Sciences, Life Science, and/or a related field is required.
Knowledge of general molecular biology and demonstrated experience with assay development and associated instrumentation in DNA/RNA extraction, nucleic acid quantification, PCR amplification, qPCR, liquid handling, NGS library preparation [experience with Ion sequencing technologies preferred].
Good computer skills including proficiency with Microsoft Office are required.
Must be able to communicate effectively in both group and one on one settings.
Must be organized, detail-oriented and meticulous in following set protocols and record keeping.
Ability to multitask and meet deadlines in a fast-paced, production environment.
Excellent English (both verbal and written) is required
Benefits
Health and dental benefits
Life insurance/AD&D/LTD
401k we match 50% up to a max of 6%
20 vacations days
10 sick days

05/12/2021

Our client has an exciting Life Science opportunity to join our rapidly growing team developing novel protein Kinase activity assays and offering Custom Testing Services that enable our clients. Their innovative and patented fluorescence-based sensor technology is exclusively licensed from MIT.

Responsibilities
Highly motivated and self-driven - Thrive in a fast-paced and interdependent working environment.
Excellent technique including small volume dispensing and strong attention to detail.
Ability to master new techniques, find solutions and effectively multitask to achieve goals efficiently.
Strong computer skills including Microsoft Office/Access and scientific/data analysis software.
Demonstrated organizational, documentation, and oral communication skills with the ability to work independently and as a team
Practical knowledge of fluorescence-based activity assays to assess enzyme kinetics and drug potency.
Qualifications
Bachelor's or advanced degree in biology, chemistry, biochemistry, etc.
4-10 years hands-on lab experience developing or using quantitative microtiter plate-based assays, including routine assessment of drug potency.
Familiarity with modern automation instrumentation and software for drug discovery assays.
Industry experience with demonstrated productivity analyzing enzyme inhibitors.
Benefits
Our client is an Equal Opportunity Employer (EOE) and strongly supports diversity in the workplace.

05/12/2021

The Senior Biostatistician will be responsible for designing statistical analysis plans for clinical studies; performing statistical analyses independently; creating reports intended for internal distribution and for regulatory submission; creating internal presentations and white papers. His/her work will follow and will adhere to applicable regulations for pre-and post market clinical trials. S/he ensures statistical analyses are conducted with the highest level of scientific integrity while meeting timelines and budgets. Reporting to the Biostatistics Manager.

Responsibilities
Interact with Biostatistics, Data Management, Regulatory, and Clinical staff to define and clarify project requirements.
Design and execute statistical plans for all phases of clinical studies of moderate complexity under limited supervision.
Review clinical study protocols and Case Report Forms (CRFs) for proposed studies with respect to statistical methodology.
Generate randomization schemes; unblind treatment assignments and handle unblinded information appropriately.
Support the review and assessment of protocol deviations to the extent that they affect statistical analyses.
Produce statistical reports that may be incorporated into internal clinical reports or regulatory submissions.
Contribute to peer-reviewed articles independently, in coordination with the lead author/physician.
Review articles on topics relevant to specified products and provide reports concerning issues relating to statistical methodology.
Assist with preparation of documentation for IRB/Ethics Committee submissions (e.g., statistical power analysis).
Assist in the preparation and documentation of results to support trial reports and publications.
Resolve complex statistical issues from business units and external customers.
Provide statistical reports for data quality/performance metrics.
Assist Clinical Research with literature reviews and other activities.
May assist in preparing information and materials for presentation at professional meetings.
Stay current with statistical methodology in clinical trial design and analysis
Qualifications
A Master’s degree or Ph.D. in Statistics is preferred
At least 3 years of experience performing statistical analyses in a regulated environment, preferably medically related including FDA, GCP, or other relevant areas.
Demonstrated technical experience in preparing statistical deliverables on time.
Thorough understanding of descriptive statistics, hypothesis testing, non-parametric, and multivariate statistical tests.
Ability to assist in selecting and applying methods and analyses in the field of application
Understand the processes involved in strategic planning.
Experience with survival analysis, longitudinal data analysis, and other current, innovative statistical methodologies.
Excellent verbal and written communication skills.
Knowledge of Microsoft packages; PowerPoint, Excel, Word.
Proficient in SAS. Familiarity with other statistical packages for handling smaller datasets and power analyses.

05/12/2021

Job Description
Our Client is looking for an experienced protein biochemist to join the company’s drug discovery efforts. S/he is expected to play a central role in efforts to identify and progress lead LYTAC programs through their work in bioconjugation. A successful candidate has a solid base in amino acid chemistry and working with recombinant proteins and antibodies. This includes protein purification and the synthesis and analysis of antibody-drug conjugates (ADCs). A broad scientific background with a recent emphasis on ADCs may be ideal as occasional forays outside the central role of bioconjugation are likely.

