Job Details

Overview

Lead Talent Acquisition Partner at Olema Oncology

Olema Oncology is a cancer medicines company dedicated to impacting breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a differentiated oral medicine known as a complete estrogen receptor antagonist (CERAN) initially in development for metastatic breast cancer. Our pipeline also includes OP-3136, a potent, selective oral inhibitor of the KAT6 pathway. At Olema, we are building a focused team committed to our mission with intention and clarity. Working alongside a talented passionate group of leaders and advisors, we strive to create better medicines that aim to help patients feel better, longer. For more information, visit us at www.olema.com.

The role: Associate Director, Clinical Science. Reporting to the Director, Clinical Science, you will play a key role in one of our ongoing clinical studies. You will collaborate within a multi-disciplinary team—including Clinical Operations, Medical Monitors, Data Management, Biostatistics, Clinical Pharmacology, Regulatory, and Program Management—to plan, conduct, and analyze clinical trials. Your work will contribute to Olema's mission of developing therapies that offer the potential to improve outcomes for women living with cancer. This role may be based in San Francisco, CA or Cambridge, MA, and will require up to 15% travel.

Responsibilities

• Assisting in writing clinical documents including protocols, amendments, investigator's brochures, clinical study reports (CSR), and the clinical sections of regulatory documents
• Interacting with investigators and thought leaders in oncology to facilitate the design of clinical synopsis and protocols
• Participating in ongoing clinical data review in collaboration with a cross-functional team
• Ensuring trial implementation according to the protocol and analyzing information to assess issues relating to protocol conduct and/or individual subject safety
• Contributing to the writing and/or review of product-specific abstracts, publications and supporting the development of presentations for scientific meetings

Additional responsibilities include:

• Collaborating with Clinical Operations and other internal study teams to develop Informed Consent Forms, Case Report Forms and CRF instructions
• Collaborating with Clinical Operations and other team members to develop agendas, training materials and presentations for site visits, investigator meetings and other study-related activities
• Ensuring adherence to Olema's Standard Operating Procedures and values, and maintaining the highest level of ethical behavior by leading by example
• Maintaining clinical and technical expertise in the therapeutic area of oncology
• Attending scientific meetings pertinent to clinical science activities

Ideal Candidate Profile

Knowledge

• Advanced degree such as a PhD or PharmD; equivalent combination of relevant education and experience may also be considered
• Experience in oncology clinical development is required
• Ability to interact effectively within a cross-functional team

Experience

• 5-7+ years of experience as a clinical scientist in the biotech/pharmaceutical industry
• Comprehensive knowledge of oncology clinical trial implementation and drug development process
• Understanding of the clinical drug development process to execute drug development strategic plans and meet milestones
• Strong knowledge of Good Clinical Practices (GCP), FDA, and EMEA/CHMP regulations and guidelines; familiarity with other international regulatory requirements is a plus
• Ability to proactively identify challenges/problems and propose solutions with a strong sense of urgency
• Proven ability to motivate internal and external team members and foster teamwork

Attributes

• Strong attention to detail
• Excellent written and oral communication skills
• Ability to work in a diverse and dynamic cross-functional team
• Passionate about the drug-development process
• Self-starter who thrives in a fast-paced environment

Compensation

The base pay range for this position is $200,000 - $215,000 annually, with total compensation including equity, bonus, and benefits. Location, market, job-related knowledge, skills, capabilities, and experience may affect base pay.

Important Information

We provide equal opportunity to all employees and applicants for employment. Olema is building a culture where the value of difference is celebrated. A Summary of Benefits is available for all applicants. Olema does not accept agency resumes and is not responsible for fees related to unsolicited resumes.

Fraud Alert: Olema cautions about employment scams. Official Olema email addresses end in @olema.com. Our official site is olema.com; careers page olema.com/careers; LinkedIn page linkedin.com/company/olema-oncology. We do not conduct interviews via text, will not ask for upfront payments, and do not make offers without an in-person interview.

Seniority level

• Director

Employment type

• Full-time

Job function

• Research, Science, and Manufacturing

Industries

• Biotechnology Research and Pharmaceutical Manufacturing