... preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and ... Strong project management skills with demonstrated ability to manage projects and/or colleagues in ...
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... preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and ... Strong project management skills with demonstrated ability to manage projects and/or colleagues in ...
Preclinical Project Manager information
How does a preclinical project manager typically coordinate with cross-functional teams during a drug development project?
A Preclinical Project Manager works closely with scientists, regulatory affairs, toxicology, and external vendors to ensure all preclinical studies are executed on time and within budget. They facilitate regular meetings to align project milestones, address challenges, and manage documentation for compliance. Effective communication and proactive issue resolution are key, as the role often requires balancing the needs of diverse stakeholders while keeping the overall project timeline on track.
What are the key skills and qualifications needed to thrive as a preclinical project manager, and why are they important?
To thrive as a Preclinical Project Manager, you need a solid background in life sciences or pharmaceutical research, often with an advanced degree and experience managing preclinical studies. Familiarity with project management tools, regulatory guidelines (such as GLP), and software like Microsoft Project or similar platforms is typically required. Strong organizational, leadership, and communication skills are vital for coordinating cross-functional teams and ensuring project timelines are met. These skills and qualifications are crucial for efficiently advancing drug candidates through preclinical development while ensuring compliance and project success.
What does a preclinical project manager do?
A Preclinical Project Manager oversees the planning, coordination, and execution of preclinical research projects that typically involve laboratory and animal studies before clinical trials in humans can begin. They work closely with scientists, regulatory teams, and stakeholders to ensure that studies are conducted according to protocols, timelines, and regulatory requirements. Their responsibilities include managing budgets, resources, and communication among various teams to advance drug candidates or medical devices through the early stages of development. Effective Preclinical Project Managers help ensure that projects meet scientific and business objectives, and that all data generated is reliable and compliant with industry standards.
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What job categories do people searching Preclinical Project Manager jobs in Georgia look for? The top searched job categories for Preclinical Project Manager jobs in Georgia are:
Full-time
Re-posted 13 days ago
Job description
Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
We are seeking an experienced cardiometabolic Medical Science Liaison (MSL) to join an exciting opportunity within our Medical Affairs (MA) team and work in a dynamic and collaborative environment. This is a field-based position and the candidate must be located within one of the territories .
MSLs are responsible for developing professional relationships with healthcare professionals through scientific engagement to support clinical stage and launch molecules. MSLs engage healthcare professionals through scientific exchange and provide clinical and scientific support.
Responsibilities
- Engage with cardiologists / endocrinologists / healthcare professionals / stakeholders to educate on clinical and scientific evidence to advance treatment landscape as aligned with strategic imperatives.
- Educate on RNAi technology, hypertriglyceridemia, familial chylomicronemia syndrome, and hypercholesterolemia.
- Synthesize and communicate clinical and scientific insights to internal stakeholders.
- Attend and present at scientific congresses and meetings to stay up to date with the latest scientific developments and trends in cardiometabolic therapeutic area.
- Respond to unsolicited inquiries consistent with MSL compliance standards.
- Support company sponsored clinical trials through investigator site engagement.
- Support speaker training as requested and ensure speakers are up to date with evolving disease and product data.
- Support national, regional, and local scientific congresses including Opinion Leader (OL) engagement, session coverage, booth, and company debriefs.
- Monitor and analyze scientific publications, clinical trials, and competitive landscape in the cardiometabolic therapeutic area.
- Maintain clinical and scientific expertise and general industry business acumen.
- Advance MSL value proposition, demonstrate tact and professionalism, and deliver results.
- Act in accordance with company policies
- Develop territory specific OL and account plans including OL profiles, pre-call planning, and follow up plans.
- Communicate clinical and scientific information in an accurate and clear manner.
- Document MSL quantitative and qualitative accomplishments.
- Provide scientific support for Med Info inquiries, ensuring accurate and timely responses to healthcare professionals' queries.
- Develop scientific content for medical education initiatives.
- Support Medical Affairs as needed with special projects and initiatives.
- Sophisticated cross-functional relationship management is critical for success.
Requirements
- PhD, PharmD, MD, or DO degree required
- 5 years of experience as an MSL
- Cardiometabolic therapeutic experience
- Industry experience in Medical Affairs at a biotech or pharma
- High level verbal and written communication skills.
- Ability to effectively collaborate in a dynamic environment.
- Strong comprehension of cardiometabolic therapeutic area.
- Ability to interpret key scientific data and translate the findings to meet educational and research needs to affect corporate research strategic activities/decisions.
- Ability to identify the unmet medical, educational, and research needs at a local & regional level in the medical community.
- An understanding of the health care delivery system, including the managed care arena and its impact on patient care, regional medical care and the pharmaceutical industry.
- Understanding of the design and execution of research studies and strategic implications.
- Proven ability to drive results at a high level of quality as a strategic and creative thinker.
- Demonstrates ability to deal with ambiguity and thrive in an ever-changing environment.
- Strong project management skills with demonstrated ability to manage projects and/or colleagues in successful implementation of business-critical projects.
- Strong time management & organizational skills.
- Ability to travel.
Pay Range
$190,000—$210,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
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About Arrowhead Pharmaceuticals
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
201 - 500 Employees
Headquarters location
Pasadena, CA, US
Year founded
1989