Associate Director, Clinical Science

Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.  Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you're ready to join us at the edge of something unstoppable, let's make a profound impact together for our patients, for your career, for what's beyond. You can view our latest corporate deck and other presentations here. About the Role >>> Associate Director, Clinical Science As the 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 job contributes to and supports Olema's mission of developing therapies that offer the potential to improve outcomes for women living with cancer. This role may be based out of our San Francisco, CA or Cambridge, MA office and will require up to 15% travel. Your work will primarily encompass: Assisting in writing clinical documents including protocols, amendments, investigator's brochures, clinical study report (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 Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and/or individual subject safety Contributing to the writing and/or review product specific abstracts, publications and supporting the development of presentations for scientific meetings And will also 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 Operation 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 >>> Self-Motivated Clinical Scientist A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role. 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: Minimum 5-7+ years' experience working as a clinical scientist in the biotech/pharmaceutical industry Comprehensive knowledge of oncology clinical trial implementation and drug development process Demonstrated 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 urgencyDemonstrated success motivating both internal and external team members and collaborators, fostering and nurturing 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 The base pay range for this position is expected to be $200,000 - $215,000 annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits. #LI-CK1 Important Information >>> We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.Please note: Olema doesn't accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.Fraud Alert:  We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema's official email addresses end in Our official corporate website is ; our careers page is ; our LinkedIn page is  Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.