Responsibilities
Conduct antibody conjugation reactions at small and large scale using commonly employed lysine and cysteine chemistry.
Optimize synthetic procedures and purification protocols for ADCs to maximize both the efficiency of conjugation and product stability.
Analytical characterization of ADCs and naked Mabs by LC-MS, SEC, IEC, and SDS-PAGE.
Assess binding characteristics ADCs in vitro.Occasional assessment of ADC bioactivity in cell-based assays.
Maintain an accurate database of ADCs.
Analyze, document, and report data.
Present unbiased results in regular group meetings
Qualifications
BS/MS in biochemistry or related field with a minimum of 2 years experience in the chemical conjugation of proteins and 7+ years total lab experience.
Experience with intact mass analysis of proteins and/or ADCs by LC-MS.Use of AKTA systems for protein purification via SEC, IEC, and affinity chromatography.
Experience with analytical SEC and reverse phase chromatography (HPLC).
Sound understanding of biological buffers and the effect of pH on amino acid chemical reactivity.
Sound understanding of protein stability and the ability to determine when a reagent (protein or ADC) is compromised.
Experience with endotoxin testing and prevention of endotoxin contamination of equipment and reagents.
Basic tissue culture skills and understanding of data generated in cell-based functional assays.
Experience with electronic notebooks.
Experience with Biacore or Octet desired but not required
Benefits
Our client is an equal opportunity employer and value diversity at their company. They do not discriminate on the basis of race, religion, color, national origin, gender, s*xual orientation, age, marital status, veteran status, or disability status

05/12/2021

Our client is looking for a highly motivated and enthusiastic scientist to join the company’s research drug discovery efforts and lead our biologics purification platform and research capabilities. S/he is expected to help champion purification & characterization efforts of lead LYTAC programs. A successful candidate has a thorough knowledge of purification theory and a demonstrated history advancing research molecules into pre-clinical development.

Responsibilities
Purification of lead/reagent antibodies from mammalian tissue culture (hybridoma, 293, CHO)
Purification of recombinant proteins for research pipeline/assay development including soluble ligands and extracellular domain fusions
Expert in FPLC-AKTA / Unicorn software station and process flows
Expert in Affinity purification (protein A, His-tag, FLAG-tag)
Expert in protein chromatography (Gel filtration, IEX, HIC, multi-modal resins), and applicability from mg to gram scale
Purification of LYTAC conjugated biomolecules (non-specific and site-specific conjugation chemistries)
Early formulation development for lead LYTAC programs
Work independently on the design, ex*****on, and interpretation of experimental results.
Coordinate activities with functional groups and project teams
Analyze, document, and report data concisely and rigorously.
Qualifications
Ph.D. in biophysics, biochemistry, or related field, with relevant post-doctoral research or MS with 10 years of industry experience
Demonstrated history of accomplishments via high impact publications and/or advancing molecules from research into pre-clinical/IND activities
Candidates with relevant industry experience will be given preferential consideration for this position
Experience in a wide variety of analytical and physicochemical techniques including chromatography (High- Performance Liquid Chromatography: HPLC, Capillary Electrophoresis: CE), Surface Plasmon Resonance (SPR – Biacore and/or Octet), Light scattering (DLS/MALS), LC/MS characterization
Working knowledge of bi-specific antibody designs
Acute attention to details, well-organized, diligent with documentation
Highly goal-driven and displays the ability to handle delicate experiments in a timely manner
Able to operate in a collaborative environment and communicate clearly and concisely, both verbally and in the form of written reports
Benefits
Our client is an equal opportunity employer and value diversity at their company. They do not discriminate on the basis of race, religion, color, national origin, gender, s*xual orientation, age, marital status, veteran status, or disability status

05/12/2021

We are looking for a Senior/Principal Statistical Programmer for various clients (CRO's/BioPharma companies). The individual is responsible for the creation and validation of statistical programming deliverables, including compliant SDTM and ADaM datasets, all associated submission deliverables, and the tables, figures, and listings as required for the analysis and reporting of clinical trial data. Additional responsibilities include the QC of junior-level programmer deliverables. The individual must have the ability to work independently as an effective and engaged team member in a fast-paced environment. Strong initiative and follow-through are essential for this job. The ability to maintain confidentiality and to operate in the role with the highest ethical standards and professionalism are required.

