... FDA submissions. • Monitor, perform data review, and summarize safety and efficacy data in ... Assist with study design for exploratory development. • Lead the clinical matrix teams for ...
Quick apply
... FDA submissions. • Monitor, perform data review, and summarize safety and efficacy data in ... Assist with study design for exploratory development. • Lead the clinical matrix teams for ...
Quick apply
... FDA submissions. • Monitor, perform data review, and summarize safety and efficacy data in ... Assist with study design for exploratory development. • Lead the clinical matrix teams for ...
Veterinary Research Scientist Primary Responsibilities: This position requires a broad knowledge of ... FDA, and AALAC) * Train staff on in-vivo procedures * Make recommendations and assist in ...
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Veterinary Research Scientist Primary Responsibilities: This position requires a broad knowledge of ... FDA, and AALAC) * Train staff on in-vivo procedures * Make recommendations and assist in ...
Your ability to plan research, contribute to publications, and assist in securing funding will be ... FDA guidelines and competency in pharmacokinetic data analysis. The candidate should be able to ...
Your ability to plan research, contribute to publications, and assist in securing funding will be ... FDA guidelines and competency in pharmacokinetic data analysis. The candidate should be able to ...
Philadelphia PA 19112 The Associate Scientist is a temporary position to assist the laboratory ... WGS, classic microbiology, Petrifilm analyses, FDA BAM confirmations, TEMPO and GeneUp technologies ...
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Philadelphia PA 19112 The Associate Scientist is a temporary position to assist the laboratory ... WGS, classic microbiology, Petrifilm analyses, FDA BAM confirmations, TEMPO and GeneUp technologies ...
Austin, TX · On-site
... * Assist in intellectual property development * Conform to applicable Design Control regulations ... Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (Low ...
Austin, TX · On-site
... * Assist in intellectual property development * Conform to applicable Design Control regulations ... Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (Low ...
... and assist in training new analysts on the first or second shift. Responsibilities * Perform ... Experience working within an FDA- and GMP-regulated laboratory setting. INTERESTED IN THIS ROLE?
Quick apply
... and assist in training new analysts on the first or second shift. Responsibilities * Perform ... Experience working within an FDA- and GMP-regulated laboratory setting. INTERESTED IN THIS ROLE?
... Assist the team in functional training initiatives. * Support global change control activities as ... Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare ...
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... Assist the team in functional training initiatives. * Support global change control activities as ... Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare ...
Branchburg, NJ · On-site
$78K/yr
... Assist the team in functional training initiatives. * Support global change control activities as ... Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare ...
Branchburg, NJ · On-site
$78K/yr
... Assist the team in functional training initiatives. * Support global change control activities as ... Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare ...
Fort Detrick, MD · Hybrid
$97K - $124K/yr
... * Assist the Government to develop policies, procedures, guidelines, and other materials to ensure ... Acquire and retain knowledge of current Federal, DoD, FDA, Army, state, host nation, and DHA ...
Fort Detrick, MD · Hybrid
$97K - $124K/yr
... * Assist the Government to develop policies, procedures, guidelines, and other materials to ensure ... Acquire and retain knowledge of current Federal, DoD, FDA, Army, state, host nation, and DHA ...
$97K - $124K/yr
... * Assist the Government to develop policies, procedures, guidelines, and other materials to ensure ... Acquire and retain knowledge of current Federal, DoD, FDA, Army, state, host nation, and DHA ...
$97K - $124K/yr
... * Assist the Government to develop policies, procedures, guidelines, and other materials to ensure ... Acquire and retain knowledge of current Federal, DoD, FDA, Army, state, host nation, and DHA ...
... Assist the team in functional training initiatives. * Support global change control activities as ... Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare ...
... Assist the team in functional training initiatives. * Support global change control activities as ... Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare ...
$29 - $39/hr
... and assist in training new analysts on the first or second shift. Responsibilities * Perform ... Experience working within an FDA- and GMP-regulated laboratory setting. INTERESTED IN THIS ROLE?
Quick apply
$29 - $39/hr
... and assist in training new analysts on the first or second shift. Responsibilities * Perform ... Experience working within an FDA- and GMP-regulated laboratory setting. INTERESTED IN THIS ROLE?
Madison, WI · On-site
$76K - $125K/yr
Position Overview The Core Scientist, Technical Transfer role will lead and assist a variety of ... FDA guidelines. * Assists execution of development batches per a defined build plan, assists ...
Madison, WI · On-site
$76K - $125K/yr
Position Overview The Core Scientist, Technical Transfer role will lead and assist a variety of ... FDA guidelines. * Assists execution of development batches per a defined build plan, assists ...
Chaska, MN · On-site
$105K - $115K/yr
Candidate should be able to assist in developing new techniques and procedures that lead to greater ... Candidate should have a willingness to work in an ISO9000/FDA regulated environment. This position ...
Chaska, MN · On-site
$105K - $115K/yr
Candidate should be able to assist in developing new techniques and procedures that lead to greater ... Candidate should have a willingness to work in an ISO9000/FDA regulated environment. This position ...
