Description
\t\t\t\t\tThis position is on-site full time in San Diego, CA. The candidate should have solid training and/or broad experiences in oncology clinical development. The candidate will work with clinical project teams to support medical aspects of the clinical programs, including medical monitoring, communication with principal investigators (PIs) on clinical trial sites, optimizing study designs, helping with data readout, reporting clinical trial data and presenting updates to the senior management. This candidate will also be a resource to teams on all matters related to analysis and communication of clinical data. In addition, the candidate is expected to be skillful in integrating information from various functions and be articulate in communicating company clinical development strategy to internal and external stakeholders. The candidate must be a team player and is expected to work with other scientific and clinical staff in executing the clinical programs. Compensation will be commensurate with experience and skillset.• Serve as a Study Medical Monitor, authoring clinical trial documents including protocols, investigator brochures, ICFs, training materials, and DSURs.• Provide clinical development support and scientific opinion to study teams.• Contribute to the development and optimization of clinical trial study designs.• Work closely with Clinical Operations to execute clinical trials with high quality, deliver results and meet target timelines.• Drive contribution of clinical content for deliverables in support of regulatory submission activities and ensure flow and accuracy of key data for clinical module sections of the IND.• Provide medical input for the clinical database build, CRFs, monitoring plan, data management plan, safety monitoring plan and statistical analysis plans.• Contribute to the ongoing scientific review of clinical trial data and assist with query generation/resolution and data analysis. Work closely with PV, Data Management, and other vendors to ensure appropriate review and documentation of clinical trial data.• Maintain scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment. Stay abreast of internal and external developments, trends, and other dynamics relevant to the work to maintain a fully current view.• Develop and maintain relationships with a variety of internal and external partners and stakeholders, including clinical investigators, study coordinators/CRAs and KOLs.• Review and manage clinical development budgets and provide forecasts to the clinical development and finance team members
\t\t\t\t\tSkills
\t\t\t\t\tOncology, medical degree, Biopharma
\t\t\t\t\tTop Skills Details
\t\t\t\t\tOncology,medical degree,Biopharma
\t\t\t\t\tAdditional Skills & Qualifications
\t\t\t\t\t1. Medical Degree (MD or DO) preferably board certified in medical oncology.2. 5+ years’ experience in clinical development with at least 2 years in the biopharmaceutical industry. Experience in translational medicine/early phase oncology clinical trials is a plus.3. Solid understanding of GCP/ICH/IRB and local regulatory authority drug research and development guidelines and regulations.4. Proven ability to interact and work with external partners (PIs and consultants) with regards to clinical development functions.5. A solid understanding of the clinical trial processes, such as study start up, patient recruitment and safety, non-compliance, management, and monitoring of investigative sites.6. Excellent problem-solving skills, a strong sense of urgency and keen attention to detail. Well organized with the ability to effectively manage multiple priorities in a dynamic, cross-functional teamwork environment under time and resource pressures.7. A proven track record of successfully working within a collaborative team environment and building positive relationships as an individual contributor is required.8. Excellent oral and written communication skills and strong organizational skills are required.9. Ability to adapt to modification and changes to project plans, demonstrating flexibility to implement new strategies and tactics to accommodate these changes
\t\t\t\t\tExperience Level
\t\t\t\t\tExpert Level
Pay and Benefits
The pay range for this position is $250000.00 - $330000.00
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)
Workplace Type
This is a fully onsite position in San Diego,CA.
Application Deadline
This position will be accepting applications until Jan 25, 2025.
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.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe 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.