Responsibilities
Provide hands-on contributions to customer's statistical programming activities on their trials and projects in drug development
Implement standard clinical data solutions best practices from CRF design through data analysis and reporting
Create and validate SDTM and ADaM datasets, associated specifications, and associated submission deliverables in compliance with published industry standards and project/study-specific requirements
Contribute to activities like ADaM conversion and pooling, ISS/ISE, safety update reports, Adhoc and publication deliverables, etc.
Create and validate TFL output in compliance with study-specific requirements.
Communicate effectively with the related stakeholders
Develop and validate statistical programs to support the analysis and reporting of data from clinical and nonclinical studies in support of all corporate therapeutic program areas
Assist in the development of relevant procedures and processes to ensure that statistical programs are properly documented and validated according to generally recognized industry and regulatory standards
Support the preparation of clinical study reports, regulatory submissions, and annual DSUR and safety reports
Manage study deliverables ensuring that timelines are met and expected quality is attained
Liaise with Data Management and Biostatistics for database and dataset specifications, timelines, and quality requirements
Assist in the creation of automated, standard programming; SAS macros, and stored procedures as required
Contribute to departmental process improvements; SOPs and WIs

Qualifications
A Bachelor’s degree and a minimum of 7 years of experience working in the biotech/pharmaceutical environment are required. Preferred area of degree: computer science, data science, mathematics, or statistics major preferred. (an equivalent combination of experience and education may be considered)
Exceptional SAS programming skills and expertise in the development and implementation of statistical programming procedures and processes in a clinical development environment
Excellent interpersonal skills and problem-solving capabilities with the ability to work independently under minimal supervision
Demonstrated ability to take a leadership role in all statistical programming activities for a clinical project including supervising the work of junior programmers
Knowledge of regulatory requirements for dataset submissions (including SAS and CDISC standards) and relevant hands-on experience
Ability to communicate effectively within a multi-disciplinary project team to assess priorities and complete assigned tasks on time
Demonstrable expertise in SAS analysis and reporting programming
Demonstrable expertise with CDISC CDASH, SDTM, ADaM, DEFINE-XML, and/or controlled terminology

05/12/2021

We are seeking a talented and highly motivated computational biologist and bioinformatics scientist to build and enhance our client's drug positioning AI platform that can predict drug response, therapeutic benefit and survival outcome of cancer patients, and generate biomarkers for specific cancer types for a drug candidate of interest. Candidates must have a passion to solve world problems in cancer treatment using bioinformatics and computer science with involvement in optimizing the company's core bioinformatics workflows, computational algorithms, and AI-based algorithms to improve their level of robustness, effectiveness, and efficiency.

Responsibilities
Leveraging cutting-edge Machine Learning technology to develop clinically relevant AI platforms for discovery of drug-tumor-specific biomarkers
Designing biologically-meaningful optimization and validation strategies to assess the applicability and relevance of the set of biomarkers
Applying biomarkers to larger data sets and developing optimal approaches for patient stratification
Incorporating multi-omics (RNAseq, NGS, proteomics, mutation, methylation) data to the current workflow to strengthen the platform
Integrating systems biology and statistical analysis to identify druggable tumor signaling pathways
Assisting the data scientists to apply Machine Learning/Deep Learning algorithms on biological data
Identifying institutions/companies to collaborate with and get data access
Processing, analyzing, and interpreting high volumes of data for the development and validation of methods
Collaborating with other informatics scientists, academic experts, and statisticians around data analysis methods and solutions for automated workflows and database creation
Implementing, executing, and documenting bioinformatics pipelines and workflows
Publishing scientific papers and posters and presenting the platform and its findings effectively in conferences/meetings
Qualifications
Ph.D. in Bioinformatics, Biostatistics, Computational Biology, Computer Science or other related field or Masters degree with 3+ years of relevant experience
At least 2-3 years of experience in scripting languages like R, Perl & Python
Solid understanding and 2+ years of hands-on experience with statistics, data mining, machine learning, and statistical data modeling techniques
Familiarity with fundamental concepts in molecular biology, chemical biology, statistics, and bioinformatics
Acquiring a broad knowledge of multiple sectors in the life sciences and NGS technology
Experience using NGS data for one of the following: biomarker discovery, drug target identification, large cohort analysis, patient stratification
Demonstrating technical and thought leadership and ability to influence and guide the work of others
Excellent interpersonal and communication skills, with strong written and verbal presentation
Background in oncology or clinical experience
Familiarity with raw NGS data processing is highly preferred
Knowledge and experience of online bioinformatics analysis tools & software
Experience working with cloud computing
Must be able to work in a fast-paced and team-oriented environment
Benefits
Opportunity to work with a recent IPO company with a 10% bonus based on performance and stock options. The company provides multiple growth opportunities and as an early employee, your work will have a direct impact on precision oncology that can change the drug development and clinical trial model. In addition to attractive compensation, and benefits, the company offer perks like unlimited vacation/sick days, subsidized gym memberships, and global travel opportunities to leading conferences and industry trade show

Address

180 Harbor Drive
Sausalito, CA
94965

Telephone

+14155790549

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