Chaska, MN · On-site
$105K - $115K/yr
Candidate should be able to assist in developing new techniques and procedures that lead to greater ... Candidate should have a willingness to work in an ISO9000/FDA regulated environment. This position ...
Chaska, MN · On-site
$105K - $115K/yr
Candidate should be able to assist in developing new techniques and procedures that lead to greater ... Candidate should have a willingness to work in an ISO9000/FDA regulated environment. This position ...
New York, NY · On-site
$100K - $136K/yr
Both assets have been granted Fast-Track Designation by the FDA. Volastra is also developing new ... We want a scientist who is excited to use modern AI coding assistants thoughtfully. AI should ...
New York, NY · On-site
$100K - $136K/yr
Both assets have been granted Fast-Track Designation by the FDA. Volastra is also developing new ... We want a scientist who is excited to use modern AI coding assistants thoughtfully. AI should ...
$120K - $150K/yr
Review laboratory records, procedures, and study data for completeness and accuracy. Assist in ... Follow Standard Operating Procedures (SOPs), ensure compliance with GLP, FDA's ICH M10 guidelines ...
Quick apply
$120K - $150K/yr
Review laboratory records, procedures, and study data for completeness and accuracy. Assist in ... Follow Standard Operating Procedures (SOPs), ensure compliance with GLP, FDA's ICH M10 guidelines ...
$100K - $136K/yr
... and assist in the authoring and reviewing technical regulatory submission documents ... Knowledge of relevant industry guidance for US and Global products and regulatory guidelines (FDA ...
$100K - $136K/yr
... and assist in the authoring and reviewing technical regulatory submission documents ... Knowledge of relevant industry guidance for US and Global products and regulatory guidelines (FDA ...
Waltham, MA · On-site
... * Assist Non-clinical Project Leaders in integrating and assembling toxicology data for regulatory ... Solid understanding of ICH, FDA, and EMA guidelines related to the nonclinical assessment of drug ...
Waltham, MA · On-site
... * Assist Non-clinical Project Leaders in integrating and assembling toxicology data for regulatory ... Solid understanding of ICH, FDA, and EMA guidelines related to the nonclinical assessment of drug ...
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Solid understanding and knowledge of general chemistry and separation science.
... • Assist in designing method validation or method transfer protocols and establish project ... FDA guidance • Solid understanding and knowledge of general chemistry and separation science.
$7.93 - $9.86
2% of jobs
$9.86 - $11.78
4% of jobs
$11.78 - $13.70
11% of jobs
$14.29 is the 25th percentile. Wages below this are outliers.
$13.70 - $15.63
24% of jobs
The median wage is $16.43 / hr.
$15.63 - $17.55
20% of jobs
$19.21 is the 75th percentile. Wages above this are outliers.
$17.55 - $19.47
16% of jobs
$19.47 - $21.39
6% of jobs
$21.39 - $23.32
4% of jobs
$23.32 - $25.24
1% of jobs
$25.24 - $27.16
8% of jobs
$27.16 - $29.09
3% of jobs
$7
$17
$29
$125/hr
Contractor
Medical, Dental, Vision, Life, Retirement, PTO
Posted 7 days ago
Oncology/Solid Tumors Director, Clinical Research Scientist (CS) Contractor
Scope of Services:
This position will be responsible for working with physicians, clinical scientists, and cross-functional teams within Oncology/Solid Tumors Clinical Development to
provide clinical research support, with an emphasis on protocol development and study start up activities while serving in the role of CS.
Essential Functions of the Job (Key responsibilities of the oncology CS)
• Development of protocols for clinical studies.
• Preparation of clinical development plans.
• Drafting of clinical scientific documents such as IND, IND amendments, Investigator’s Brochures, Annual Reports and other FDA submissions.
• Monitor, perform data review, and summarize safety and efficacy data in ongoing studies.
• Assist with study design for exploratory development.
• Lead the clinical matrix teams for assigned compounds.
• Represent exploratory development on project teams.
• Develop relationships with appropriate consultants.
• Write abstracts and present data at scientific meetings, both internally and externally.
• Serve as liaison to project teams, CROs and others
Qualifications
• Degree in a scientific/life sciences field; Pharm.D. or Ph.D. preferred.
• Minimum of 8 years of experience in oncology research or related field.
• Demonstrated experience leading clinical development programs in oncology (preferably late-stage).
• Experience with global regulatory interactions and submissions (FDA, EMA, or other agencies).
• Strong understanding of oncology clinical endpoints, trial design, and statistical considerations.
• Proven ability to work effectively in a cross-functional matrix environment and influence without direct authority.
• Track record of scientific publications and/or conference presentations.
• Excellent written and oral communication skills.
• Strong analytical and scientific writing skills.
• Ability to manage multiple priorities in a fast-paced environment.
• Minimal travel (≈15%) may be required with prior approval.
Job Type & Location
This is a Contract position based out of Wilmington, DE.
Pay and BenefitsThe pay range for this position is $125.00 - $125.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
This is a hybrid position in Wilmington,DE.
Application DeadlineThis position is anticipated to close on Jun 12, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
5,001 - 10,000 Employees
Hanover, MD, US
1983